11271017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: 111071009-A-G

http://identifiers.org/hco/11/GRCh38#11271036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111071032-C-A

http://identifiers.org/hco/11/GRCh38#11271087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111071087-A-C

11271087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: 111071087-A-G

11271119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: 111071119-G-T

11271126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: 111071126-G-A

11271126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: 111071126-G-T

11271132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3 prime UTR variant
orthologous variants: 111071132-G-A

http://identifiers.org/hco/11/GRCh38#11271304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111071303-C-A

11271304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071303-C-T

11271323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071325-G-A

11271323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071325-G-C

11271408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071397-A-T

11271429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071419-T-G

11271612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071593-G-A

11271667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071652-G-A

11271748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111071736-C-T

11280523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111072651-C-T

11280546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111072673-C-T

http://identifiers.org/hco/11/GRCh38#11280823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111072904-C-A

11280932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073013-G-A

11280932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073013-G-T

http://identifiers.org/hco/11/GRCh38#11280955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111073037-A-C

11280988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073069-C-T

11281036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073129-C-T

11281125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073215-A-G

11281496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073588-T-A

11281496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073588-T-G

11281520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073613-C-T

11281590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073670-G-A

11281590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073670-G-T

11281607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111073699-C-T

http://identifiers.org/hco/11/GRCh38#11281904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111073982-C-A

11281964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074020-G-A

11281964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074020-G-T

11282018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074063-G-T

11282176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074110-C-G

11282201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074127-T-C

http://identifiers.org/hco/11/GRCh38#11282295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111074208-C-A

11282429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074332-T-G

11282499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074401-G-C

http://identifiers.org/hco/11/GRCh38#11282794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111074708-C-A

11282794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074708-C-T

11282937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074851-C-T

11282938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074852-G-A

11283028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074939-G-A

11283105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111074972-A-G

11283375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075112-G-T

11283438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075121-T-A

11283473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075156-T-A

11283517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075201-G-A

11283564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075245-C-T

11283807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075535-C-T

11283812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075540-C-T

11283820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075548-G-A

11283895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075622-G-A

11284159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075883-G-A

11284188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075912-T-C

11284232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111075923-C-T

11284329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076059-C-T

11284376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076242-C-T

11284889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076709-T-C

http://identifiers.org/hco/11/GRCh38#11284905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111076726-C-A

11284905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076726-C-T

11285144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076919-G-A

11285172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076947-C-G

11285172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076947-C-T

11285221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076988-T-C

11285223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111076990-G-T

11285317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111077070-T-C

11285359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111077093-T-G

http://identifiers.org/hco/11/GRCh38#11285360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111077094-C-A

11285782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111077505-G-A

11286112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111077793-C-T

11286317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111077990-G-A

http://identifiers.org/hco/11/GRCh38#11286471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111078084-C-A

11286654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111078226-C-T

http://identifiers.org/hco/11/GRCh38#11286771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111078733-C-A

11286771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111078733-C-T

11286910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111078920-C-T

11286960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111078968-C-G

11286969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111078977-C-T

11286989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111078988-C-T

11287131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079088-C-T

11287224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079176-C-G

11287313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079255-G-A

11287313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079255-G-T

11287410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079337-G-A

11287436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079350-C-T

11287456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079369-A-G

11287508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079404-T-C

11287581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079474-C-T

11287863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079732-G-C

11287926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079796-A-G

11287990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079847-C-G

11287990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111079847-C-T

11288174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080180-C-T

11288201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080259-C-T

11288259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080429-C-T

http://identifiers.org/hco/11/GRCh38#11288441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111080624-A-C

11288458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080641-C-G

11288462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080645-C-T

11288502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080685-G-A

http://identifiers.org/hco/11/GRCh38#11288586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111080771-C-A

11288586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080771-C-T

11288612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080797-G-A

11288612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080797-G-C

11288671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080856-G-A

11288671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080856-G-C

11288763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080937-G-T

11288793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080967-T-C

11288793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111080967-T-G

11289060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111081240-A-G

11290079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082155-C-T

11290133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082193-G-A

11290157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082217-C-G

11290272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082331-A-G

http://identifiers.org/hco/11/GRCh38#11290393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111082445-C-A

11290395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082447-C-G

11290395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082447-C-T

11290495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082528-C-G

11290515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082562-G-A

11290634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082652-A-G

11290803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082765-T-A

11290848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082820-C-T

11290865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082833-G-A

11290935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111082897-G-A

11291045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083007-C-T

http://identifiers.org/hco/11/GRCh38#11291509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111083316-C-A

11291509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083316-C-T

11291560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083359-C-T

11291562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083361-G-A

11291951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083722-A-G

11292044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083780-G-A

11292062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083798-G-A

11292115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111083851-C-T

http://identifiers.org/hco/11/GRCh38#11292139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111083875-C-A

http://identifiers.org/hco/11/GRCh38#11293161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111084374-A-C

11293161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111084374-A-G

11293207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111084420-G-A

11294212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111085153-G-C

11294230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111085170-T-C

11294274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111085217-T-C

11295592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111085364-G-C

11295954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111085704-T-C

11295970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111085720-C-T

11296694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086701-C-G

11296745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086752-A-T

11296776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086788-A-G

11296807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086804-T-G

11296820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086817-A-G

11296833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086830-A-G

11296833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086830-A-T

11296915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086914-C-T

11296931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086941-G-T

11296943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111086953-C-T

11297132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111087148-T-A

11297139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111087155-T-C

11297423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111088127-G-A

11297423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111088127-G-C

11297423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111088127-G-T

11297549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111088252-G-A

11297809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111088506-G-C

11297911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 111088603-G-A

11297981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111088669-G-A

11298227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111088986-G-A

11298630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111089510-C-G

11298630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111089510-C-T

http://identifiers.org/hco/11/GRCh38#11298648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111089528-A-C

http://identifiers.org/hco/11/GRCh38#11298723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111089599-C-A

11298723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111089599-C-T

11300172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111090445-G-A

11300172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111090445-G-C

11300196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111090474-T-G

11300746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111090948-A-G

11300767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111090964-T-C

11301156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111091650-C-T

11301491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111091958-T-A

11301595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111092054-C-T

11301856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111092264-C-T

11302143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111092458-C-T

11302183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111092488-T-C

11305021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111093409-G-C

11305026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111093414-G-T

11305240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111093554-G-A

11305316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111093629-G-A

11305380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111093708-C-T

11305693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111094008-A-G

11306008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111094247-T-C

11306121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111094372-C-G

11310137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111094900-G-A

11310184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111094943-C-T

11310448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111095199-T-C

http://identifiers.org/hco/11/GRCh38#11310749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111095495-C-A

11311095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111095822-G-C

11311114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111095842-G-A

11311182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111095887-T-A

11311214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111095905-A-T

11311226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111095916-C-G

11313790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096215-T-C

11313808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096233-A-G

11313813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096238-G-C

http://identifiers.org/hco/11/GRCh38#11313843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111096263-A-C

11313934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096378-G-A

11314018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096424-G-A

11314157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096567-C-G

11314320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096726-G-A

11314320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096726-G-T

11314352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096755-A-G

11314401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096799-G-A

11314401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096799-G-T

11314405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111096803-G-T

http://identifiers.org/hco/11/GRCh38#11314600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111096985-A-C

11314747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097142-T-C

11314773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097156-G-A

11314781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097164-A-G

11314791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097173-G-A

11314802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097190-T-C

11314810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097198-C-T

11314811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097199-T-C

11314825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097213-T-C

11314827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097215-C-T

11314851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097231-C-T

11315189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111097493-T-C

http://identifiers.org/hco/11/GRCh38#11316194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111098663-A-C

11316194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111098663-A-G

11316221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111098701-C-T

11316281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111098761-A-T

11316428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111098908-G-A

http://identifiers.org/hco/11/GRCh38#11316458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111098938-A-C

11316512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111099614-T-C

11316512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111099614-T-G

11316608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111099707-A-G

11316657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111099753-T-A

11316694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111099786-G-C

11316896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111099957-C-G

11317306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111100355-A-G

11317710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111100581-C-G

11318052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111100840-C-T

11318053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111100841-G-A

11318072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111100860-A-G

http://identifiers.org/hco/11/GRCh38#11318198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111100977-C-A

11318198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111100977-C-T

11318251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101038-G-C

11318295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101082-G-A

11318295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101082-G-C

11318363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101155-T-A

11318363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101155-T-C

11318364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101156-G-A

11318500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101260-T-C

11319020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111101929-C-T

http://identifiers.org/hco/11/GRCh38#11319661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111102387-C-A

11319749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111102391-C-T

11319922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111102515-T-C

11319972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111102564-T-C

11319990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111102582-G-A

11320011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111102603-C-G

11320073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111102621-T-C

11320264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111103411-C-T

11320332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111103478-G-A

11320670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111103740-T-C

11321154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111104148-G-T

http://identifiers.org/hco/11/GRCh38#11321282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111104276-C-A

11325753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106315-A-T

11325760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106320-T-G

11325962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106516-T-C

http://identifiers.org/hco/11/GRCh38#11326464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111106687-C-A

http://identifiers.org/hco/11/GRCh38#11326483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111106706-C-A

11326483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106706-C-T

11326485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106708-T-G

11326547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106769-T-C

11326622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106839-T-C

11326735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111106916-C-T

http://identifiers.org/hco/11/GRCh38#11326764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111106970-C-A

11326793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107000-C-T

11326835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107043-C-G

11326877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107084-C-T

11327008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107184-G-A

11327019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107195-G-C

11327019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107195-G-T

http://identifiers.org/hco/11/GRCh38#11327031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111107207-C-A

11327031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107207-C-G

11327031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107207-C-T

http://identifiers.org/hco/11/GRCh38#11327061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111107234-C-A

11327061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107234-C-T

11327237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107411-T-G

11327240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107414-A-G

11327245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107419-C-G

11327245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107419-C-T

11327283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107456-G-A

11327283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107456-G-T

http://identifiers.org/hco/11/GRCh38#11327310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111107483-C-A

11327601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107779-G-A

11327695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107874-T-C

11327769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111107917-T-C

11327910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111108061-T-C

11328308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111108436-T-A

11328308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111108436-T-C

11328446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111108588-C-T

11328810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111108729-T-C

11329009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111108896-G-T

11329119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111109007-A-G

11329435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111109291-C-T

11329502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111109377-T-C

11329528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111109432-T-C

11329676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111109796-G-A

11329882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111109993-C-G

11330173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111110263-G-A

11330358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111110456-C-T

11330455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111110535-C-T

11330498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111110584-G-A

11330532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111110618-G-A

11330741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111110818-C-T

http://identifiers.org/hco/11/GRCh38#11330824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111110905-A-C

11330930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111009-A-G

http://identifiers.org/hco/11/GRCh38#11330943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111111021-C-A

11330943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111021-C-T

11331049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111116-C-T

11331116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111169-T-G

http://identifiers.org/hco/11/GRCh38#11331132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111111184-C-A

11331263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111304-T-C

http://identifiers.org/hco/11/GRCh38#11331409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111111424-A-C

11331465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111465-A-G

11331513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111515-C-T

11331527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111529-G-A

11331672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111666-T-C

11331906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111868-C-G

11331945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111111911-G-A

11332059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112002-G-T

11332217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112226-A-T

11332319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112317-G-A

11332484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112490-G-A

11332484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112490-G-T

11332555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112562-A-G

11332567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112574-C-G

11332567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112574-C-T

11332612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112616-G-A

11332612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112616-G-C

11332612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112616-G-T

11332618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112622-T-A

11332641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112653-A-G

11332658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112670-T-C

11332660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112672-T-A

11332660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112672-T-C

11332685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112696-G-A

11332730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: 111112741-C-G

11332897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112945-T-C

11332897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112945-T-G

11332946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112999-G-A

11332946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111112999-G-T

http://identifiers.org/hco/11/GRCh38#11332948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111113001-C-A

11332948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113001-C-T

11332950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113003-A-G

11332950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113003-A-T

11335081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113207-G-C

http://identifiers.org/hco/11/GRCh38#11335165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111113291-C-A

11335176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113302-T-C

11335209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113323-G-A

11335209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113323-G-C

11335370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113667-A-G

11335470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113759-T-C

11335554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111113842-A-T

11335746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111114001-T-G

11335759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111114014-G-A

11335821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111114072-T-A

11335990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111114247-C-T

http://identifiers.org/hco/11/GRCh38#11336019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111114274-A-C

11336019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111114274-A-G

11336811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111114997-C-T

11336999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115175-G-A

http://identifiers.org/hco/11/GRCh38#11337144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111115296-C-A

11337287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115441-G-A

11337287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115441-G-T

11337466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115606-G-C

11337466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115606-G-T

11337518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115657-T-G

11337567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115698-G-A

11337675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111115801-T-A

11339340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111117585-A-G

11339427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111117641-G-A

11339738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111117899-G-T

11339753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111117909-C-T

11339763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111117919-T-C

http://identifiers.org/hco/11/GRCh38#11339790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111117950-C-A

11340292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111118491-C-G

11340292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111118491-C-T

11340610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119018-A-G

11340751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119127-G-T

11340769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119150-T-C

http://identifiers.org/hco/11/GRCh38#11341008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111119386-C-A

11341008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 111119386-C-T

11341019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119397-G-A

11341019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119397-G-C

11341037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119408-T-A

11341037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119408-T-C

http://identifiers.org/hco/11/GRCh38#11341152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111119515-A-C

11341152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119515-A-G

11341424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119788-C-G

11342355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111119914-C-G

11342447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111120000-G-C

11342910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111120429-C-T

11343467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111120652-G-A

11343693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111120874-T-C

11344013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121043-G-A

11344597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121405-C-T

11344791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121588-C-G

11344792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121589-T-C

11345037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121760-C-T

11345199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121906-T-C

11345242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111121949-A-G

11345415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111122108-C-T

11346318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111124694-G-C

11346461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111124829-C-G

11346461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111124829-C-T

11346717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111125078-G-A

11346725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111125086-G-C

11346950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111125310-G-A

11347143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111125497-C-T

11347226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111125575-C-T

11347542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126370-A-G

11347659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126464-T-C

11347677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126482-C-T

11347760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126565-T-C

11347863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126671-C-T

11347964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126763-G-A

11348045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126860-A-G

11348493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111126962-T-A

11348692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111127153-A-G

11349247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111127866-C-G

11349247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111127866-C-T

http://identifiers.org/hco/11/GRCh38#11349816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111128812-A-C

11350169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129119-C-T

11350458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129334-A-G

11350699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129469-G-A

11350734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129503-C-G

http://identifiers.org/hco/11/GRCh38#11350857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111129626-C-A

11350857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129626-C-T

11351013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129753-G-A

11351107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129818-G-A

11351165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111129876-T-G

11351362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111130065-G-A

11351457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111130147-C-G

11351530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111130221-G-T

http://identifiers.org/hco/11/GRCh38#11353454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111130538-C-A

11353454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111130538-C-G

http://identifiers.org/hco/11/GRCh38#11353462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111130549-C-A

11353807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111130913-C-T

11353957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111131031-C-T

11354243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111131796-T-A

11354284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111131824-C-T

http://identifiers.org/hco/11/GRCh38#11354466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111131989-C-A

11354483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, stop_retained_variant
orthologous variants: 111132006-C-T

11354714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111132228-C-T

11354796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111132308-C-T

11354979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111132531-T-C

11354979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111132531-T-G

http://identifiers.org/hco/11/GRCh38#11354999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111132551-C-A

http://identifiers.org/hco/11/GRCh38#11356400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111133802-C-A

11356407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111133812-C-T

11356432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111133836-G-A

11356489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111133895-T-C

11356693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111134123-G-A

11357181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111134575-C-T

11357223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111134618-G-T

11357328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111134753-C-T

11366653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111137942-G-C

11366696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138072-C-T

11366793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138314-C-T

11366888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138406-G-C

11367052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138560-C-G

11367071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138581-C-T

11367074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138584-G-C

11367140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111138636-C-T

11367574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111139232-G-A

11367591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111139249-C-T

11367630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111139281-C-T

11367661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111139293-A-G

11367992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111139539-A-G

11368953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144174-C-T

11369283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144446-A-T

11369285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144448-A-G

11369338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144497-T-A

11369414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144566-T-C

11369432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144583-G-T

11369575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144732-G-A

11369592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144752-G-T

11369599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111144761-G-A

11370031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145186-T-G

11370122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145275-G-A

11370216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145742-A-G

11370359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145890-C-G

11370359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145890-C-T

11370377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145908-T-G

11370420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145940-G-A

11370420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111145940-G-C

11370507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111146023-T-C

11370528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111146044-C-T

11370677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111146187-G-T

11371160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 111146667-C-T

11371401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111146888-T-C

11371416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111146903-G-A

11371460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111146934-G-A

11371580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147051-A-G

11371998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147397-G-A

11371998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147397-G-C

11372029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147428-T-G

11372189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147572-G-A

11372189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147572-G-C

11372365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147704-T-A

11372365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147704-T-C

11372365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147704-T-G

http://identifiers.org/hco/11/GRCh38#11372376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111147715-C-A

11372376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147715-C-G

http://identifiers.org/hco/11/GRCh38#11372385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111147724-C-A

11372419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147759-T-G

11372420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147760-G-C

11372420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147760-G-T

11372449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111147816-C-T

11372750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111148106-T-C

http://identifiers.org/hco/11/GRCh38#11372755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111148111-C-A

11372765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111148123-G-A

11372765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111148123-G-T

http://identifiers.org/hco/11/GRCh38#11374352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111149763-C-A

11374834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111150381-A-G

11375118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111150794-T-A

11375143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111150813-T-C

11375302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111150964-C-T

11375629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111151292-G-A

11376003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111152626-T-A

http://identifiers.org/hco/11/GRCh38#11376518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111152802-C-A

11376522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111152806-G-A

11376546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111152830-T-C

11376753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153012-G-A

11376776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153034-C-T

11376894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153110-A-T

11377097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153581-A-G

11377125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153591-G-T

11377140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153606-G-A

11377140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153606-G-T

11377310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: 111153774-G-C

11377331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: 111153795-G-C

http://identifiers.org/hco/11/GRCh38#11377399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111153866-C-A

11377399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153866-C-T

http://identifiers.org/hco/11/GRCh38#11377400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111153867-C-A

11377486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111153925-T-C

11377910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111154250-C-T

11378098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111154441-G-C

11378098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111154441-G-T

11378145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111154488-A-G

11378274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111154618-G-A

http://identifiers.org/hco/11/GRCh38#11378304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111154648-C-A

11378629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111154942-C-T

11378735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155053-T-C

11378837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155190-C-T

http://identifiers.org/hco/11/GRCh38#11378943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111155417-C-A

11378943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155417-C-T

http://identifiers.org/hco/11/GRCh38#11378965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111155439-C-A

11378965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155439-C-T

11379101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111155573-G-A

11379101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: 111155573-G-T

11379142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: 111155614-T-C

11379149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111155621-A-G

11379200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111155672-G-A

http://identifiers.org/hco/11/GRCh38#11379330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111155795-C-A

11379330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155795-C-T

11379371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155843-G-A

11379371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155843-G-T

11379412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155882-G-T

11379425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111155895-G-T

11379611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111156058-C-T

11379633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111156079-C-T

11381465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111156743-G-T

11381682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111156898-C-T

11381750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111156945-T-C

11381917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157127-G-C

11381917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157127-G-T

11381938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157138-T-A

11382089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157265-G-A

11382273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157476-T-C

11382327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157529-G-A

11382591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111157773-A-T

11382790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111158085-C-G

11382871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111158342-A-T

http://identifiers.org/hco/11/GRCh38#11382987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111158458-A-C

11382987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111158458-A-G

http://identifiers.org/hco/11/GRCh38#11383434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111158843-A-C

11383576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111158985-C-T

11387255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160252-T-C

11387328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160337-C-T

11387762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160717-G-A

11387794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160735-T-C

11387796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160737-G-T

http://identifiers.org/hco/11/GRCh38#11387896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111160830-C-A

11387896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160830-C-G

11387946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111160883-T-C

11388178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111161172-C-T

11388348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111161336-T-C

11388531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111161496-T-A

11388531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111161496-T-C

11388532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111161497-G-C

http://identifiers.org/hco/11/GRCh38#11388588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111161566-C-A

11390516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111162667-C-T

11390780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111162941-G-A

11393176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111165302-G-A

11393223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111165341-G-T

11393290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111165441-G-A

11393300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111165451-C-T

11393310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111165461-G-A

11393336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111165500-C-T

http://identifiers.org/hco/11/GRCh38#11393937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111166118-A-C

11393937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166118-A-G

11394040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166218-A-G

http://identifiers.org/hco/11/GRCh38#11394118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111166373-A-C

11394118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166373-A-G

http://identifiers.org/hco/11/GRCh38#11394160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111166407-A-C

11394211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166455-A-G

11394431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166761-G-A

11394431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166761-G-C

11394475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166805-C-T

http://identifiers.org/hco/11/GRCh38#11394527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111166850-C-A

11394527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166850-C-T

http://identifiers.org/hco/11/GRCh38#11394550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111166873-C-A

11394683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166987-C-G

11394683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111166987-C-T

11394810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167082-T-C

11394810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167082-T-G

11394880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167141-A-G

11395002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167250-A-G

11395208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167449-T-C

11395248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167487-G-C

11395671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167832-G-T

11395824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111167951-T-C

11396132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111168192-T-C

11396338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111168393-A-G

11396368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111168436-T-A

11396472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111168560-C-T

11396607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111168675-T-C

11397037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111169082-G-C

http://identifiers.org/hco/11/GRCh38#11397064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111169109-C-A

11397079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111169194-T-C

11397079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111169194-T-G

http://identifiers.org/hco/11/GRCh38#11397808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111169957-A-C

11397831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111169980-C-T

11397966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111170117-G-C

11397986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111170136-A-G

11402016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111171382-G-A

11402163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111171492-G-T

11402213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111171542-G-A

11402607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111171903-C-T

http://identifiers.org/hco/11/GRCh38#11402634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111171930-A-C

11402646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111171942-C-T

11402739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111172032-C-T

11403050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111172829-T-G

11403066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111172845-A-G

11403166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111172939-C-T

11403537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111173302-T-C

11403649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111173352-T-C

11403711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111173386-G-A

11403737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111173412-C-T

11403773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111173470-C-T

11403959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111173607-G-A

11404408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111174068-T-C

11404546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111174192-G-A

11404637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111174272-C-T

11404765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111174361-C-T

11404982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111174563-G-A

11405010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111174583-C-T

11405056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111174617-T-C

http://identifiers.org/hco/11/GRCh38#11405760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111175356-A-C

11405833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111175428-C-T

11406290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111176687-C-T

11406432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111176799-T-C

11406579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111176942-G-T

11406646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177015-G-A

11406786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177147-A-T

11406790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177151-G-A

11406844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177204-T-C

11406973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177347-C-T

http://identifiers.org/hco/11/GRCh38#11407070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111177439-A-C

11407141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177511-G-T

11407192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177571-G-T

11407246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177634-C-T

11407255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177640-C-T

11407340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177724-A-G

11407437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177822-C-T

11407470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177855-A-G

11407567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111177951-A-G

11407643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178027-G-A

11407643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178027-G-C

11407643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178027-G-T

11407771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178144-A-G

http://identifiers.org/hco/11/GRCh38#11407808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111178183-C-A

11407808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178183-C-T

11407809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178184-G-A

11407809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178184-G-C

11407850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178218-A-G

11407876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178237-G-A

11407876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111178237-G-C

11408618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179119-G-A

11410086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179269-A-G

11410116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179292-C-G

11410192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179391-C-T

11410260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179457-C-T

11410358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179567-G-A

11410366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179575-C-T

11410391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179594-T-G

11410519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179720-G-A

11410556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179757-G-T

11410641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111179841-A-G

11410893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111180073-A-G

11411039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111180262-G-A

http://identifiers.org/hco/11/GRCh38#11411449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111180507-C-A

11411454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111180512-T-C

11411848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111180868-G-A

11411875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111180893-C-T

http://identifiers.org/hco/11/GRCh38#11412062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111181050-A-C

11412063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111181051-A-G

11412121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111181106-C-T

11412348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111181331-C-T

11412357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111181343-G-A

11412520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111181494-C-T

http://identifiers.org/hco/11/GRCh38#11412654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111181629-C-A

11413547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111183336-G-A

11413596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111183381-T-A

11415242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111183919-G-A

11415587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184214-C-T

11415720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184353-C-T

11415726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184359-C-T

11415750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184431-C-T

11415831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184553-C-T

11415966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184687-C-T

11416074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184806-C-T

11416195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184910-T-C

11416239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184954-T-C

11416276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111184991-A-G

11416317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185031-T-C

http://identifiers.org/hco/11/GRCh38#11416403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111185118-C-A

11416559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185274-G-T

11417253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111185496-C-G

11417361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185602-C-T

11417526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185741-G-A

11417574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185774-G-C

11417634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185835-G-A

11417665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185866-T-G

11417720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185925-G-C

11417742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111185942-G-A

http://identifiers.org/hco/11/GRCh38#11420062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111186270-A-C

11420287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111186447-G-A

11420529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111186657-C-T

11420806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111187672-G-T

11420916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111187790-C-G

11420916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111187790-C-T

11421190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111188042-G-C

11421460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111188266-A-T

11422427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111189486-C-T

11422596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111189669-A-T

11422958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111189998-G-A

11422958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111189998-G-C

http://identifiers.org/hco/11/GRCh38#11423145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111190147-C-A

11423158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190160-A-G

11423234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190231-G-A

11423503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190441-T-C

11423531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190465-C-T

11423777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190682-C-T

11423836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190743-T-A

11423928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190832-G-A

http://identifiers.org/hco/11/GRCh38#11423932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111190836-A-C

11423944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190855-G-A

11424150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111190920-G-T

http://identifiers.org/hco/11/GRCh38#11424248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111191030-C-A

11424307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191088-T-C

11424403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191156-G-A

11424758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191457-C-T

11424862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191521-C-T

http://identifiers.org/hco/11/GRCh38#11424878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111191526-A-C

11424932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191587-G-A

11424984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191624-G-A

11425053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111191660-C-T

http://identifiers.org/hco/11/GRCh38#11425064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111191674-C-A

11425154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111192153-G-C

11425329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111192310-G-A

11425378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111192357-G-T

11425461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111192442-T-A

11426660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193068-A-G

11426722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193128-G-A

11426853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193224-G-A

11427131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193333-A-G

11427133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193334-C-T

11427231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193425-A-T

11427235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193429-C-T

11427237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193431-G-A

11427275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193463-G-C

11427324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193506-C-T

11427410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193551-G-A

11427428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193565-G-A

11427435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193572-C-T

11427668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193783-T-A

11427686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111193801-C-T

11427855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111193970-T-C

11427903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194018-G-A

11428108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194152-C-T

11428589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194517-T-C

11428728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194665-T-C

11428729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194666-G-A

11428756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194693-C-T

http://identifiers.org/hco/11/GRCh38#11428761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111194695-A-C

11428783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194715-T-G

http://identifiers.org/hco/11/GRCh38#11428784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111194716-A-C

11428856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194793-G-A

11428856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194793-G-C

11428930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111194873-G-T

11429367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111195318-T-A

11429424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111195371-C-T

11429429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111195376-C-G

11429429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111195376-C-T

11429614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111195518-T-A

11429718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111195614-T-C

11430228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196077-T-C

11430307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196166-G-A

11430307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196166-G-T

11430709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196546-A-G

11430897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196720-G-A

11430932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196755-G-A

11430932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196755-G-C

11431196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196964-T-C

11431215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111196984-T-C

11431235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197004-C-G

11431377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197064-G-T

11431392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197079-G-A

11431515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197198-G-A

11432073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197708-A-G

11432163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197783-C-T

11432204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197798-C-T

11432228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197816-C-T

11432379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111197951-T-G

http://identifiers.org/hco/11/GRCh38#11432446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111197997-A-C

11432502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198045-G-A

11432502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198045-G-T

11432554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198101-G-A

11432554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198101-G-C

11432554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198101-G-T

11432601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198145-T-A

11432601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198145-T-C

11432601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198145-T-G

11432688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111198231-C-T

11432883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198431-G-C

11432883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111198431-G-T

http://identifiers.org/hco/11/GRCh38#11432937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111198502-C-A

11433183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111199348-T-C

11433381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111199498-C-G

11433566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111199758-C-T

11433870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111200039-G-A

11433870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111200039-G-C

http://identifiers.org/hco/11/GRCh38#11434594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111200746-C-A

11434864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111200960-G-T

11434915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201015-G-C

11434970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201065-T-C

11435293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201525-C-T

11435372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201569-C-G

11435376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201573-G-A

http://identifiers.org/hco/11/GRCh38#11435553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111201687-C-A

11435569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201705-A-G

11435610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111201735-C-T

11435980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111202015-G-A

11436009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111202028-C-T

11436016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111202035-T-C

11436433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111202619-G-A

11436537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111202727-C-T

11436647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111202836-A-G

11436893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111203245-G-C

11436953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111203302-C-T

11436961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111203310-T-C

11437074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204378-C-T

11437232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204532-A-G

11437232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204532-A-T

11437263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204563-T-C

11437368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204663-G-A

11437470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204767-T-C

11437505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204802-T-C

11437528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204835-G-A

11437540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204847-T-C

11437557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204861-G-A

11437682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111204977-C-T

11438003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111205246-C-T

11438347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111205595-C-T

11438503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111205739-C-T

11438799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111206004-T-C

11439202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111206779-G-A

11439226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111206802-G-A

11439327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111206889-G-C

http://identifiers.org/hco/11/GRCh38#11439441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111206951-A-C

11439912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111207394-A-G

11440084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111207554-G-C

11440189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111207645-A-G

http://identifiers.org/hco/11/GRCh38#11440265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111207723-C-A

11440265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111207723-C-T

http://identifiers.org/hco/11/GRCh38#11440283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111207741-C-A

11440366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111207833-G-A

http://identifiers.org/hco/11/GRCh38#11440398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111207864-C-A

11440424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111207890-T-A

11440425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111207891-G-C

11440484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208180-G-A

http://identifiers.org/hco/11/GRCh38#11440644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111208384-C-A

11440828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208568-A-G

11440958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208702-A-T

11441089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208807-C-T

11441161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208878-T-C

11441200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208914-A-G

11441204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208918-T-C

http://identifiers.org/hco/11/GRCh38#11441220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111208934-C-A

11441220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208934-C-G

11441220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208934-C-T

11441229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208943-T-C

11441244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208958-G-C

11441279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111208993-A-G

11441360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111209078-T-C

11441471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111209177-G-A

11441471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111209177-G-C

11441473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111209179-T-A

11442764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111210428-G-T

11442765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111210429-C-T

11443113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111210757-G-A

11443179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111210803-C-G

http://identifiers.org/hco/11/GRCh38#11443257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111210878-C-A

11443359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111210979-C-T

11443447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211055-C-T

11443521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211098-G-C

11443678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211235-A-T

11443703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211260-G-A

11443956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211431-A-G

http://identifiers.org/hco/11/GRCh38#11444156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111211512-C-A

11444450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211697-G-A

11444632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111211843-G-T

11445243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212190-T-A

11445303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212250-T-C

11445351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212294-T-G

11445464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212402-T-C

11445582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212469-C-G

11445603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212489-G-T

http://identifiers.org/hco/11/GRCh38#11445657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111212526-C-A

11445740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212608-A-T

11445841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111212696-G-A

11448194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215043-A-G

11448272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215119-G-A

11448279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215126-T-A

11448410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215267-A-G

11448613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215406-G-A

11448613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215406-G-T

11448683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215449-T-C

http://identifiers.org/hco/11/GRCh38#11448684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111215450-C-A

11448684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215450-C-G

http://identifiers.org/hco/11/GRCh38#11448697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111215462-C-A

11448697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215462-C-T

11448717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215474-A-G

11448720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215477-G-A

11448720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215477-G-C

11448720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215477-G-T

http://identifiers.org/hco/11/GRCh38#11448770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111215525-C-A

11448779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111215534-G-A

11448905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111215660-G-A

11448905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111215660-G-C

11448905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111215660-G-T

http://identifiers.org/hco/11/GRCh38#11448914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111215669-C-A

11448914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: synonymous variant
orthologous variants: 111215669-C-T

11448964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215720-G-T

11448970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215726-G-A

11448970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215726-G-C

11448970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215726-G-T

11449059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215791-C-T

11449071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215803-G-T

11449198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111215929-A-G

11449339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111216054-C-T

11449799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111216369-A-T

11450649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111216976-C-G

11450653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111216980-G-A

11450715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111217038-T-C

11450731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111217054-G-A

11450899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111217180-G-C

11450906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111217191-C-T

11451074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111217377-G-A

11451074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111217377-G-T

11451117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, undefined
orthologous variants: 111217413-G-A

11454214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111218842-G-C

11454271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111218891-G-A

11454878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111219484-A-G

11454982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111219573-G-A

11454982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111219573-G-T

11455101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111219698-C-T

11456287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111220509-G-A

11456498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111220688-C-T

11456607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111220805-G-C

11456618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111220816-A-G

11456656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111220990-T-C

11456679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221017-G-A

11456840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221161-A-G

http://identifiers.org/hco/11/GRCh38#11456842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111221163-A-C

11456887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221203-T-C

11457362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221543-C-T

11457507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221659-A-G

11457635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221759-G-T

11457975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111221989-A-G

11458108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222114-G-A

11458139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222145-A-G

11458232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222233-T-C

11458232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222233-T-G

11458375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222556-T-C

11458555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222743-C-G

11458805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111222950-T-C

11461008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223652-T-C

11461010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223653-C-T

11461032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223675-G-A

11461040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223697-G-C

11461091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223732-G-A

11461107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223747-A-G

11461108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223748-C-T

11461358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111223983-G-T

11461386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111224011-C-T

11461388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111224013-T-C

11461436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111224062-A-G

11461629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111224245-T-C

11461632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111224248-T-C

11463554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111225109-C-G

11463554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111225109-C-T

http://identifiers.org/hco/11/GRCh38#11463734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111225235-C-A

11463865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111225369-C-T

11464084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111225598-G-T

11464134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111225648-T-C

11464406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226235-G-A

11464458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226239-T-C

http://identifiers.org/hco/11/GRCh38#11464479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111226260-A-C

11464479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226260-A-T

11464481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226262-G-A

11464509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226290-G-A

11464517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226297-G-A

11464882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226652-G-C

11464955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226720-C-G

11465150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111226901-T-C

http://identifiers.org/hco/11/GRCh38#11466204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111227607-C-A

http://identifiers.org/hco/11/GRCh38#11466293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111227659-A-C

http://identifiers.org/hco/11/GRCh38#11466380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111227738-C-A

11466898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228130-G-A

11466898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228130-G-T

11466953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228190-G-T

11466999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228234-C-G

11466999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228234-C-T

11467171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228381-G-A

11467234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228441-G-A

11467256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228463-A-G

11467330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228514-T-G

11467332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228516-C-T

11467492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228640-G-A

11467727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228981-C-T

11467734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228988-G-C

11467734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111228988-G-T

11467827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229063-T-C

11467827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229063-T-G

11467882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229101-T-C

11467906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229125-G-A

11468047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229242-T-C

http://identifiers.org/hco/11/GRCh38#11468110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111229286-C-A

11468166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229342-G-T

11468188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229364-T-G

11468347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229530-G-C

11468604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229729-G-C

11468609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229734-T-C

11468710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229817-G-A

11468712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111229823-G-A

http://identifiers.org/hco/11/GRCh38#11469252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111230247-C-A

11469323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111230316-A-T

11469332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111230325-C-G

11469332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111230325-C-T

11471723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111232272-C-T

11471981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111232513-G-A

11472172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111232684-C-T

11472523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111233024-A-G

11472948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111233410-A-T

11472969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111233474-A-G

11473173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron variant
orthologous variants: 111233673-A-G

11473281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111233786-G-C

11473444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111233948-T-A

11473513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234016-A-G

11473570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234073-G-A

http://identifiers.org/hco/11/GRCh38#11474147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111234353-A-C

11474147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234353-A-G

11474195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234403-G-C

11474195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234403-G-T

11474237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234434-G-T

11474239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234436-G-A

http://identifiers.org/hco/11/GRCh38#11474244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111234441-C-A

11474387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234592-G-A

11474509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234711-T-C

11474547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234756-G-A

11474657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111234872-G-A

11475177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111235761-T-C

11475177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111235761-T-G

http://identifiers.org/hco/11/GRCh38#11475219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111235808-C-A

11475452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236040-G-A

11475452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236040-G-T

11475532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236121-G-A

http://identifiers.org/hco/11/GRCh38#11475611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111236199-C-A

11475611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236199-C-T

http://identifiers.org/hco/11/GRCh38#11475659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111236221-C-A

11475690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236247-T-C

11475951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236971-G-T

11475956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111236976-G-A

http://identifiers.org/hco/11/GRCh38#11475969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111236989-C-A

http://identifiers.org/hco/11/GRCh38#11476039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111237066-C-A

11476076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111237103-T-C

11476287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111237325-T-C

11477042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238079-G-A

11477066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238103-A-G

11477188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238207-A-G

http://identifiers.org/hco/11/GRCh38#11477234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111238239-C-A

11477238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238243-C-T

11477240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238245-C-T

11477247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238252-G-A

11477247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238252-G-C

11477247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238252-G-T

11477302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238310-C-T

11477318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238326-G-A

http://identifiers.org/hco/11/GRCh38#11477390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111238396-C-A

11477762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238876-A-G

11477839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111238952-G-C

11478177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111239301-G-A

11478863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111239987-G-A

11478863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111239987-G-T

11478974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111240075-C-G

11479013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111240097-G-A

11479167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111240246-C-T

11479249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111240325-A-T

11479275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111240351-T-C

http://identifiers.org/hco/11/GRCh38#11479415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111240489-C-A

11479727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111240779-G-A

http://identifiers.org/hco/11/GRCh38#11479762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111240814-C-A

11481376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241048-G-T

http://identifiers.org/hco/11/GRCh38#11481418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111241093-A-C

11481429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241104-C-T

11481555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241228-T-C

11481694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241363-G-A

11481694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241363-G-T

11481710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241379-G-C

11481711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241380-T-C

11481732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241401-G-T

http://identifiers.org/hco/11/GRCh38#11482092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111241675-C-A

http://identifiers.org/hco/11/GRCh38#11482163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111241735-C-A

11482193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241765-G-C

11482232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241813-G-A

11482323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241890-G-A

11482363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241926-C-T

11482391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241954-G-T

11482419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111241983-G-A

11482576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111242079-T-G

11482847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111242348-G-A

11483030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111242647-T-C

http://identifiers.org/hco/11/GRCh38#11483225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111242814-C-A

http://identifiers.org/hco/11/GRCh38#11483309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111242869-C-A

11483359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111242915-A-T

11483401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111242942-T-C

11483704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111243213-C-T

11483761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111243270-G-A

11483826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111243300-A-G

http://identifiers.org/hco/11/GRCh38#11483835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111243309-A-C

11483909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111243383-G-C

11484039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111243508-G-A

11484186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111243655-C-T

11484650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111243803-G-T

11484711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111243860-G-C

11484747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111243890-C-T

http://identifiers.org/hco/11/GRCh38#11485592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111246466-C-A

11485882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246705-G-C

http://identifiers.org/hco/11/GRCh38#11485955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111246755-C-A

11486039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246818-C-G

http://identifiers.org/hco/11/GRCh38#11486057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111246836-C-A

11486084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246862-T-C

11486161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246905-C-T

11486201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246944-C-G

11486224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246968-G-A

11486243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246987-C-G

11486243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111246987-C-T

11486440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111247319-T-C

http://identifiers.org/hco/11/GRCh38#11486599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111247480-C-A

11486617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111247498-C-T

11486669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111247548-T-C

11486832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111247709-C-G

11486836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111247714-T-C

11487040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111247894-A-T

11487476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111249474-G-A

11487517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111249511-G-C

11487665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111249648-A-G

11487785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111249750-G-A

11487946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111249929-T-C

11488598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111250653-A-G

11488805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111250861-G-A

http://identifiers.org/hco/11/GRCh38#11488877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111250933-C-A

11488877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111250933-C-G

11488877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111250933-C-T

11488919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111250975-C-T

11489300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111251351-G-T

11489583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111251587-G-C

11489676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111251684-T-C

11489793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111251771-G-A

11489823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111251801-G-A

11489823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111251801-G-T

11490271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111252526-T-A

11490271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111252526-T-C

11490430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111252681-A-G

http://identifiers.org/hco/11/GRCh38#11490528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111252801-C-A

11490528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111252801-C-T

11490576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111252855-G-A

11490594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111252874-G-A

11490803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253044-T-C

11491084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253187-C-G

11491164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253258-T-G

http://identifiers.org/hco/11/GRCh38#11491223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111253341-A-C

11491247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253360-T-C

11491253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253366-A-T

11491260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253373-A-G

11491309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253418-A-G

11491327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253436-A-G

http://identifiers.org/hco/11/GRCh38#11491430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111253539-C-A

11491659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253755-T-C

11491684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111253780-C-T

http://identifiers.org/hco/11/GRCh38#11491862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111253925-A-C

11492273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111254331-G-A

11492441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111254489-T-A

11492448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111254496-T-C

http://identifiers.org/hco/11/GRCh38#11493566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111255116-A-C

11494288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111255523-T-C

11494459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111255678-C-T

http://identifiers.org/hco/11/GRCh38#11494546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111255764-C-A

http://identifiers.org/hco/11/GRCh38#11494614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111255820-C-A

11494662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111255866-T-C

11495078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111256283-C-T

11495188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111256392-G-A

11495888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111256499-T-C

11495985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111256577-T-A

11496117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111256702-G-T

11496252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111257051-T-C

11496261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111257060-C-T

11496316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111257119-A-G

11496416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111257211-C-T

11496605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111257360-G-A

11496738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111257481-C-T

11498229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111258181-A-G

11498563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111258374-C-G

http://identifiers.org/hco/11/GRCh38#11499391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111258918-C-A

11499401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111258928-T-A

11499747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111259255-C-T

11500184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111259678-G-T

11500207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111259702-G-A

11500507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111260762-G-A

11500723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111260953-C-T

http://identifiers.org/hco/11/GRCh38#11501095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111261743-C-A

11501095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111261743-C-T

11501165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111261808-G-A

11501174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111261817-C-T

11501452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111262089-T-C

11501925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111262479-G-T

11502252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111262803-G-A

11502319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111262877-C-T

11502350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111262908-G-A

11502804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111263384-T-C

11502896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111263463-T-C

11502962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111263502-G-C

11503581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111264561-T-A

11503778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111264810-G-T

http://identifiers.org/hco/11/GRCh38#11503808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111264845-A-C

11503827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111264864-G-A

11503920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111264943-A-T

11504099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265115-C-T

11504170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265188-G-A

11504170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265188-G-C

11504173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265191-C-T

11504354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265336-G-A

11504371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265352-T-C

11504372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265353-G-C

11504404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265385-G-A

11504865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265526-T-C

11505285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265834-T-C

11505388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265940-G-A

11505424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265978-C-T

http://identifiers.org/hco/11/GRCh38#11505429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111265983-C-A

11505430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111265984-A-G

11505891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111266406-T-G

11506575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267113-T-C

11506622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267160-A-G

11506638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267176-C-T

11506846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267372-G-A

11506893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267406-C-T

11506996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267487-C-T

11507139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267625-C-T

11507146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267632-T-A

11507154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267640-T-C

11507366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111267871-T-C

11507489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111268112-T-A

11508506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111271596-T-C

11508598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111271695-C-T

11508641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111271733-C-T

11508691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111271781-A-G

11508730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111271809-T-G

11508888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111271967-T-C

11509042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272086-G-A

11509094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272137-G-T

11509125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272172-T-C

11509126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272173-G-A

11509578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111272671-G-A

http://identifiers.org/hco/11/GRCh38#11509664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111272750-C-A

11510040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111273518-C-T

http://identifiers.org/hco/11/GRCh38#11510115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111273572-C-A

11510115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111273572-C-G

11510164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111273616-C-G

11510164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111273616-C-T

11510333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111273788-G-A

11510650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111274032-T-G

11510654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111274036-G-T

http://identifiers.org/hco/11/GRCh38#11510751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111274127-C-A

11510847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111274224-C-G

11510847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111274224-C-T

11511110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111274448-G-T

11511269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111274597-C-T

11511789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111275416-G-C

11511970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111275606-T-A

11511970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111275606-T-C

11512067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111275682-T-G

11512101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111275722-C-T

11512621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276441-C-T

11512654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276474-G-A

11512730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276552-T-A

11512730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276552-T-G

11512751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276573-G-C

11512959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111276770-C-T

11513231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277024-T-C

11513310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277101-C-T

11513336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277127-T-C

11513384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277176-T-A

11513712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277481-C-T

11513713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277482-G-A

11513713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277482-G-T

11513972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277729-C-T

11513989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277744-C-T

http://identifiers.org/hco/11/GRCh38#11513993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111277748-A-C

11513993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277748-A-G

11514014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277769-G-A

11514015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277770-A-T

11514081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111277832-G-C

http://identifiers.org/hco/11/GRCh38#11514278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111278024-C-A

11514606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111278845-T-A

11514785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279002-G-A

11514792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279009-C-T

11514885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279098-C-T

11514895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111279107-T-C

11516820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282324-G-A

11516859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282363-C-G

11516955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282455-T-C

11516965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282465-T-G

11516996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282496-C-T

11517532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111282998-G-A

11517959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283327-C-G

11517959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283327-C-T

11518116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283474-G-A

11518172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283524-T-C

11518327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111283674-A-G

11519237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284779-T-A

11519274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284813-G-A

11519291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284831-C-T

http://identifiers.org/hco/11/GRCh38#11519292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111284832-A-C

http://identifiers.org/hco/11/GRCh38#11519293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111284833-C-A

11519293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284833-C-T

11519439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111284968-C-T

11519685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285204-C-G

11519720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285236-G-A

11519767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285285-G-A

11519884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285378-C-T

11519990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285476-G-A

11520046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285534-T-C

http://identifiers.org/hco/11/GRCh38#11520061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111285548-C-A

11520064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285551-C-T

11520065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285552-C-T

11520125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285596-T-C

http://identifiers.org/hco/11/GRCh38#11520418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111285841-A-C

11520448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285864-A-G

11520523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285942-C-G

11520612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111285997-G-A

11520862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286299-A-G

11520952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286358-C-G

11520952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286358-C-T

11521052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286450-T-A

11521118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286514-C-T

11521254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286672-A-T

11523965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286934-C-T

11524024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111286989-C-T

11524090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287023-G-C

http://identifiers.org/hco/11/GRCh38#11524123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111287038-C-A

11524126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287041-T-C

11524140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287055-C-T

http://identifiers.org/hco/11/GRCh38#11524246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111287153-A-C

11524398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287309-C-G

11524424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287334-T-C

11524513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287421-G-A

11524632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287534-G-C

11524653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287555-C-G

11524815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287690-A-G

11524815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287690-A-T

http://identifiers.org/hco/11/GRCh38#11525051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111287936-A-C

11525052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111287937-G-A

11525147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288068-T-C

11525171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288091-A-G

11525171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288091-A-T

11525218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288138-G-A

11525218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288138-G-T

11525237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288159-C-T

11525356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288283-A-G

11526157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288755-A-T

11526452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111288942-C-T

11526510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289004-T-C

11527015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289221-G-A

11527122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289335-C-T

11527163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289376-C-T

11527593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289767-T-G

http://identifiers.org/hco/11/GRCh38#11527602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111289770-C-A

11527614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289782-A-G

11527837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111289977-A-G

11527996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290120-T-A

11527996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290120-T-C

11528062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290171-G-C

11528110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290217-A-G

11528249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290337-T-C

http://identifiers.org/hco/11/GRCh38#11528315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111290402-A-C

11528655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290700-A-T

11532524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111290945-T-C

11532843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291255-G-A

11533089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291522-C-T

http://identifiers.org/hco/11/GRCh38#11533282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111291766-C-A

11533425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291899-G-A

11533504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291989-G-A

11533521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291993-C-G

11533521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111291993-C-T

11533562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292012-G-A

11534030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292394-A-G

11534030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292394-A-T

11534043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292406-C-T

11534080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292423-T-A

11534096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292439-C-T

11534099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292442-G-C

11534488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292819-A-G

11534515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292841-T-C

11534557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292882-A-G

11534571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292889-T-A

11534768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111292985-G-C

11534902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293106-C-T

11534934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293124-C-T

11534953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293137-C-T

11534958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293142-G-A

11535010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293197-G-C

11535036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293223-C-T

11535081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293265-T-A

11535081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293265-T-C

11535127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293312-A-G

11535140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293325-C-T

11535529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293626-G-T

11535630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293716-T-C

11535667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111293734-G-A

11536046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294122-T-C

11536065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294141-T-C

11536113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294192-G-C

11536158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111294236-A-T

11536663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111295530-A-T

11537385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111296451-A-G

11537505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111296560-T-C

11537505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111296560-T-G

http://identifiers.org/hco/11/GRCh38#11537585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111296634-C-A

11537665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111296684-C-T

11537762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111296778-A-G

http://identifiers.org/hco/11/GRCh38#11537765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111296785-A-C

11537833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111296851-T-A

11538036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297035-C-T

http://identifiers.org/hco/11/GRCh38#11538140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111297124-C-A

11538207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297537-A-G

11538301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297631-G-T

11538481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111297794-G-A

http://identifiers.org/hco/11/GRCh38#11539517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111298062-C-A

11539517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298062-C-T

11540101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298635-C-T

http://identifiers.org/hco/11/GRCh38#11540115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111298650-A-C

11540122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298657-T-C

11540264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111298797-G-A

11543205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299662-T-C

11543331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299816-T-C

11543498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299977-G-A

11543521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111299998-C-T

11544826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301260-C-T

11545265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301651-A-T

11545366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301736-G-C

11545367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301737-G-A

11545487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301852-A-G

11545625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111301992-C-T

11545653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302027-C-T

11545671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302045-C-T

http://identifiers.org/hco/11/GRCh38#11545735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111302096-C-A

11545735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302096-C-T

http://identifiers.org/hco/11/GRCh38#11545804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111302156-A-C

11545837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302189-C-G

11546221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302448-G-A

11546297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302518-C-T

11546488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302698-A-T

11546576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302786-A-G

11546714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302914-C-G

11546726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111302924-C-T

http://identifiers.org/hco/11/GRCh38#11546778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111302974-C-A

11546845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303044-G-A

11546933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303142-T-C

11546961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303203-T-C

11547048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303288-T-C

11547048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303288-T-G

11547105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303339-A-G

11547509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111303715-G-A

http://identifiers.org/hco/11/GRCh38#11548008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111303975-C-A

11548086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304034-T-C

11548279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304222-G-T

11548332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304269-T-C

11548349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304286-G-A

11548352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304289-G-A

11548352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304289-G-T

11548480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304421-G-A

http://identifiers.org/hco/11/GRCh38#11548629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111304598-C-A

11548635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304604-T-C

11548662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304631-C-T

http://identifiers.org/hco/11/GRCh38#11548791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111304760-A-C

11548791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111304760-A-G

11549064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305744-G-C

11549211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305894-G-A

11549275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111305959-G-T

11549472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306098-A-G

11549481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306107-C-G

11549481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306107-C-T

11549660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306238-C-T

11549781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111306375-G-T

11551189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307801-G-A

http://identifiers.org/hco/11/GRCh38#11551283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111307904-C-A

11551283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307904-C-T

11551284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111307905-T-G

11553739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309535-C-T

11553976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309758-A-G

11554085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309856-C-T

11554094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309866-C-G

11554094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309866-C-T

http://identifiers.org/hco/11/GRCh38#11554169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111309921-C-A

11554265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310019-C-G

11554297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310048-C-T

11554339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310090-G-A

11554397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310128-C-T

11554430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310148-G-A

11554517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310239-G-A

11554963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310815-G-A

11555129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310975-C-T

11555141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310987-T-C

11555479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111311295-C-G

11555554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313094-A-T

http://identifiers.org/hco/11/GRCh38#11555607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111313155-A-C

http://identifiers.org/hco/11/GRCh38#11555616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111313168-C-A

11555616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313168-C-T

11555832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313363-C-T

11555873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313399-C-T

11556066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313594-G-A

11556081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313602-G-A

http://identifiers.org/hco/11/GRCh38#11556102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111313615-C-A

11556275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313777-G-T

11556474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314085-C-T

11556496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314107-G-A

11556496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314107-G-C

11556755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314392-G-C

11556755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314392-G-T

11556781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314417-G-T

11556979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314598-C-T

11557182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314792-G-A

11557199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314810-A-T

11557280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111314901-T-G

11557436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315005-C-T

11557615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315110-C-T

11557907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315405-G-A

11557942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315458-T-C

http://identifiers.org/hco/11/GRCh38#11557949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111315465-C-A

11557949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315465-C-T

11558143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315619-G-A

11558198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315674-G-A

11558206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315682-T-C

11558316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315801-A-G

11558465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111315943-G-T

11558649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316107-T-C

11558851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316268-T-C

11559082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316429-T-C

11559110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316457-T-C

11559119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316466-T-C

11559120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111316467-T-C

11560467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317041-C-T

11560704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317259-C-T

http://identifiers.org/hco/11/GRCh38#11560882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111317365-A-C

11560882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317365-A-G

11560951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317436-G-A

11561147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317631-T-A

11561175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317657-G-C

11561230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317712-C-T

11561266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317751-G-A

11561457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111317951-T-C

http://identifiers.org/hco/11/GRCh38#11561513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111318004-A-C

11561864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318346-A-G

11561872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318354-C-T

11561899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318381-C-G

11561899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318381-C-T

11562168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318889-G-A

11562238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318976-T-A

11562238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111318976-T-C

11562314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319045-T-C

11562328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319055-T-G

11562446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319141-T-C

11562456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319151-G-A

11562471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319166-G-T

http://identifiers.org/hco/11/GRCh38#11562598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111319300-C-A

11562602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319304-A-G

11562612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319315-T-C

http://identifiers.org/hco/11/GRCh38#11562622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111319327-C-A

11562632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319353-G-A

11562632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319353-G-T

11562773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319482-C-T

11563007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319667-T-C

http://identifiers.org/hco/11/GRCh38#11563079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111319698-A-C

11563364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111319897-G-A

11563585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320091-A-G

11563632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320136-T-A

11563697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320203-C-T

11563960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320484-T-C

11564052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320571-G-T

11564212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320729-C-G

11564212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320729-C-T

11564213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320730-G-A

11564382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111320866-G-A

11564677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321132-C-T

11564727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321161-T-C

11564781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321216-C-T

11564858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321290-T-C

11564878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321310-C-T

11565012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321452-G-A

http://identifiers.org/hco/11/GRCh38#11565192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111321592-C-A

11565198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321598-G-A

11565198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321598-G-T

11565363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321751-C-T

11565405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321791-G-A

11565481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321862-G-A

11565482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321863-C-T

11565489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321870-G-A

11565489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321870-G-C

11565514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321895-G-A

11565594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111321975-T-C

11565990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111322290-G-A

11566034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111322334-G-A

11566100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111322412-T-C

http://identifiers.org/hco/11/GRCh38#11566279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111322584-C-A

11566314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111322619-T-C

11566466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111322985-G-A

11566878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323393-G-A

11566883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323398-T-C

11566957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323469-G-A

11567240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323711-G-T

11567261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323732-A-G

11567432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323905-T-G

11567513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111323985-T-C

11567703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111324186-G-A

11567846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111324282-T-C

11568259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111324683-T-G

http://identifiers.org/hco/11/GRCh38#11568411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111324821-C-A

11568668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111325033-G-A

http://identifiers.org/hco/11/GRCh38#11568942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111325306-A-C

11569235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111325554-G-A

11569829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326273-T-A

11569895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326334-C-T

11569948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326387-G-A

11569984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326423-A-G

11569994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326447-G-T

http://identifiers.org/hco/11/GRCh38#11570046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111326500-C-A

11570046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326500-C-T

http://identifiers.org/hco/11/GRCh38#11570143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111326578-C-A

11570143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326578-C-G

11570143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326578-C-T

11570188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326609-A-G

11570188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111326609-A-T

11570204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111326623-C-G

11570204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111326623-C-T

11570209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326628-T-C

11570209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326628-T-G

http://identifiers.org/hco/11/GRCh38#11570309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111326720-C-A

11570309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326720-C-G

11570384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326794-G-A

11570401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326812-C-T

11570423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111326826-C-T

11571370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111329504-T-A

11571543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111329687-A-G

11571543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111329687-A-T

11571574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111329714-G-A

11571693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111329824-A-G

11571785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111329914-T-C

11571928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330061-C-T

11571939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330071-A-G

11572119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330222-G-A

11572142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330245-C-T

11572233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330325-A-T

11572665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330723-A-T

11572680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330738-A-G

11572731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111330791-C-T

http://identifiers.org/hco/11/GRCh38#11572819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111330873-C-A

11574634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331351-T-A

11574634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331351-T-G

11574854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331574-T-C

11574860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331580-G-A

11574887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331607-T-C

11574894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331614-C-T

11575147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331833-T-C

11575160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331846-G-A

http://identifiers.org/hco/11/GRCh38#11575241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111331906-C-A

11575241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111331906-C-T

11575445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111332106-G-C

11576044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111333062-G-C

11578000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111334173-C-T

11578056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111334226-G-A

11578056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111334226-G-T

11578125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111334292-G-A

11578252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111334414-G-A

11578461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111334580-T-C

http://identifiers.org/hco/11/GRCh38#11578476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111334595-A-C

11578506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111335140-G-C

11579122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111335737-T-A

11579634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111336891-G-A

11579958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337221-G-A

11579966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337227-A-G

11580032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337296-A-G

http://identifiers.org/hco/11/GRCh38#11580231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111337584-C-A

11580367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337685-G-T

11580428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337725-G-A

11580510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337802-G-A

11580515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337807-T-A

11580586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337877-C-T

11580657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111337946-T-A

11580908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338160-G-A

11580926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338177-C-T

11580977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338227-G-A

11580977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338227-G-C

11581105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338346-G-C

11581318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338570-A-T

11581358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338611-G-C

http://identifiers.org/hco/11/GRCh38#11581472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111338728-C-A

11581511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338768-C-T

11581655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111338931-G-A

11581735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339001-A-G

11581747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339013-T-A

11581747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339013-T-C

11581747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339013-T-G

11581830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339067-C-T

11581915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339153-C-G

11581947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339174-G-A

11582049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339263-A-T

11582162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339335-G-C

11582299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339443-C-T

http://identifiers.org/hco/11/GRCh38#11582338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111339495-C-A

11582338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339495-C-T

11582428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339589-A-T

11583149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339845-T-A

http://identifiers.org/hco/11/GRCh38#11583165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111339857-C-A

11583203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339885-A-G

11583338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111339961-T-C

11583601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340228-C-T

11583643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340373-C-T

11583674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340404-A-T

11583714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340449-T-C

11583865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340595-A-G

11583916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340649-G-A

11583932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340665-C-G

11583932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340665-C-T

11584018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111340727-G-C

11584508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111341153-G-A

11584527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111341172-G-A

http://identifiers.org/hco/11/GRCh38#11584534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111341178-C-A

11584534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111341178-C-T

11584583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111341226-T-C

11584716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111341351-G-A

11584913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111341535-A-G

11584976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111341601-G-A

11585638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111342198-G-A

11585737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111342272-T-C

11586287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111342738-A-G

11587723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111343757-C-G

11587739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111343772-T-C

11587907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111343926-C-G

http://identifiers.org/hco/11/GRCh38#11588035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111344035-C-A

11588121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111344131-C-T

11588482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111344580-C-T

11588575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111344659-C-G

11588576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111344660-T-A

11588715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111344812-T-C

11588734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111344831-A-G

11588921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345504-T-C

11589048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345627-C-G

11589076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345654-T-C

11589076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345654-T-G

11589105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345680-T-G

11589153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345728-C-T

11589394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111345904-T-C

http://identifiers.org/hco/11/GRCh38#11589469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111346002-A-C

11589588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111346337-T-G

11589932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111346665-G-A

11591618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348121-T-G

11591698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348210-A-G

11591709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348221-T-G

11591736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348248-C-T

11591845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348343-G-A

11592175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348676-A-G

11592213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348714-G-A

11592361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348862-G-A

11592513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111348999-T-C

11592622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349105-C-G

11592669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349153-C-T

11592757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349243-C-T

11592799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349279-G-A

11592955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349434-T-G

11593256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349619-G-A

11593332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349673-G-A

11593450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111349786-T-C

11593869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350171-C-T

11593954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350238-T-C

http://identifiers.org/hco/11/GRCh38#11594216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111350490-C-A

11594216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350490-C-T

11594255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350529-C-G

11594372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350634-G-A

11594385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350650-G-A

11594385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350650-G-T

11594393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350659-C-T

11594512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350763-A-G

11594521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350776-T-C

11594706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111350955-T-C

http://identifiers.org/hco/11/GRCh38#11601079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111355146-C-A

11601540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111355559-T-A

11601561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111355579-T-A

11602188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111356001-A-G

11602476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111356278-T-G

11603060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111357057-C-T

11603104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111357138-G-C

11603121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111357155-A-G

11603121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111357155-A-T

http://identifiers.org/hco/11/GRCh38#11603239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111357277-A-C

11603412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358011-A-G

11603412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358011-A-T

11603622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358216-A-T

11603812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358386-G-C

11603812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358386-G-T

11604039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358545-T-C

11604099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111358604-C-T

11604397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359110-G-T

http://identifiers.org/hco/11/GRCh38#11604547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111359235-C-A

11604547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359235-C-T

11604576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359273-A-G

11604583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359280-G-T

http://identifiers.org/hco/11/GRCh38#11604713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111359427-A-C

11604758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359471-A-G

11604788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359501-T-C

11604788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359501-T-G

11604853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359566-G-C

11604853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359566-G-T

11604904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359617-G-A

11604952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359686-A-G

11605127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359857-C-T

11605145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359875-G-A

11605157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111359895-C-T

http://identifiers.org/hco/11/GRCh38#11605214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111359950-C-A

11605262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111360010-G-T

11605373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111360111-C-T

11605594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111361835-C-G

http://identifiers.org/hco/11/GRCh38#11605911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111362153-C-A

11605911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111362153-C-T

http://identifiers.org/hco/11/GRCh38#11606469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111363031-C-A

11606875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111363457-G-T

http://identifiers.org/hco/11/GRCh38#11606897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111363478-A-C

11607840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111364348-T-C

11607840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111364348-T-G

11608149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111364601-G-A

11608174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111364626-T-G

11608692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365245-G-T

11608797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365348-C-T

http://identifiers.org/hco/11/GRCh38#11608801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111365349-C-A

11608842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111365386-A-T

11609034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365450-C-T

11609091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111365506-T-C

11609135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365560-G-A

http://identifiers.org/hco/11/GRCh38#11609173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111365600-C-A

11609173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365600-C-T

11609276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365680-C-T

http://identifiers.org/hco/11/GRCh38#11609301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111365703-C-A

11609392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365797-C-T

11609407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365812-A-T

11609410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365815-T-C

11609465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365872-A-G

11609512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365917-C-T

11609555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111365964-A-G

11609600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366009-G-A

11609638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366047-T-C

http://identifiers.org/hco/11/GRCh38#11609721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111366128-C-A

11610003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366384-A-G

11610107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366473-G-C

11610309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366672-T-C

11610325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366687-C-G

11610366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366728-A-G

11610505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366873-T-A

11610505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366873-T-C

11610580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111366940-T-C

11610669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111367320-A-G

11610669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111367320-A-T

11611040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111367748-G-A

11611040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111367748-G-C

11611100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111367803-G-A

11611311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368013-C-T

11611312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368014-T-C

11611362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368047-G-T

11611369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368054-G-A

http://identifiers.org/hco/11/GRCh38#11611371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111368056-C-A

11611371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368056-C-G

11611372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368057-A-T

11611543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368200-A-G

11611745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368271-C-G

11611862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368356-T-C

11611867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368361-G-A

11611960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368447-G-C

11612067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368550-G-A

11612098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111368580-C-T

11612169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111369098-C-G

11612313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111369212-T-C

11612503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111369852-C-T

11612516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111369865-A-G

11612572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111369922-A-G

11612874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370165-A-G

11612959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370249-G-T

11613071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370361-T-C

11613082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370372-G-A

11613105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370392-A-G

http://identifiers.org/hco/11/GRCh38#11613174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111370461-A-C

11613208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370487-T-C

11613209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111370488-C-T