79382437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 25712175-T-C

79382444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 25712182-C-T

79382581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 25712319-G-A

79382581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 25712319-G-T

79382676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712394-G-T

http://identifiers.org/hco/10/GRCh38#79382683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25712401-C-A

79382683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712401-C-T

http://identifiers.org/hco/10/GRCh38#79382778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25712488-C-A

79382778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712488-C-T

79382950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712613-T-A

79382981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712640-C-G

79382981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712640-C-T

79383173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712830-T-C

http://identifiers.org/hco/10/GRCh38#79383207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25712864-C-A

79383207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25712864-C-G

79383597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713223-A-G

79383798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713430-A-T

79383991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713629-G-A

79383991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713629-G-T

79384007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713643-G-A

79384007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713643-G-C

79384007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713643-G-T

79384125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713716-G-A

79384125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713716-G-T

79384138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713729-G-A

79384180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713752-G-T

79384255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713806-G-C

79384323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713832-G-T

79384331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713839-G-A

http://identifiers.org/hco/10/GRCh38#79384337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25713845-C-A

79384337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713845-C-T

79384341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713849-G-A

79384341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713849-G-T

79384385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713893-G-A

79384385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713893-G-T

http://identifiers.org/hco/10/GRCh38#79384422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25713929-C-A

79384430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713940-G-T

79384488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25713997-G-A

79384507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714016-G-A

http://identifiers.org/hco/10/GRCh38#79384617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25714131-C-A

http://identifiers.org/hco/10/GRCh38#79384710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25714212-C-A

79384717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714219-G-A

79384717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714219-G-T

79384867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714351-C-T

79384870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714354-G-C

79384998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714474-G-T

79385013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714489-T-C

79385108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714578-A-G

79385111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714582-A-T

79385145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714620-G-A

79385145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714620-G-T

79385293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714738-A-G

79385343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714785-G-T

http://identifiers.org/hco/10/GRCh38#79385346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25714788-C-A

79385346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714788-C-T

http://identifiers.org/hco/10/GRCh38#79385363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25714805-C-A

79385373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714815-T-C

79385373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714815-T-G

79385445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714886-C-T

79385564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714956-C-G

79385564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714956-C-T

79385566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25714959-G-T

79385685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715093-T-A

79385685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715093-T-C

http://identifiers.org/hco/10/GRCh38#79385904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25715310-C-A

79385904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715310-C-G

79385904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715310-C-T

79385984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715403-G-A

79385984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715403-G-T

79386015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715434-C-T

http://identifiers.org/hco/10/GRCh38#79386050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25715470-C-A

79386050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715470-C-T

http://identifiers.org/hco/10/GRCh38#79386108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25715510-C-A

79386108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715510-C-T

79386122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715524-G-A

79386122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715524-G-T

http://identifiers.org/hco/10/GRCh38#79386143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25715544-C-A

79386143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715544-C-T

79386144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25715545-T-C

79386483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25715851-C-T

79386531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25715872-A-G

79386597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25715878-T-C

79386704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25715916-G-A

79386787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716000-G-A

79386898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716122-T-C

79387104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716297-C-T

79387379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716603-A-G

79387438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716798-C-T

79387581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716935-G-A

79387581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25716935-G-T

79387646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717019-G-A

79387850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717232-G-A

79387873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717246-C-T

79387876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717249-C-T

79387950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717319-A-G

http://identifiers.org/hco/10/GRCh38#79388215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25717524-A-C

79388242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717540-G-A

79388336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717610-C-T

79388369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717645-C-T

79388387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717663-C-G

79388387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717663-C-T

79388405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717680-C-T

79388674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717917-C-T

79388699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717941-C-T

79388735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25717968-G-C

http://identifiers.org/hco/10/GRCh38#79388797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25718018-C-A

79388843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25718028-G-A

http://identifiers.org/hco/10/GRCh38#79388850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25718035-C-A

79389103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25718202-C-T

79389349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25718407-T-A

http://identifiers.org/hco/10/GRCh38#79389378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25718435-A-C

http://identifiers.org/hco/10/GRCh38#79390246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25718658-A-C

79390502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25718870-A-G

79390635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25718988-G-A

79390653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25719007-C-T

79394285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 25720060-T-A

79394285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 25720060-T-C

79394285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 25720060-T-G

79394452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25720228-G-A

79397642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724342-T-C

79397765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724465-C-G

79398053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724713-G-A

79398107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724750-T-C

79398206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724828-C-T

79398247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724869-G-A

79398308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724921-G-A

79398324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25724937-A-G

79398640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25725176-A-G

79398735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25725290-G-A

79398862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25725369-G-C

79399163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25725619-G-A

79399677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726127-T-C

79399768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726177-G-A

79399804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726183-G-C

79400056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726384-T-C

79400107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726439-G-T

http://identifiers.org/hco/10/GRCh38#79400437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25726638-C-A

79400587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726804-T-C

79400650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726849-G-T

79400722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25726925-C-T

79401109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25727163-G-T

http://identifiers.org/hco/10/GRCh38#79401566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25727401-C-A

79401566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25727401-C-T

http://identifiers.org/hco/10/GRCh38#79401591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25727426-C-A

79401641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25727449-G-C

79401780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25727578-C-T

79401879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25727663-C-T

79402867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25734657-C-T

79402932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25734715-A-G

79402962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25734744-C-T

79403011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25734793-A-G

79403030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25734812-C-T

79403324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735038-G-A

79403365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735113-T-C

79403441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735171-G-A

79403441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735171-G-C

79403441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735171-G-T

79403470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735194-T-C

79403535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735240-C-T

http://identifiers.org/hco/10/GRCh38#79403674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25735376-C-A

79403676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735378-C-T

79404221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25735790-C-T

http://identifiers.org/hco/10/GRCh38#79404248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25735815-C-A

79404531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25736094-T-C

79404541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25736104-A-G

79404766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25736298-G-A

79404953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25736503-C-T

79405233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25736706-C-T

79405866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737243-G-A

79406151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737489-G-A

79406229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737565-G-A

79406271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737606-C-T

79406290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737630-T-C

79406292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737632-G-A

79406348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737710-A-G

79406455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737880-C-G

79406456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737881-T-G

79406509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25737934-C-T

79406980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738337-A-G

79407000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738357-C-T

79407001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738358-A-G

79407132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738486-G-A

79407248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738561-C-T

79407263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738571-G-A

79407384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738711-G-A

79407384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738711-G-T

79407438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25738755-C-T

79407922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25739106-G-A

79408059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25739234-A-G

79408165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25739339-T-C

79408386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25739536-C-T

79408626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25739780-C-T

79408682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25739827-G-C

79409566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25740676-G-A

79409979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25741085-G-A

79409979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25741085-G-T

79410460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25741471-G-C

79410499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25741504-G-A

79410583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25741581-T-C

79410686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25741688-T-A

79412896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25743215-T-A

79413077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25743520-C-T

79413096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25743539-C-T

79413189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25743629-G-A

79413463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25743855-G-A

79413812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744137-A-G

79413812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744137-A-T

79413815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744140-T-G

79413894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744228-A-G

79414034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744355-C-T

79414044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744364-C-T

http://identifiers.org/hco/10/GRCh38#79414091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25744443-C-A

79414267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25744767-C-G

79414627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25745064-A-G

79414735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25745164-A-G

79414852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25745259-T-C

79415610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746154-G-A

79415835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746315-G-A

http://identifiers.org/hco/10/GRCh38#79415989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25746479-C-A

79416221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746726-A-G

79416221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746726-A-T

http://identifiers.org/hco/10/GRCh38#79416270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25746775-C-A

http://identifiers.org/hco/10/GRCh38#79416348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25746847-C-A

79416348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746847-C-T

79416381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746883-C-T

http://identifiers.org/hco/10/GRCh38#79416391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25746893-C-A

79416417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746906-G-C

79416426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746913-G-A

79416436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746923-G-T

79416477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746962-G-A

79416477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25746962-G-T

79418976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747115-A-G

79418978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747117-T-G

79419027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747198-G-A

79419030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747201-C-T

79419083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747319-G-A

79419091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747327-G-A

http://identifiers.org/hco/10/GRCh38#79419234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25747432-C-A

79419234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747432-C-T

79419394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747572-C-G

79419515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25747633-G-A

79419949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748098-G-T

79419987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748134-C-T

79420135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748213-G-T

79420158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748251-C-T

79420218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748312-T-A

79420243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748343-C-G

79420270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748375-G-A

79420359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748458-C-T

79420433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748527-G-T

79420742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748570-C-T

http://identifiers.org/hco/10/GRCh38#79420816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25748602-C-A

79420862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748626-T-C

79421087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25748802-C-T

79421404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25749067-G-A

79422022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25749633-T-A

79422159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25749753-C-T

79422267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25749871-C-T

79422354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25749957-G-A

79422484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25750061-G-A

79422660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25750205-G-T

79423034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25750608-C-T

79423035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25750609-G-A

79423065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25750639-T-C

79423166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25750693-C-G

79424800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25751278-C-T

79424883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25751333-C-T

79425283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25751595-C-T

http://identifiers.org/hco/10/GRCh38#79425512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25751782-C-A

79426054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25752263-T-C

79426684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25752964-A-G

79427103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25753414-C-T

79427611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25753889-G-A

79427656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25753918-A-G

http://identifiers.org/hco/10/GRCh38#79427678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25753938-A-C

79429817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755273-T-A

79429892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755335-G-T

79429895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755338-C-T

79429904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755347-G-A

79429904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755347-G-T

79430054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755485-T-A

79430056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755487-G-C

79430056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755487-G-T

79430296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755658-G-A

79430296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755658-G-C

79430382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755714-C-T

79430525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755812-T-C

http://identifiers.org/hco/10/GRCh38#79430848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25755939-C-A

79430950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755975-T-A

79430952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25755977-C-T

79431027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25756027-T-C

79431577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25756508-T-C

79431694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25756600-G-A

79431861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25756781-T-G

http://identifiers.org/hco/10/GRCh38#79432038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25756960-C-A

79432268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757198-A-G

79432477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757364-T-C

79432502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757387-T-C

http://identifiers.org/hco/10/GRCh38#79432514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25757391-A-C

79432732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 25757609-G-A

http://identifiers.org/hco/10/GRCh38#79432744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25757621-A-C

79432744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 25757621-A-G

79432790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757661-C-T

http://identifiers.org/hco/10/GRCh38#79432830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25757690-C-A

79432830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757690-C-T

79432848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757708-G-A

79432848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757708-G-T

79432951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757761-G-T

79433094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25757870-T-C

79433340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25758412-T-G

79433377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25758446-C-T

79433626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25758693-C-T

79433713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25758777-C-T

79433813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25758860-G-C

79433878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25758920-G-A

79433974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759099-T-C

79433977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759106-G-C

79434074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759249-G-C

79434324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759469-C-T

79434386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759530-G-T

79434446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759563-G-A

79434449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759565-A-G

79434452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759568-G-T

79434459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759575-G-A

79434476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759592-A-T

79434582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25759677-A-G

79434973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760056-T-C

http://identifiers.org/hco/10/GRCh38#79434995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25760067-C-A

79435355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760407-C-T

79435456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760500-A-G

79435457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760501-C-G

79435475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760522-C-T

79435498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760542-C-T

79435734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760764-G-A

79435734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25760764-G-T

79436067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25761022-C-T

79436952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25761234-G-A

79437695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25761625-G-A

79437695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25761625-G-C

79437747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25761677-C-T

79438079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25761979-A-G

79438767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25762607-G-T

79438770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25762610-A-G

79439076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25762913-A-T

79439090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25762927-G-A

79439863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25763442-G-A

79439948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25763525-T-C

79440073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25763648-G-A

79440458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25764207-C-T

79440743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25764538-C-T

79440795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25764616-G-A

79441013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25764825-G-A

79441324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25765223-C-T

79441465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25765488-C-T

79441645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25765723-G-C

79441645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25765723-G-T

79441766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25765853-A-G

79441795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25765882-T-C

79442047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25766118-C-G

79442263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25766300-C-T

79442394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25766402-C-G

79442843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25766818-C-T

79443056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767071-G-A

79443222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767174-C-T

79443447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767364-C-T

79443604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767525-G-A

79443607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767528-C-T

79443958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767879-T-C

http://identifiers.org/hco/10/GRCh38#79443976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25767897-A-C

79443976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767897-A-G

79443976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25767897-A-T

http://identifiers.org/hco/10/GRCh38#79444017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25767953-C-A

http://identifiers.org/hco/10/GRCh38#79444166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25768057-C-A

79444166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25768057-C-T

79444469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25768338-T-C

79444978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25768836-C-G

http://identifiers.org/hco/10/GRCh38#79445095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25768951-C-A

79445095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron variant
orthologous variants: 25768951-C-T

79445170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25769010-G-A

79445172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25769012-C-G

79445172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: intron_variant, undefined
orthologous variants: 25769012-C-T

79445420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: synonymous_variant, undefined
orthologous variants: 25769260-G-A

79445420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: synonymous_variant, undefined
orthologous variants: 25769260-G-T

http://identifiers.org/hco/10/GRCh38#79445568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26911
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25769407-C-A