27870010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66002152-G-T

27870222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001962-T-G

27870225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001941-T-G

27870234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001932-T-C

27870235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001931-T-A

27870436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001745-G-A

27870436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001745-G-T

27870437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001744-G-A

http://identifiers.org/hco/8/GRCh38#27870476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66001704-C-A

27870476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001704-C-T

http://identifiers.org/hco/8/GRCh38#27870504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66001672-C-A

27870504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001672-C-T

http://identifiers.org/hco/8/GRCh38#27870523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66001653-A-C

27870718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001474-A-G

http://identifiers.org/hco/8/GRCh38#27870725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66001467-C-A

27870725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001467-C-T

http://identifiers.org/hco/8/GRCh38#27870965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66001269-C-A

27871000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001244-G-A

27871000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001244-G-T

27871107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001129-A-G

27871125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001112-A-G

27871125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001112-A-T

27871214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001015-T-A

27871214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66001015-T-C

http://identifiers.org/hco/8/GRCh38#27871319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66000918-C-A

27871382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000860-G-A

27871382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000860-G-T

27871385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000857-T-A

27871385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000857-T-C

http://identifiers.org/hco/8/GRCh38#27871399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66000845-A-C

http://identifiers.org/hco/8/GRCh38#27871447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66000799-A-C

27871447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000799-A-G

27871543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000712-T-C

27871584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000666-T-A

27871584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000666-T-G

http://identifiers.org/hco/8/GRCh38#27871589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66000661-A-C

27871589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000661-A-G

http://identifiers.org/hco/8/GRCh38#27871613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66000637-C-A

27871660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000588-G-A

27871660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000588-G-C

27871724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000523-G-A

27871724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000523-G-T

http://identifiers.org/hco/8/GRCh38#27871779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#66000469-C-A

27871779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000469-C-T

27871828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000411-C-G

27871828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000411-C-T

27871871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000373-C-G

27871871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3 prime UTR variant
orthologous variants: 66000373-C-T

27872384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65999969-C-T

http://identifiers.org/hco/8/GRCh38#27872811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65999560-A-C

27872948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65999423-C-G

27872974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65999382-C-T

27878131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65997747-C-G

27878365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65997501-T-C

27878394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65997468-G-T

27879490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65997314-G-T

27879507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65997297-T-A

http://identifiers.org/hco/8/GRCh38#27879783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65997016-C-A

http://identifiers.org/hco/8/GRCh38#27879792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65997007-C-A

http://identifiers.org/hco/8/GRCh38#27879816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65996984-C-A

27879816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996984-C-G

27884290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65996610-G-A

27884400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996511-G-A

27884415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996508-C-T

27884418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996505-G-T

27884566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996355-G-A

27884616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996306-A-G

27884686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65996231-C-G

27884711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996172-C-T

27884734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996153-G-A

27884746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65996138-C-T

http://identifiers.org/hco/8/GRCh38#27884940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65995925-C-A

27885089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995781-G-T

27885219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995658-A-G

27885298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995585-G-A

27885298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995585-G-C

27885336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995554-G-C

27885554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995355-G-T

27885717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995221-G-A

27885884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995051-T-G

27885900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995035-G-T

27885902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65995033-A-G

http://identifiers.org/hco/8/GRCh38#27886011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65994935-C-A

27886011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994935-C-G

27886011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994935-C-T

27886150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994809-C-T

27886153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994806-C-T

http://identifiers.org/hco/8/GRCh38#27886154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65994805-A-C

27886234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994754-T-A

27886234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994754-T-C

http://identifiers.org/hco/8/GRCh38#27886252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65994736-C-A

27886252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994736-C-T

27886276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994712-T-C

27886383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994606-T-C

27886473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994521-G-A

27886576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994417-A-G

27886686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65994305-G-A

27886834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993749-C-T

27888724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993262-A-G

27888784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993216-C-T

27888892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993129-G-A

27888903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993118-T-C

27888980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993041-A-T

27889003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993022-C-G

27889023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65993002-C-T

27889032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992994-C-T

27889044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992982-C-T

27889218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992834-G-T

27889335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992754-C-T

27889484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992624-G-A

27889660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992526-A-G

27889760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992436-G-T

27890175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992112-C-T

27890248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992041-C-G

27890248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65992041-C-T

27890357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65991950-A-G

27890402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65991887-A-G

27890914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65991679-T-G

27890944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65991629-C-G

27890966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65991611-C-T

27891088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65991502-G-A

http://identifiers.org/hco/8/GRCh38#27891116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65991478-A-C

27891138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65991463-C-T

27892117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990843-A-T

27892153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990795-G-A

27892258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990699-A-G

27892448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990529-G-T

27893086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990312-C-T

27893105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990292-T-C

27893116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990281-G-A

http://identifiers.org/hco/8/GRCh38#27893117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65990280-C-A

27893124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990273-G-T

27893192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990216-T-A

27893237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990178-G-A

27893237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990178-G-C

27893240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990164-A-T

27893269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990133-G-A

27893269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990133-G-C

27893270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65990132-T-C

27893497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989922-G-A

27893872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989554-C-T

27893873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989553-C-T

27894097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989331-G-C

27894113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989321-G-C

27894200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989233-T-C

27894401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65989051-G-A

27894552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65988890-G-A

27894563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65988879-T-G

http://identifiers.org/hco/8/GRCh38#27894635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65988817-A-C

27894635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65988817-A-G

27894716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65988754-C-T

27894773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65988691-C-G

27894937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987931-C-G

27894937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987931-C-T

http://identifiers.org/hco/8/GRCh38#27894988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65987879-A-C

27895208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987661-G-C

27895216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987641-G-A

27895419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987439-A-T

27895502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987375-G-A

27895537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987341-A-G

27895622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987295-G-A

27895697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65987218-G-A

27897116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65985327-T-C

27897116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65985327-T-G

27897326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65985152-G-A

27897326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65985152-G-C

27897343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65985135-G-T

27897613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65984627-G-A

27897648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65984591-T-C

27897730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65984544-T-G

27897782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65984491-A-G

27900794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65982324-T-G

27900821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65982297-C-G

27900821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65982297-C-T

http://identifiers.org/hco/8/GRCh38#27900833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65982273-C-A

27900878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65982220-T-G

27901026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65982086-G-A

27901047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65982064-A-G

27901200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65981929-A-G

27901351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65981781-G-A

27901351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65981781-G-T

http://identifiers.org/hco/8/GRCh38#27901359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65981772-C-A

27901649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65981519-G-C

27901690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65981472-A-G

27901928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65981271-C-T

27902020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65981178-T-C

27902676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65980616-G-A

27904025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980271-T-A

http://identifiers.org/hco/8/GRCh38#27904236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65980082-C-A

http://identifiers.org/hco/8/GRCh38#27904278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65980047-A-C

27904278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980047-A-G

27904278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980047-A-T

http://identifiers.org/hco/8/GRCh38#27904292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65980033-A-C

27904292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980033-A-G

27904305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980017-G-A

27904305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980017-G-C

27904305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980017-G-T

http://identifiers.org/hco/8/GRCh38#27904311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65980010-A-C

27904311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65980010-A-G

27904333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979988-T-C

http://identifiers.org/hco/8/GRCh38#27904555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65979800-C-A

27904555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65979800-C-G

27904555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65979800-C-T

27904620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65979760-T-G

27904690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65979689-T-A

27904790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 65979623-C-T

27904854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979560-T-C

http://identifiers.org/hco/8/GRCh38#27904899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65979518-C-A

27904899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979518-C-T

http://identifiers.org/hco/8/GRCh38#27904942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65979475-C-A

27904945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979472-G-A

http://identifiers.org/hco/8/GRCh38#27904949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65979468-C-A

http://identifiers.org/hco/8/GRCh38#27905004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65979425-C-A

27905109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979329-G-T

27905401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979086-G-A

http://identifiers.org/hco/8/GRCh38#27905420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65979040-C-A

27905420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979040-C-T

27905429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65979031-G-A

http://identifiers.org/hco/8/GRCh38#27905549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65978922-C-A

27905549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65978922-C-T

http://identifiers.org/hco/8/GRCh38#27905566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65978907-A-C

27905575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65978898-G-A

http://identifiers.org/hco/8/GRCh38#27905695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65978797-C-A

27905695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65978797-C-T

27905898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65978781-A-G

27906164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65978636-A-G

27906446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65978131-C-T

27907105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977883-G-C

27907105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977883-G-T

http://identifiers.org/hco/8/GRCh38#27907121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65977863-C-A

27907121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977863-C-T

27907174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 65977809-C-T

27907194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 65977789-A-G

27907205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 65977778-T-C

27907249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 65977734-G-C

27907249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 65977734-G-T

http://identifiers.org/hco/8/GRCh38#27907259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65977724-C-A

27907259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977724-C-T

27907313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977680-G-A

27907313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977680-G-T

27907442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977582-T-C

27907995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65977209-A-G

http://identifiers.org/hco/8/GRCh38#27908322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65977009-C-A

27908422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976914-A-G

27908435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976903-T-A

27908652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976674-T-C

27908912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976446-G-C

27908968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976405-T-A

27908968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976405-T-C

27908968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976405-T-G

27909007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976368-G-A

http://identifiers.org/hco/8/GRCh38#27909073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65976313-C-A

27909390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976186-G-A

http://identifiers.org/hco/8/GRCh38#27909497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65976081-A-C

27909517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976061-T-C

27909520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976058-G-A

27909520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976058-G-T

27909528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976050-T-C

27909528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976050-T-G

27909547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976038-G-A

27909547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976038-G-T

27909596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976011-A-G

27909607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976000-G-A

27909607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976000-G-C

27909607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65976000-G-T

27909624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975988-G-A

27909624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975988-G-T

27909625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975987-G-A

27909625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975987-G-C

27909625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975987-G-T

27909630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975982-C-T

27909647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975966-G-A

27909647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975966-G-C

27909647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975966-G-T

http://identifiers.org/hco/8/GRCh38#27909750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975862-A-C

27909750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 65975862-A-G

27909892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975730-G-A

27909892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975730-G-T

27909900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975722-T-C

27909996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975653-C-T

27910020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975630-T-C

27910031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975619-T-C

27910049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975607-C-T

http://identifiers.org/hco/8/GRCh38#27910180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975270-A-C

27910180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 65975270-A-G

http://identifiers.org/hco/8/GRCh38#27910230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975218-C-A

27910230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975218-C-T

27910240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975208-G-A

27910240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975208-G-C

27910240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975208-G-T

http://identifiers.org/hco/8/GRCh38#27910247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975201-C-A

http://identifiers.org/hco/8/GRCh38#27910280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975167-C-A

27910280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975167-C-G

27910280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975167-C-T

27910303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975143-T-A

27910303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975143-T-C

27910303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65975143-T-G

27910317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975129-T-C

27910317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975129-T-G

http://identifiers.org/hco/8/GRCh38#27910340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975107-C-A

27910340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975107-C-T

27910347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975100-T-C

27910368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975080-C-G

27910368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975080-C-T

http://identifiers.org/hco/8/GRCh38#27910369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65975079-C-A

27910369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975079-C-T

27910400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975048-A-G

27910414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65975034-G-T

27910477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974971-G-A

27910546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974908-A-G

27910556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974898-C-T

27910686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974760-C-T

27910797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974653-C-T

27910962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974498-A-G

27911030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974431-A-G

27911045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974419-G-A

27911055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974409-G-C

27911145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974345-T-C

27911329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974247-T-G

27911372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974206-C-T

27911850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974103-T-G

27911857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65974096-G-A

27912033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65973971-C-T

27912065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65973941-T-G

27912175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65973847-C-T

27912528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65973480-C-G

27912528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65973480-C-T

27915222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972983-C-G

27915421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972793-C-T

http://identifiers.org/hco/8/GRCh38#27915445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65972776-C-A

27915555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972685-A-G

27915573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972668-G-T

27915633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972588-T-A

27915633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972588-T-G

27916156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65972122-A-G

27921337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968874-G-A

27921424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968786-G-T

27921425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968785-A-G

http://identifiers.org/hco/8/GRCh38#27921436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65968777-A-C

27921436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968777-A-G

27921497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968737-T-C

27921505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968719-G-A

27921505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968719-G-T

27921520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65968704-A-G

27921594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, missense_variant
orthologous variants: 65968619-A-G

27921698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968515-G-T

27921708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968505-C-T

http://identifiers.org/hco/8/GRCh38#27921734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65968479-C-A

27921734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968479-C-T

27921798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968415-A-G

27921812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968401-G-A

27921812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968401-G-T

http://identifiers.org/hco/8/GRCh38#27921876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65968337-C-A

27921876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968337-C-T

http://identifiers.org/hco/8/GRCh38#27921974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65968239-C-A

27921974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968239-C-T

http://identifiers.org/hco/8/GRCh38#27921987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65968226-A-C

27921987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968226-A-G

27922041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968172-A-G

27922055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968158-G-A

27922055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968158-G-T

http://identifiers.org/hco/8/GRCh38#27922067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65968146-C-A

27922067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 65968146-C-T

27922080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968133-G-A

27922080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 65968133-G-C

27922203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968010-G-A

27922203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 65968010-G-T

27922292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967927-G-A

27922292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967927-G-C

27922292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967927-G-T

27922391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967836-T-A

27922391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967836-T-C

27922391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967836-T-G

27922392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967835-T-A

27922392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967835-T-C

27922392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65967835-T-G

27922714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65966694-G-C

27922781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65966633-T-C

27922806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65966604-G-A

27922806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65966604-G-T

http://identifiers.org/hco/8/GRCh38#27922892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65966541-C-A

27922912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65966521-G-C

27923040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65966481-G-C

27926853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65964079-G-C

27926876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65964056-T-C

27927506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65963534-T-A

27927528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65963517-T-C

27927733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65963287-G-T

27927842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962895-T-C

27928443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962284-A-G

27928462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962265-T-C

27928563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962158-G-T

27928571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962150-G-A

27928578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962145-G-A

27928590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65962133-C-G

27929081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65961995-T-C

27929172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65961912-C-T

27929197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65961879-C-G

27929490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65961594-T-C

27929817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65960651-C-G

27930013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65960472-A-G

27930828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65960348-C-T

27931000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65960185-G-C

27933231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65958788-G-A

27933832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65957101-G-A

27933980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65956959-G-T

27934581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65956409-T-C

27934636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65956357-C-T

27934689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65956306-A-G

27934870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65956138-T-G

27934891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65956117-C-T

27936680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65955987-A-T

27937205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65955459-A-G

27937226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65955394-T-C

27937242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65955341-A-G

27937311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65955273-C-T

27938209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65953372-C-G

27938287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65953297-A-G

http://identifiers.org/hco/8/GRCh38#27938294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65953290-C-A

27938469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65953115-G-A

http://identifiers.org/hco/8/GRCh38#27938568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65953026-C-A

27938568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65953026-C-G

27938604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65952983-T-C

27938656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65952931-C-T

27939214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65950526-T-A

27939214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65950526-T-C

27939368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65950378-G-A

27939621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65950025-C-T

27939704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65949933-C-T

27939959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65949710-C-T

27940044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65949624-T-C

27940136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65949533-T-G

27940392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65949295-T-C

http://identifiers.org/hco/8/GRCh38#27940676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65948997-A-C

27941440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65948153-A-G

27941455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65948138-G-A

27941455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65948138-G-T

27941508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65948087-T-C

27942199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65947587-G-T

27942387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65947409-G-C

27942566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65946592-G-A

27942617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65946541-T-G

http://identifiers.org/hco/8/GRCh38#27942623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65946535-C-A

27942667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65946490-G-A

http://identifiers.org/hco/8/GRCh38#27942763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65946395-A-C

27942798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65946361-T-C

27943880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65945681-T-A

27944892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65944774-G-A

27945764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65944015-G-C

27946091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65943663-T-C

27946251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65943497-C-T

27948315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65941946-C-T

27948358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65941904-G-A

27948358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65941904-G-T

27948712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron_variant, undefined
orthologous variants: 65941564-C-T

27948875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65941405-A-G

27949181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65941130-G-A

27949181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65941130-G-T

27952752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65939301-T-C

27952862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65939249-C-T

27952895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65939216-A-G

http://identifiers.org/hco/8/GRCh38#27953290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65938840-C-A

27953766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65938430-T-C

27953961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65938004-A-G

27954186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65937852-A-G

27956739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935613-G-A

27956739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935613-G-C

27956739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935613-G-T

27956745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935607-C-T

27956765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935587-C-G

27956765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935587-C-T

27957065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935309-G-A

27957123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65935280-A-G

27957665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934948-A-G

27957724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934907-C-T

27957764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934869-T-C

27957920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934731-A-G

27957937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934713-A-G

27958127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934158-C-T

27958273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65934020-G-A

27958682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65933686-G-C

27958738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65933631-G-A

27958884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65933489-A-G

27959147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65933218-C-T

http://identifiers.org/hco/8/GRCh38#27959167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65933205-A-C

27959167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65933205-A-G

27960555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65932682-T-C

27960632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65932614-A-G

27960634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65932612-G-A

27960689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65932558-G-A

27961601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931896-T-C

27961702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931799-C-T

27961753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931753-A-G

27961766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931740-G-A

27961969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931520-C-T

27962112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931383-A-G

27962151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931345-T-C

http://identifiers.org/hco/8/GRCh38#27962275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65931227-C-A

27962275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931227-C-T

27962341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931159-G-A

27962341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931159-G-C

27962350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65931150-A-T

27962585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65930946-G-A

27962585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65930946-G-T

27962587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65930944-A-G

27962785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65930755-G-A

27964168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929894-C-T

http://identifiers.org/hco/8/GRCh38#27964196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65929853-C-A

27964199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929847-T-G

27964226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929820-C-T

27964272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929774-G-A

27964452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929600-A-G

27964500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929552-C-T

27964571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929481-T-G

27964589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929463-T-G

http://identifiers.org/hco/8/GRCh38#27964971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65929107-C-A

27965052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65929026-C-T

27965190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65928894-T-C

27965424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65928667-A-G

27965690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65928451-C-T

27965719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65928423-A-G

http://identifiers.org/hco/8/GRCh38#27966189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65927589-A-C

27966189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927589-A-G

27966237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927538-G-T

27966282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927494-T-C

27966283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927493-T-C

27966284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927492-C-T

http://identifiers.org/hco/8/GRCh38#27966288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65927468-C-A

27966288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927468-C-T

27966298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927458-G-T

27966352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927405-T-C

27966352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927405-T-G

27966540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 65927217-G-A

http://identifiers.org/hco/8/GRCh38#27966664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65927124-C-A

27966682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927106-T-C

http://identifiers.org/hco/8/GRCh38#27966684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65927104-C-A

27966684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927104-C-T

http://identifiers.org/hco/8/GRCh38#27966687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65927101-C-A

27966687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927101-C-T

27966693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927094-G-A

27966693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927094-G-C

27966693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65927094-G-T

27967335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65924540-G-A

27967395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65924481-G-T

27967455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65924415-T-A

27967455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65924415-T-G

27968388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65923300-T-A

27968606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65923104-T-G

27968622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65923088-G-C

27969074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65922653-T-C

http://identifiers.org/hco/8/GRCh38#27973521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65919705-C-A

27973532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919694-T-C

27973554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919672-C-G

27973824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919472-T-A

27973824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919472-T-C

27973824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919472-T-G

27973864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919443-C-T

27974271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919222-C-T

27974353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919137-G-A

27974375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919113-C-G

27974375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919113-C-T

27974421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65919073-T-C

27974519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65918979-C-T

27975031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65918453-G-C

27975031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65918453-G-T

27975444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65918042-T-C

http://identifiers.org/hco/8/GRCh38#27975593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65917881-C-A

27975690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65917783-A-G

27975728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65917729-G-A

27975790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65917666-G-A

27976113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65917371-G-A

27976219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65917277-C-T

27976360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915743-A-G

27976388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915385-G-A

27976413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915363-T-C

27976462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915322-A-G

27976540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915278-T-G

27976556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915262-G-T

27976725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915023-G-A

27976725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65915023-G-T

27976761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65914988-G-A

27976775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65914974-G-C

http://identifiers.org/hco/8/GRCh38#27976781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65914968-C-A

27981284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65914430-G-C

27981780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913978-C-G

27981809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913949-G-C

27981850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913903-C-T

27981884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913883-G-A

27981993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913815-G-A

27982165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913648-C-T

27982282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913507-C-G

27982282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913507-C-T

27982359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913430-A-G

27982612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913190-G-A

27982617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913185-C-T

27982641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913173-C-G

27982641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65913173-C-T

27982883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912943-G-A

27983082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912740-C-T

27983300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912585-G-A

27983308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912577-C-T

27983489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912371-G-A

27983659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912210-G-A

27983659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65912210-G-C

27983948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65910854-T-C

27984003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65910807-C-T

27986664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65908717-T-C

http://identifiers.org/hco/8/GRCh38#27986747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65908644-A-C

27986837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65908550-G-A

http://identifiers.org/hco/8/GRCh38#27987357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65908262-C-A

http://identifiers.org/hco/8/GRCh38#27987375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65908244-C-A

27987379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65908240-A-G

27987439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65908183-G-A

http://identifiers.org/hco/8/GRCh38#27987477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65908146-C-A

27987477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65908146-C-T

27987615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: start lost
orthologous variants: 65908010-T-A

27987655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907977-A-G

http://identifiers.org/hco/8/GRCh38#27987710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65907940-A-C

27987730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907922-G-A

27987730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907922-G-T

http://identifiers.org/hco/8/GRCh38#27987760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65907911-C-A

27987760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907911-C-T

27987898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907888-C-T

http://identifiers.org/hco/8/GRCh38#27988145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65907767-A-C

27988353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907627-G-C

27988433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907563-A-G

27988489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907507-G-A

27988970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65907120-T-C

27989514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906768-T-C

27989601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906670-A-G

27989701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906587-C-G

27989729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906554-C-T

http://identifiers.org/hco/8/GRCh38#27989770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65906510-C-A

27989811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906472-G-C

27989851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906432-A-G

http://identifiers.org/hco/8/GRCh38#27990112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65906225-A-C

27990226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906136-G-A

27990245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65906117-G-T

27990446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65905822-C-T

27990495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65905773-G-T

27990543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65905725-G-T

27990581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65905671-C-T

http://identifiers.org/hco/8/GRCh38#27990729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65905522-C-A

27990729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65905522-C-T

27991160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65905221-T-C

27991422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904995-G-C

27991456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904959-T-C

27991728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904691-C-T

27992121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904321-A-G

http://identifiers.org/hco/8/GRCh38#27992137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65904304-C-A

27992138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904303-T-C

27992159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904281-A-G

27992169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: intron variant
orthologous variants: 65904271-C-T

27992274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5 prime UTR variant
orthologous variants: 65904176-A-G

27992549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5 prime UTR variant
orthologous variants: 65903942-G-A

27992549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28701
most severe consequence: 5 prime UTR variant
orthologous variants: 65903942-G-T