80779400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5 prime UTR variant
orthologous variants: 83735679-G-A

80779400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5 prime UTR variant
orthologous variants: 83735679-G-T

80779455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5 prime UTR variant
orthologous variants: 83735613-A-G

80779459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5 prime UTR variant
orthologous variants: 83735609-C-T

80779635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735443-G-A

80779635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735443-G-T

http://identifiers.org/hco/15/GRCh38#80779698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83735384-C-A

80779698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735384-C-T

80779793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735291-C-T

80779813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735243-C-G

80779881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735191-G-A

80779916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83735157-C-T

80780183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83734919-G-A

80780266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83734840-T-A

80780835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83734335-C-T

80780863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83734307-C-T

80780882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83734289-G-A

80780913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83734260-G-A

http://identifiers.org/hco/15/GRCh38#80780918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83734255-C-A

80781401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83733782-T-C

80781879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83733351-G-T

80781909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83733324-C-G

http://identifiers.org/hco/15/GRCh38#80782021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83733029-A-C

80782024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83733026-G-A

80782031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83733019-A-G

80782064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83732930-T-C

80782193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83732699-C-G

80782319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83732595-C-G

80782323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83732591-A-G

80782323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83732591-A-T

80782425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83732496-G-A

80782890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83732079-C-T

80783957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83731080-C-G

80784089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730884-C-T

80784149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730810-G-A

80784241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730749-C-G

80784241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730749-C-T

80784339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730648-T-C

80784566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730462-G-C

80784982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83730084-C-G

80785252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83729827-C-T

80785320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83729757-A-G

80785341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83729736-C-T

http://identifiers.org/hco/15/GRCh38#80785630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83729459-A-C

80785858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83729073-A-G

http://identifiers.org/hco/15/GRCh38#80786032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83728887-A-C

80786097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83728824-T-C

http://identifiers.org/hco/15/GRCh38#80786603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83728626-C-A

80786970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83728299-G-A

80786970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83728299-G-T

80787213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83728081-C-G

80787299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83728000-T-A

80787665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83727690-T-A

80787777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83727587-C-T

80787784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83727580-G-A

80787785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83727579-C-T

80787886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83727483-A-G

http://identifiers.org/hco/15/GRCh38#80788646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83726820-A-C

80788936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83726539-G-A

80789494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83725376-T-C

80789672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83725206-G-A

80790013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83724876-T-C

80790085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83724802-T-C

http://identifiers.org/hco/15/GRCh38#80790222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83724673-A-C

http://identifiers.org/hco/15/GRCh38#80790276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83724406-C-A

80790469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83724079-G-A

80790512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83724037-A-G

80790918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83723676-T-G

80791505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83723151-A-T

80791556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83723103-C-T

80791618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83723053-T-C

80791678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83722989-T-C

80791689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83722980-G-A

80794708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83722153-G-A

80794738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83722123-C-T

80794788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83722076-A-G

80795015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83721838-G-C

80795116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83721745-G-T

http://identifiers.org/hco/15/GRCh38#80796288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83721447-A-C

80796369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83721378-A-G

http://identifiers.org/hco/15/GRCh38#80796513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83721236-C-A

80796601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83721153-C-T

80796647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83721106-G-A

80796667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83721086-A-G

80798044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83720275-T-A

80798386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83719159-G-A

80798510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83719006-G-C

80798526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83718990-T-C

http://identifiers.org/hco/15/GRCh38#80799291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83718261-C-A

80799291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83718261-C-T

80799436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83718147-G-T

80800691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717809-T-C

80800824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717693-T-C

80800879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717640-G-A

80800946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717596-C-T

80800984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717558-C-T

http://identifiers.org/hco/15/GRCh38#80801107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83717451-C-A

80801107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717451-C-T

80801197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717363-A-T

80801372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83717187-A-G

http://identifiers.org/hco/15/GRCh38#80801413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83717145-C-A

80802118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83716439-G-C

80802121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83716436-T-A

http://identifiers.org/hco/15/GRCh38#80802495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83716108-C-A

80802653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83715951-G-C

http://identifiers.org/hco/15/GRCh38#80802926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83715679-A-C

80803054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83715562-G-A

80803054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83715562-G-T

80803089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83715519-C-T

80803395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83715306-T-C

80803528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83715170-G-A

80804330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83713241-T-C

80804497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83713098-G-T

80804689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83712909-T-G

80804995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712643-T-C

80805058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712576-C-T

80805073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712561-A-G

80805083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712551-T-A

80805307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712336-T-C

80805418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712223-G-A

80805418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712223-G-T

80805447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83712196-A-G

80805611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83712032-T-C

80805611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83712032-T-G

80805824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83711828-C-T

80805854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83711802-A-G

80805935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83711720-G-T

80806139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83711133-T-C

80806151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83711121-G-T

80806756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83710537-G-A

80806758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83710535-G-A

80806762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83710531-T-C

80808422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83709484-A-T

80808629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83709293-T-C

80808656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83709263-A-G

80808723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83709197-A-G

80809125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83708781-T-C

http://identifiers.org/hco/15/GRCh38#80809132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83708694-C-A

80809498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83708302-A-G

80810233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83708033-A-T

80810262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83708001-A-G

http://identifiers.org/hco/15/GRCh38#80810931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83707656-C-A

80810983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83707609-C-G

80812209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83707022-G-A

80812258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83706980-C-T

80812458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83706147-G-T

80812557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83706027-C-G

80812557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83706027-C-T

80812868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83705724-G-T

80812950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83705623-A-T

80814501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83705168-T-A

80814752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83704943-A-G

80814814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83704888-C-T

80815619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83703698-C-T

http://identifiers.org/hco/15/GRCh38#80815713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83703600-C-A

80815715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83703599-T-C

80815766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83703486-G-A

80815790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83703462-T-C

80815845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83703409-A-G

80815972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83703283-T-A

http://identifiers.org/hco/15/GRCh38#80816611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83702964-A-C

80816729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83702848-G-A

80816859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83702721-G-A

80817176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83702435-G-A

80817176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83702435-G-T

80818191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83701802-A-G

80818245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83701763-A-G

80818403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83701641-T-A

80818416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83701627-T-G

80818487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83701550-A-G

80818626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83701430-C-T

80818720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83701343-T-C

80819117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83700932-G-A

80819258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83700791-G-C

80819309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83700735-T-C

80819330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83700715-G-A

80819411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83700633-C-T

80819632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83700412-T-C

80819632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83700412-T-G

80819902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83700178-A-G

80820090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83700015-G-A

80820361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83699763-T-G

80820670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83699488-G-A

80821120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83695648-C-T

80821262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83695515-C-G

80821660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83695100-G-A

80821872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694894-G-A

80821874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694892-A-G

http://identifiers.org/hco/15/GRCh38#80821966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83694798-A-C

80821967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694797-C-T

80822230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694529-G-A

80822297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694466-C-T

80822454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694307-G-A

80823030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693766-T-C

80823033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693763-G-A

80823151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693657-A-G

80823559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693289-T-C

http://identifiers.org/hco/15/GRCh38#80823691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83693163-C-A

80823717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693138-T-C

80824564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83692999-G-A

80824763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83692860-T-C

80824779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83692844-A-T

80825069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83692572-A-T

80825428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83692265-C-T

http://identifiers.org/hco/15/GRCh38#80825605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83692088-A-C

80826251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691706-A-G

80826382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691605-T-G

80826685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691343-G-A

80826797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691248-G-A

http://identifiers.org/hco/15/GRCh38#80830995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83691080-C-A

80830995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83691080-C-G

80831281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83690807-G-A

80831556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83690601-A-G

80831667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83690490-C-G

80831766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83690373-T-C

80831842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83690306-C-T

80832244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689960-A-T

80832278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689925-C-G

80832297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689906-C-T

80832324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689879-G-C

80832338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689865-G-C

80832408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689661-G-A

80832411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83689658-T-A

http://identifiers.org/hco/15/GRCh38#80835389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83687700-C-A

80835389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83687700-C-T

80835520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83687590-C-T

80835524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83687586-T-G

80835775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83687336-C-T

80836230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686905-G-A

80836369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686786-G-A

http://identifiers.org/hco/15/GRCh38#80836547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83686494-C-A

80836547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686494-C-T

80836695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686285-C-T

80836713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686268-G-C

80836789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686198-G-A

80836789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686198-G-C

80836789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686198-G-T

80836791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686196-G-T

http://identifiers.org/hco/15/GRCh38#80836797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83686190-A-C

80836865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83686134-G-A

80837126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83685914-G-A

80837532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83685523-C-T

80837696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83685357-A-G

80837804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83685242-G-T

80837888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83685164-G-A

80837888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83685164-G-C

http://identifiers.org/hco/15/GRCh38#80837954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83685128-A-C

80838109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683131-G-A

80838301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682970-C-T

80838323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682948-C-T

80838336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682935-C-T

80838432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682839-G-C

http://identifiers.org/hco/15/GRCh38#80838552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83684956-A-C

80838740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83684805-A-G

80838740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83684805-A-T

80838765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83684780-C-G

80838885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83684664-G-C

80839074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83684514-G-A

80839261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83684335-G-A

80839334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83684234-A-G

80839334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83684234-A-T

http://identifiers.org/hco/15/GRCh38#80839457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83683892-C-A

80839603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683738-T-C

80839821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683496-C-T

80839888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683424-A-T

80839957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683370-A-G

80840026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683293-G-T

80840214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83683131-G-C

80840407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682970-C-G

80840407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682970-C-T

80840442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682935-C-T

80840538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682839-G-A

80840647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682745-T-A

80840869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682512-C-T

80841323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682110-A-T

80841366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682063-G-C

80841415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682014-G-A

80841416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83682013-G-T

80841710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83681668-G-A

80841751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83681643-A-G

80841878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83681505-T-C

80841959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83681428-G-A

80841959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83681428-G-T

80843240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83679689-C-T

80843313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83679627-T-C

80843423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83679526-C-T

80844204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83678805-G-C

80844328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83678673-T-A

80844502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83678520-T-C

80844586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83678437-T-G

http://identifiers.org/hco/15/GRCh38#80844588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83678435-A-C

80844694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83678341-A-G

80844729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83678307-A-G

80844754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83678282-G-A

80844775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83678261-T-A

80845656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83677913-T-C

80845889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83677678-C-T

80845928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83677635-G-T

80845946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83677617-C-T

80845977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83677589-G-A

80846156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83677432-C-T

80850109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83673979-G-T

80851175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 83673805-G-A

http://identifiers.org/hco/15/GRCh38#80851200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83673780-C-A

80851200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83673780-C-T

80851354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83673654-C-T

80851422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83673586-G-A

80851786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83673132-A-T

80851984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83672954-T-C

80852082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83672883-T-C

80852082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83672883-T-G

http://identifiers.org/hco/15/GRCh38#80852236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83672655-A-C

80852704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83672195-T-C

80852876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83672048-G-A

80853185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83671798-A-G

80853301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83671703-G-C

80853360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83671656-A-T

80853670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83671379-C-T

80853934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83671125-T-C

80854234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83670403-G-A

http://identifiers.org/hco/15/GRCh38#80854454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83670227-C-A

80854454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83670227-C-T

80854489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83670189-C-G

80854505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83670173-A-G

80854559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83670128-C-G

80854559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83670128-C-T

80856234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83668614-G-A

80856263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83668585-T-A

80856448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83668407-T-C

80857203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83667739-G-A

80857405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83667531-G-A

80857405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83667531-G-C

80857506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83667433-A-G

http://identifiers.org/hco/15/GRCh38#80857580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83667374-A-C

80857855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83667116-G-T

80857875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83667096-A-G

80857918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83667050-G-A

80858176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83666859-G-A

80858747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83666235-C-T

80859143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83665876-A-T

80859190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83665846-G-A

80859205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83665831-C-T

80859378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83665631-C-G

80859641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83665271-C-T

http://identifiers.org/hco/15/GRCh38#80859716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83665194-C-A

80859951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83664991-G-A

80860030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83664924-C-T

80860346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83664425-T-C

80860551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83664248-C-T

80860901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663961-G-A

80860930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663921-C-T

80860976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663875-C-G

80861162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663695-C-T

80861168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663689-G-A

80861275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663538-G-T

80861604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663299-A-G

80861686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663222-A-G

80861837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83663093-G-T

80862258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662823-T-C

80862258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662823-T-G

80862354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662734-T-C

80862362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662726-G-A

80862446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662637-T-A

http://identifiers.org/hco/15/GRCh38#80862465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83662621-C-A

80862465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662621-C-T

80862476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662610-T-C

80862477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662609-C-G

http://identifiers.org/hco/15/GRCh38#80862596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83662513-A-C

80862666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662441-C-T

80862785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662312-G-A

80862812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662285-G-A

80862832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662265-C-G

80862877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83662226-C-T

80863176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83661945-G-A

80863176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83661945-G-T

80863207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83661904-T-G

80863331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83661793-A-G

80863866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83660300-G-A

80863875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83660291-T-C

80863889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83660277-A-G

80863901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83660265-T-G

http://identifiers.org/hco/15/GRCh38#80864372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83659834-A-C

http://identifiers.org/hco/15/GRCh38#80864378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83659828-C-A

80864406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83659807-G-T

80864953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83659330-G-A

80864957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83659326-A-G

80864966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83659314-C-T

80864972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83659308-G-A

80866963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83658040-T-G

80867498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83657233-C-T

80867810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83656940-T-C

80867810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83656940-T-G

80869899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83655802-A-G

80870269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83655442-G-C

80870333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83655394-A-G

80870383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83655347-G-T

80870407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83655323-T-A

http://identifiers.org/hco/15/GRCh38#80870408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83655322-C-A

80870526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83655210-G-T

80870595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83655154-C-T

80870699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83655115-G-A

80870700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83655114-G-A

80870763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83655055-T-G

80871065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83654784-C-G

80871065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83654784-C-T

80871150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83654703-T-C

80871312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83654565-G-A

80871331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83654549-T-C

80871943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653916-C-G

80872072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653815-G-A

80872167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653734-A-G

80872411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653530-C-T

http://identifiers.org/hco/15/GRCh38#80872520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83653450-C-A

80872520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653450-C-T

http://identifiers.org/hco/15/GRCh38#80872946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83653324-C-A

80872946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653324-C-T

80872979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653295-G-A

80873029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653245-G-A

80873032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653242-G-A

80873204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83653100-G-T

80873455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652970-A-G

80873463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652961-G-A

80873463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652961-G-T

80873470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652954-G-C

80873470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652954-G-T

http://identifiers.org/hco/15/GRCh38#80873491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83652933-C-A

80873512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652927-T-A

80873512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652927-T-G

80873614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652848-T-C

80873669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83652793-T-G

80873779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, stop_gained
orthologous variants: 83652692-G-A

80873779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, missense_variant
orthologous variants: 83652692-G-C

80873779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, missense_variant
orthologous variants: 83652692-G-T

80873866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 83652625-A-G

80873866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 83652625-A-T

http://identifiers.org/hco/15/GRCh38#80873895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83652596-A-C

80873895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83652596-A-G

http://identifiers.org/hco/15/GRCh38#80873927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83652564-C-A

80873927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: synonymous variant
orthologous variants: 83652564-C-T

80873959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83652532-G-A

80873959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83652532-G-C

80873959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83652532-G-T

80874043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652477-T-C

80874199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652348-T-C

80874234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652319-C-T

80874290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652268-C-T

80874400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652165-T-C

http://identifiers.org/hco/15/GRCh38#80874430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83652139-C-A

80874501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652077-T-C

80874550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83652031-C-T

80874687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651561-G-C

80874746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651503-G-A

80874770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651479-G-A

80874815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651440-C-T

80874946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651319-T-C

http://identifiers.org/hco/15/GRCh38#80874989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83651278-C-A

80874989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651278-C-T

80875003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83651264-G-C

80875714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83650932-T-C

80875929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83650740-A-G

80875929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83650740-A-T

http://identifiers.org/hco/15/GRCh38#80876055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83650602-C-A

80876055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83650602-C-T

80876701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83650080-G-A

80876759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83650049-G-A

http://identifiers.org/hco/15/GRCh38#80878648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83648532-C-A

80878704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83648478-C-T

80878722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 83648460-G-T

80878954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83648246-G-T

80878974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83648226-G-C

80878996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83648202-T-C

80879002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83648196-T-A

80879124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: 83648070-T-C

80879637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647915-G-C

http://identifiers.org/hco/15/GRCh38#80879692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83647857-C-A

80879692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647857-C-T

http://identifiers.org/hco/15/GRCh38#80879757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83647794-C-A

80879757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: stop gained
orthologous variants: 83647794-C-T

80879919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647632-G-C

80879919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647632-G-T

80879956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647596-G-A

80879956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647596-G-T

http://identifiers.org/hco/15/GRCh38#80879973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83647577-C-A

80879980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647570-G-C

80879980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83647570-G-T

80880733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83646821-C-G

80880754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83646801-A-G

80881072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83646492-G-A

80881240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83646345-G-A

80881240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83646345-G-C

80881240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83646345-G-T

80881484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83646084-A-T

80881747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83645888-A-G

80883440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83642069-G-C

80883474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83642035-A-G

80883541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641960-A-G

http://identifiers.org/hco/15/GRCh38#80883706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83641865-C-A

http://identifiers.org/hco/15/GRCh38#80883844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83641726-A-C

http://identifiers.org/hco/15/GRCh38#80884058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83641526-C-A

80884071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641511-T-A

80884071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641511-T-C

http://identifiers.org/hco/15/GRCh38#80884082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83641501-C-A

80884082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641501-C-T

80884110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641475-G-A

80884110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641475-G-C

80884110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641475-G-T

80884124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641461-G-A

80884124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641461-G-C

80884169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83641409-T-C

80884275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83641303-G-A

80884498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83641107-T-C

80884607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640960-T-A

80884612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640955-C-T

http://identifiers.org/hco/15/GRCh38#80884752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83640813-C-A

80884752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640813-C-T

80884756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640809-G-A

80885172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640638-G-A

80885172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640638-G-T

80885174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640636-A-G

80885444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640388-T-C

80885459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640373-G-A

80885563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83640269-C-T

80885941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639934-T-C

80886279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639656-T-C

80886300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639638-G-A

80886450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639492-A-G

80886551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639416-A-T

80886781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639190-G-A

80886994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639045-T-C

80887002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83639037-T-G

http://identifiers.org/hco/15/GRCh38#80887054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83638987-C-A

80887054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638987-C-T

80887296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638774-G-C

80887340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638749-C-T

80887350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638739-G-T

80887384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638705-A-G

80887446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638645-G-A

80887535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638552-G-A

http://identifiers.org/hco/15/GRCh38#80887568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83638518-C-A

http://identifiers.org/hco/15/GRCh38#80887807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83638296-C-A

80887807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638296-C-T

80887895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638212-G-A

80887895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638212-G-C

80887895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83638212-G-T

80888593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637449-G-C

80888593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637449-G-T

80888612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637352-G-A

80888612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637352-G-T

80888614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637350-G-A

80888614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637350-G-C

80888709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83637253-G-A

80888969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83637017-G-A

http://identifiers.org/hco/15/GRCh38#80889017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83636971-C-A

80889122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83636876-A-T

80889132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83636869-C-T

80889651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83636486-T-C

80889695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83635637-G-A

80889695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83635637-G-C

http://identifiers.org/hco/15/GRCh38#80889846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83635504-C-A

80893237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83634545-T-C

80893484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83634330-G-A

80893791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83634065-C-T

80894132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83633702-G-T

80894137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83633697-C-G

80894137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83633697-C-T

80894293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83633603-A-G

80894331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83633565-G-A

80894520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83633370-G-A

80894847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632614-G-T

80894850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632611-A-G

http://identifiers.org/hco/15/GRCh38#80894851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83632610-A-C

80894935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632525-T-A

80894935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632525-T-C

80895124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: splice donor variant
orthologous variants: 83632338-T-C

http://identifiers.org/hco/15/GRCh38#80895132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83632319-C-A

80895132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632319-C-T

http://identifiers.org/hco/15/GRCh38#80895195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83632238-C-A

80895230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632189-G-A

80895430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83632021-T-C

80895760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83631698-G-C

80895760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83631698-G-T

80895794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83631664-A-G

80896080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83631384-C-T

80896082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83631382-T-C

80899510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630958-C-T

80899654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630799-A-G

80899663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630790-G-A

80899668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630785-T-C

80899821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630669-G-T

80899991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630556-A-G

80900007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630540-C-T

80900080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630482-C-T

80900215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630358-C-T

80900249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630327-G-A

http://identifiers.org/hco/15/GRCh38#80900678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83630014-A-C

80900678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630014-A-G

80900678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630014-A-T

80900690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83630002-T-C

http://identifiers.org/hco/15/GRCh38#80900790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83629913-C-A

http://identifiers.org/hco/15/GRCh38#80900821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83629877-C-A

http://identifiers.org/hco/15/GRCh38#80901006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83629707-C-A

80901006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629707-C-T

80901046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629665-A-G

80901071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629640-G-C

80901071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629640-G-T

80901104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629599-C-T

80901110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629593-T-C

80901254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629460-C-T

80901334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629381-C-T

80901767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629258-G-A

80901863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629171-C-G

80901996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629047-C-T

80902044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83629000-T-A

80902064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628980-T-C

80902064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628980-T-G

80902097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628956-C-T

80902165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628888-T-C

80902302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628782-T-C

80902446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628658-T-A

80902798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628369-G-A

80902944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628229-G-A

80902965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628208-A-G

80902971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628202-T-C

80903058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83628039-G-T

80903095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 83627937-A-G

80903130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83627893-G-T

80903253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627752-T-C

http://identifiers.org/hco/15/GRCh38#80903255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83627750-A-C

80903255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627750-A-G

80903263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627745-T-C

80903313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627679-T-C

80903313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627679-T-G

http://identifiers.org/hco/15/GRCh38#80903353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83627639-A-C

80903357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627635-T-C

http://identifiers.org/hco/15/GRCh38#80903454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83627514-C-A

80903843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83627031-G-A

80904507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83626429-G-A

80904595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83626344-G-A

80904637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83626304-G-C

80904935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83626037-C-T

80905014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83625972-A-T

80905316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83625677-G-C

80905776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83625354-G-A

80905804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83625331-A-G

80905966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83625197-G-C

80906308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624783-C-G

80906308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624783-C-T

80906378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83624712-C-G

80906535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624557-A-G

80906548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624537-G-C

80906562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624515-G-A

80906562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624515-G-T

80906568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624509-A-G

http://identifiers.org/hco/15/GRCh38#80906580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83624497-C-A

80906616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624468-G-A

http://identifiers.org/hco/15/GRCh38#80906631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83624453-C-A

80906631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83624453-C-T

80906818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 83624266-A-G

80906907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83624179-G-A

80907689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83623852-C-T

80908059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83623480-A-G

80908479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83623151-A-G

80908993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83622711-A-G

80909023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83622674-G-T

80909042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83622641-G-T

80909052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83622631-A-G

80909068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83622616-T-C

80909100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83622585-G-A

80909100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83622585-G-T

80909160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83622525-C-G

80912322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83622263-T-C

80912561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83621996-T-C

80912563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83621995-G-A

80912563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83621995-G-T

80912715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83621893-T-G

80912937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83621638-T-A

80913097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83621478-T-C

80913680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83620647-A-G

80913827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83620526-G-A

80913949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83620387-C-T

80913992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83620339-A-G

80914153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83620136-C-T

80914233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83620069-G-A

http://identifiers.org/hco/15/GRCh38#80915729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83619388-A-C

80915920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83619214-T-A

80916126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83617455-A-G

80916213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83617359-G-A

80916722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83616043-A-G

80916745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83616020-A-T

80916905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83615885-G-A

80916990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83615838-C-T

80917610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83615323-G-A

http://identifiers.org/hco/15/GRCh38#80917624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83615303-C-A

80917755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83615169-T-C

80918417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83614679-T-C

80919135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83614111-C-T

80919641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613834-G-C

80919641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613834-G-T

80919802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613636-G-A

80919998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613483-A-G

80920034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613454-A-G

80920093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: splice acceptor variant
orthologous variants: 83613398-G-A

80920093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: splice acceptor variant
orthologous variants: 83613398-G-C

80920217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83613274-T-A

80920334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613130-G-A

80920334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613130-G-T

80920350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613114-G-A

80920350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613114-G-T

80920416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613030-G-A

80920416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83613030-G-T

80920518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83612961-T-C

80920629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83612756-G-A

80920941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83612415-A-G

http://identifiers.org/hco/15/GRCh38#80920954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83612404-C-A

80921005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83612346-T-C

80921136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83612228-A-G

http://identifiers.org/hco/15/GRCh38#80921206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83612181-C-A

80921299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83612141-A-G

80921375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83611524-T-C

80921582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83611346-C-T

80921806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83611099-A-G

80921832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83611073-C-T

80921852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83611055-A-G

80921956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610933-G-A

80922274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610644-G-A

80922274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610644-G-T

80922279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610639-G-A

80922279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610639-G-T

80922283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610635-T-C

80922288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610630-G-A

80922288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610630-G-C

80922288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610630-G-T

80922357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610576-T-C

80922832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610152-T-C

80922887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610092-G-A

80922909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83610025-C-T

80922935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83609861-C-T

80923044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83609713-C-T

80923350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83609473-G-C

80923412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83609423-G-C

80923779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83609028-A-G

80923861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83608944-C-T

80923887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83608920-G-C

80924061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83608732-C-T

http://identifiers.org/hco/15/GRCh38#80924316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83608320-A-C

80924390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83608064-T-G

80924486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607922-A-G

80924486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607922-A-T

80924492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607916-G-A

80924492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607916-G-T

80924509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607899-A-T

80924553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607857-T-C

80924554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607856-G-T

80924572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607839-G-A

80924639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83607782-A-G

80924660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83607761-G-C

80924712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607710-C-T

80924726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607697-A-T

80924749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607674-G-A

http://identifiers.org/hco/15/GRCh38#80924751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83607672-C-A

80924751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607672-C-G

http://identifiers.org/hco/15/GRCh38#80924761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83607664-C-A

80924761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607664-C-T

http://identifiers.org/hco/15/GRCh38#80924826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83607610-C-A

80924837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607599-T-A

80924837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607599-T-C

80924837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607599-T-G

80924946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607490-G-A

80924985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607448-G-A

80925001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607432-C-G

80925001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607432-C-T

80925053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83607386-A-T

http://identifiers.org/hco/15/GRCh38#80925526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83606991-C-A

80925526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606991-C-T

80925563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606954-G-T

http://identifiers.org/hco/15/GRCh38#80925606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83606936-C-A

80925606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606936-C-G

80925606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606936-C-T

80925795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606755-A-G

80925813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606738-G-C

80925813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606738-G-T

80926125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606451-C-G

80926125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606451-C-T

80927602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606126-G-A

80927671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83606059-T-G

80928057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83605325-C-T

80928083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83605298-G-C

80928108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83605270-G-A

80928108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83605270-G-T

80928246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83605193-C-T

http://identifiers.org/hco/15/GRCh38#80928377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83605187-C-A

80928756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604822-T-C

80928756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604822-T-G

80928834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604763-T-C

80928967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604634-T-C

80928968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604633-C-T

80928987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604614-G-A

80929192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604408-T-C

80929251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604336-G-A

80929251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83604336-G-C

http://identifiers.org/hco/15/GRCh38#80929298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83604295-A-C

80930193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603875-A-G

80930193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603875-A-T

80930349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603737-A-G

80930440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603672-C-T

80930502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603627-G-T

80930592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603542-G-A

80930615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603519-C-G

80930626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603508-T-C

http://identifiers.org/hco/15/GRCh38#80930647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83603488-A-C

80930736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603433-T-C

80930958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603209-G-A

80931029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603135-G-A

80931089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83603095-C-T

80931211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83602968-C-T

80931298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83602889-C-G

80931606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83602452-C-T

80931664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83602338-T-A

80931932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83602100-G-A

80931932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83602100-G-C

80931938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83602094-C-G

80931953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83602079-A-G

http://identifiers.org/hco/15/GRCh38#80932050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83601982-C-A

80932050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601982-C-T

80932166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601866-G-A

80932166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601866-G-C

80932166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601866-G-T

http://identifiers.org/hco/15/GRCh38#80932173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83601859-C-A

80932173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601859-C-G

http://identifiers.org/hco/15/GRCh38#80932353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83601729-A-C

80932491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601596-C-G

http://identifiers.org/hco/15/GRCh38#80932587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83601517-C-A

80932598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601475-T-C

80932684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601346-G-A

80932811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601211-C-T

80933038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601030-C-G

80933068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83601000-T-A

80933077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600991-G-A

http://identifiers.org/hco/15/GRCh38#80933143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83600926-C-A

80933208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600861-C-G

80933212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600857-T-G

80933353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83600716-T-C

http://identifiers.org/hco/15/GRCh38#80933471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83600598-C-A

http://identifiers.org/hco/15/GRCh38#80933499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83600568-C-A

80933499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600568-C-G

80933499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600568-C-T

80933522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600547-G-T

80933534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600535-T-C

http://identifiers.org/hco/15/GRCh38#80933612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83600462-C-A

80933612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600462-C-T

80933799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600321-C-G

80933817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83600303-G-T

http://identifiers.org/hco/15/GRCh38#80934395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83599585-C-A

80934601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83599386-G-A

80934727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83599261-G-T

80934920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83599124-G-A

80934982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83599063-A-G

80935108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83598958-G-A

80935269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83598825-A-G

80936538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83598118-T-G

80936568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83598102-G-A

80936568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83598102-G-C

80936568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83598102-G-T

80936807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83597864-C-T

http://identifiers.org/hco/15/GRCh38#80936824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83597847-A-C

80936824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83597847-A-G

80936848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: missense variant
orthologous variants: 83597823-C-T

http://identifiers.org/hco/15/GRCh38#80936899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83597759-C-A

80936899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597759-C-T

http://identifiers.org/hco/15/GRCh38#80936959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83597686-C-A

80936959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597686-C-G

80936959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597686-C-T

80936975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597670-A-G

http://identifiers.org/hco/15/GRCh38#80936992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83597653-C-A

80936992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597653-C-G

80937002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597644-G-A

80937002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597644-G-T

http://identifiers.org/hco/15/GRCh38#80937022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83597624-C-A

80937022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597624-C-T

80937175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597494-A-G

80937278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83597385-C-T

80937548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83596739-G-T

http://identifiers.org/hco/15/GRCh38#80938038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83596299-C-A

http://identifiers.org/hco/15/GRCh38#80938059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83596278-C-A

80938059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83596278-C-G

80938109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83596228-G-A

80938109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83596228-G-T

80938114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83596223-T-A

80938140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83596201-G-A

80938140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 83596201-G-T

80938199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83596145-T-G

80940054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83595108-C-T

80940252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594992-G-A

80940253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594991-T-C

80940645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594640-G-T

80940790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594456-A-G

80940837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594404-T-C

80940952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594284-T-G

80941064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83594162-C-T

80941444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593858-G-C

80941611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593707-G-A

http://identifiers.org/hco/15/GRCh38#80941737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83593521-C-A

80941744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593512-G-A

80941797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593345-G-A

80941797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593345-G-C

80941797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593345-G-T

80941806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593336-T-G

80941832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593309-A-T

80942018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83593123-G-A

80942018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 83593123-G-C

80942098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593072-G-A

80942098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593072-G-T

80942107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83593065-G-A

80942299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83592863-C-T

80942323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83592839-T-C

80942323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83592839-T-G

80942343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83592819-T-A

80942343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83592819-T-C

80942377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83592790-T-C

80942569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83591753-T-C

80942679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83591640-A-G

http://identifiers.org/hco/15/GRCh38#80942798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83591533-C-A

80942798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83591533-C-G

80942798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83591533-C-T

80942807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 83591524-A-T

http://identifiers.org/hco/15/GRCh38#80942886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83591432-C-A

http://identifiers.org/hco/15/GRCh38#80942911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83591409-C-A

80942996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 83591318-A-G

http://identifiers.org/hco/15/GRCh38#80943331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83590993-C-A

80943669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83590676-C-T

80944726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83589696-C-T

80944744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83589678-T-C

http://identifiers.org/hco/15/GRCh38#80944816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83589595-A-C

80945202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83589241-G-A

80945645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83588852-C-T

80945667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83588830-G-A

80945667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83588830-G-C

http://identifiers.org/hco/15/GRCh38#80945987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83588496-C-A

80945987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83588496-C-T

80946069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: intron variant
orthologous variants: 83588427-C-T

80946735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83586912-G-T

80946772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83586886-A-T

http://identifiers.org/hco/15/GRCh38#80946848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586811-C-A

80946848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83586811-C-G

80946848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83586811-C-T

80946857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83586798-G-A

80946857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83586798-G-T

http://identifiers.org/hco/15/GRCh38#80946895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586764-C-A

80947126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586544-T-C

80947158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586514-A-G

80947158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586514-A-T

80947163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586509-G-A

http://identifiers.org/hco/15/GRCh38#80947267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586415-C-A

http://identifiers.org/hco/15/GRCh38#80947298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586386-A-C

80947298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586386-A-G

80947316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586368-T-C

80947424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586280-G-T

80947472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586233-G-A

http://identifiers.org/hco/15/GRCh38#80947520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586168-C-A

80947520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586168-C-T

80947542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586156-C-T

80947545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586153-G-T

80947618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586079-A-G

http://identifiers.org/hco/15/GRCh38#80947622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586075-C-A

80947622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83586075-C-T

http://identifiers.org/hco/15/GRCh38#80947701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83586003-C-A

80947734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585976-G-C

80947734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585976-G-T

80947760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585951-T-G

80947885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585830-G-T

80948053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585670-T-G

80948129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585596-G-T

80948177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585550-T-A

80948177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585550-T-C

http://identifiers.org/hco/15/GRCh38#80948196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83585525-C-A

80948196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585525-C-G

80948258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585473-A-G

http://identifiers.org/hco/15/GRCh38#80948364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83585382-A-C

80948364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585382-A-G

http://identifiers.org/hco/15/GRCh38#80948454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83585303-C-A

80948454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585303-C-G

80948454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585303-C-T

80948469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585289-G-A

80948469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585289-G-T

80948521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585237-C-T

80948552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585206-A-T

80948624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585133-T-C

80948624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585133-T-G

80948652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585105-G-T

80948666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585091-G-A

http://identifiers.org/hco/15/GRCh38#80948670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83585087-C-A

80948670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585087-C-T

80948674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585083-G-A

80948674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585083-G-C

http://identifiers.org/hco/15/GRCh38#80948690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83585067-C-A

80948690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585067-C-T

80948732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585022-G-T

80948736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585018-G-A

80948736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83585018-G-T

80948811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83584940-G-A

80948811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83584940-G-C

80948856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83584895-A-T

80948924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 83584827-A-G

http://identifiers.org/hco/15/GRCh38#80948981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83584783-C-A

80948981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83584783-C-T

http://identifiers.org/hco/15/GRCh38#80948986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83584778-C-A

80948986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83584778-C-T

80949203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83584609-T-C

80949237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83584577-T-C

http://identifiers.org/hco/15/GRCh38#80949482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83584331-C-A

80949482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83584331-C-T

http://identifiers.org/hco/15/GRCh38#80949696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83584128-C-A

80949696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83584128-C-T

80949901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583920-C-T

80950054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583774-C-G

80950177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583651-G-A

80950177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583651-G-T

80950234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583581-G-A

80950234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583581-G-T

80950372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583464-C-T

http://identifiers.org/hco/15/GRCh38#80950479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83583291-C-A

80950694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583090-G-A

http://identifiers.org/hco/15/GRCh38#80950760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83583055-C-A

80950764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83583051-T-C

80950886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582931-A-T

http://identifiers.org/hco/15/GRCh38#80950897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83582920-C-A

80950897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582920-C-T

80950932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582884-G-A

80950932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582884-G-T

80950938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582878-A-T

80951090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582727-A-G

80951100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582717-G-A

80951124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582683-T-C

http://identifiers.org/hco/15/GRCh38#80951321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83582496-A-C

80951351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582466-C-T

80951694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582139-G-A

80951694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83582139-G-T