47079731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145051-G-A

47079731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145051-G-T

47079746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145063-C-T

http://identifiers.org/hco/12/GRCh38#47079786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97145069-C-A

47079786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145069-C-T

47079804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97145087-C-T

47079883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145173-G-A

47079883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145173-G-C

47079943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97145225-A-G

47081333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146258-A-G

47081416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146324-T-C

47081864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146745-T-C

47082033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146897-T-C

47082042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146906-G-A

47082058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146922-T-C

47082126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97146987-T-C

47082169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147475-C-G

47082191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147497-C-G

47082301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147590-C-G

http://identifiers.org/hco/12/GRCh38#47082524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97147764-A-C

47082611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147848-A-T

47082677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147907-G-A

47082682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147910-T-C

47082701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97147929-G-T

47082750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97147978-A-G

47082906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97148122-C-T

47083120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97148330-A-G

47085782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97153023-C-G

47085890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97153116-A-G

47086027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97153246-A-G

47086109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97153325-A-G

http://identifiers.org/hco/12/GRCh38#47086267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97153453-A-C

47086331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97153511-T-G

47086611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97154679-G-C

http://identifiers.org/hco/12/GRCh38#47086732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97154801-A-C

47086951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97154967-T-A

47087047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97155067-T-C

47087081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97155100-C-T

47087439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97155396-C-T

47087564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97155521-A-G

http://identifiers.org/hco/12/GRCh38#47087644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97155592-A-C

47087688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97155599-C-T

47087838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97155904-A-G

http://identifiers.org/hco/12/GRCh38#47087912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97155978-C-A

http://identifiers.org/hco/12/GRCh38#47087973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97156074-C-A

47088290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97156371-C-T

http://identifiers.org/hco/12/GRCh38#47088333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97156413-C-A

47088665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97156723-T-C

47090180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158174-A-G

47090202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158193-C-T

47090257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158246-A-G

47090327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158308-A-G

http://identifiers.org/hco/12/GRCh38#47090362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97158344-C-A

47090735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158593-A-G

47090735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158593-A-T

47090753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97158611-C-T

47096893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97167997-A-G

47097265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97168778-A-G

47097364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97168877-C-T

47097486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97168992-T-C

http://identifiers.org/hco/12/GRCh38#47097531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97169037-A-C

47097653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97169149-G-A

47097719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97169217-A-G

47098222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97169739-A-G

http://identifiers.org/hco/12/GRCh38#47098306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97169817-C-A

47098306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97169817-C-G

47098306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97169817-C-T

47098860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97169961-C-G

47099439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97170456-G-C

47099740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97170715-A-G

47099747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97170722-G-A

47099883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97170906-C-T

47100008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97171032-T-A

47100016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97171040-C-T

47100122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97171355-T-C

47101160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97172680-T-C

47101241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97172745-A-G

47102120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97173313-C-T

47102550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97173646-G-T

http://identifiers.org/hco/12/GRCh38#47102859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97173988-A-C

47103073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97174201-A-G

47103258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97174415-G-C

http://identifiers.org/hco/12/GRCh38#47103282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97174439-C-A

47103907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175006-T-C

47103923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175022-G-A

47103923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175022-G-C

47104174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97175276-A-G

47104229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175330-A-G

47104229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175330-A-T

47104235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175336-G-A

http://identifiers.org/hco/12/GRCh38#47104267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97175368-C-A

47104267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97175368-C-T

http://identifiers.org/hco/12/GRCh38#47104779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97176637-A-C

47104779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97176637-A-G

47105074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97176926-T-G

47105884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97177548-C-T

47106457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97178055-T-C

47106547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97178130-G-A

47106547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97178130-G-C

47106637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97178211-A-G

47107252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181018-G-A

47107262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181028-T-A

47107265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181031-C-T

47107311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181074-T-C

47107311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181074-T-G

47107385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181147-G-A

47107385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181147-G-T

http://identifiers.org/hco/12/GRCh38#47107510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97181257-C-A

47107537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181282-G-A

47107537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181282-G-C

47107579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181366-C-T

47107613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181677-G-T

47107646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181730-C-T

47107684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97181775-C-T

47107868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182012-C-T

http://identifiers.org/hco/12/GRCh38#47108060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97182196-C-A

47108397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182505-T-G

47108557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182643-T-C

47108606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182692-A-G

47108709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182772-C-T

47108739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182804-C-T

47108742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97182807-C-G

http://identifiers.org/hco/12/GRCh38#47108930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97182883-A-C

47109078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97183024-T-A

47109085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97183031-A-T

47109119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97183062-T-C

47109278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97183229-G-C

47109936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97183486-T-C

47110240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97183778-A-G

47110582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184511-G-A

47110760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184678-A-T

47110803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184722-C-G

47110855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184776-G-A

47110893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184814-A-G

47110981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184903-T-C

47111033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97184955-C-T

47111211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97185116-A-G

47111233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97185126-T-C

47111989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97186689-G-A

47112198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97186878-A-G

47112385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97187067-G-T

47112448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97187130-G-A

47112472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97187154-A-G

47112513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97187157-T-G

47112588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97187229-A-G

47112817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188318-G-A

47112936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188446-T-C

47112937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188447-G-A

47113088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188562-A-T

47113131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188610-T-C

47113140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188619-C-G

47113181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188651-G-A

47113337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188782-T-C

http://identifiers.org/hco/12/GRCh38#47113474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97188903-C-A

47113490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97188919-T-C

http://identifiers.org/hco/12/GRCh38#47113963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97189206-A-C

http://identifiers.org/hco/12/GRCh38#47114139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97189289-A-C

47114833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97189933-C-T

47114930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97190011-T-C

47115080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97190518-G-A

47115080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97190518-G-C

47115080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97190518-G-T

47115252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97190669-G-T

47115482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97190922-C-T

47115648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97191023-G-A

47115753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97191122-T-C

47116433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97192226-A-T

http://identifiers.org/hco/12/GRCh38#47116480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97192290-A-C

47116735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97192493-C-T

47122418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97193795-C-T

47122720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97194033-G-A

http://identifiers.org/hco/12/GRCh38#47122728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97194041-C-A

47122728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97194041-C-G

47127881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97201858-A-G

47127999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97201989-C-T

47128015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202006-T-A

47128015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202006-T-C

47128033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202020-A-G

47128123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202094-G-A

47128181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202133-G-T

47128468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202357-G-T

47128875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202521-G-A

47128897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202550-G-A

47128928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202578-A-G

47128959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97202615-A-G

47130020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97203513-C-T

47130023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97203516-C-G

47132485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97204770-A-T

47132600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97204873-A-G

47132616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97204890-G-A

47132616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97204890-G-C

http://identifiers.org/hco/12/GRCh38#47136053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97205574-A-C

47136053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97205574-A-T

http://identifiers.org/hco/12/GRCh38#47136054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97205575-C-A

47136054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97205575-C-G

47136054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97205575-C-T

47136200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97205727-G-A

47136288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97205817-C-T

47136438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97205970-G-T

http://identifiers.org/hco/12/GRCh38#47136511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97206043-A-C

47136535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97206067-A-G

47136791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97206231-A-G

http://identifiers.org/hco/12/GRCh38#47136817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97206257-A-C

47137147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97206624-G-A

47137321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97206804-T-C

47137364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97206848-C-G

47138020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97208166-C-G

47138268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97208284-A-G

47138293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97208308-G-A

47138293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97208308-G-C

47138293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97208308-G-T

http://identifiers.org/hco/12/GRCh38#47138382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97208401-C-A

http://identifiers.org/hco/12/GRCh38#47138415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97208434-A-C

http://identifiers.org/hco/12/GRCh38#47138421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97208440-C-A

47140137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97208858-C-T

47140389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209088-G-A

47140530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209232-A-T

http://identifiers.org/hco/12/GRCh38#47140536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97209238-C-A

47140536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209238-C-G

47140536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209238-C-T

47140551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209253-A-G

47140658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209358-G-A

47140959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209592-T-G

47141059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97209682-G-C

http://identifiers.org/hco/12/GRCh38#47141076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97209699-A-C

47148427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212144-A-G

47148596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212264-C-G

http://identifiers.org/hco/12/GRCh38#47148714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97212381-C-A

47148714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212381-C-G

47148714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212381-C-T

47148736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212401-G-A

47148776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212440-T-A

47148806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212470-C-T

47148866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212524-T-A

47148941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212582-T-C

47149087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212706-A-G

47149254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97212870-T-C

47149530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213131-T-G

47149634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213250-G-T

47149642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213258-G-A

47149642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213258-G-C

47149874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213487-A-G

47149880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213493-T-A

47153419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213885-C-T

47153550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97213993-T-C

47153563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214006-A-G

47153583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214028-G-C

47153632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214060-T-C

http://identifiers.org/hco/12/GRCh38#47153666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97214094-C-A

47153764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214182-T-C

47154019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214381-T-C

47154027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214389-A-G

47154034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214396-G-A

47154034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214396-G-C

47154100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214471-T-A

47154100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214471-T-C

47154412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97214764-T-C

47154927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97215162-C-T

http://identifiers.org/hco/12/GRCh38#47154933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97215163-C-A

47154940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97215170-T-A

47155110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97215358-G-A

47155110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97215358-G-C

47155134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97215382-A-G

47155247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97215500-C-G

47155615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97216185-A-G

47155983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97216480-G-A

47156015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97216505-G-A

47156126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97216551-T-A

47156568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97216914-A-T

http://identifiers.org/hco/12/GRCh38#47156652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97216979-A-C

47156652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97216979-A-G

47156786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217103-A-G

47156810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217127-T-C

47156838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217155-C-T

47156875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217199-A-G

47156877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217201-C-T

47156920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217236-A-G

47157018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217326-T-C

http://identifiers.org/hco/12/GRCh38#47157093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97217397-A-C

47157118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217421-C-T

47157190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217488-C-G

http://identifiers.org/hco/12/GRCh38#47157214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97217517-C-A

47157252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217543-C-T

47157295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97217579-G-T

47165192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97222920-T-G

47165280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97223003-A-G

47165442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97223163-T-C

47165500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97223221-A-G

47165592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97223312-A-G

47165609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97223333-T-C

47175116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97229624-A-T

47175148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97229654-G-A

47175369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97229866-A-G

47175461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97229958-T-C

http://identifiers.org/hco/12/GRCh38#47176868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97232610-A-C

47176915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97232651-T-C

47177088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97232792-G-T

47177275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97232928-A-G

47182084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97236516-A-G

47182776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238095-C-G

47182895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238208-T-G

47182908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238221-A-G

47182942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238254-C-T

47182996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238279-A-G

47183030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238309-A-G

47183030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238309-A-T

47183120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97238397-T-C

47184156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97240223-C-T

47184383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97240425-C-T

47184384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97240426-G-A

47184384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97240426-G-T

47184628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97240641-C-T

47188564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97241706-T-G

47188669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97241798-A-G

47189121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97242309-T-G

http://identifiers.org/hco/12/GRCh38#47189175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97242364-A-C

47189453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97242622-A-G

47189507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97242659-G-C

47189614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97242768-A-T

47190283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97244863-C-G

47190420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97244985-C-G

47190420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97244985-C-T

47190461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245024-G-A

http://identifiers.org/hco/12/GRCh38#47190564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97245116-C-A

http://identifiers.org/hco/12/GRCh38#47191383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97245360-A-C

47191419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245395-T-G

47191544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245514-G-A

47191548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245518-G-C

47191552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245522-T-C

47191573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245545-G-A

47191720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245686-C-T

http://identifiers.org/hco/12/GRCh38#47191810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97245760-C-A

47191810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245760-C-G

47191810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245760-C-T

47192058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97245973-A-T

47192540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97246615-T-C

47192804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97246848-A-G

47193024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97247042-T-A

47193024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97247042-T-G

47193655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97248167-C-T

47193675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97248187-G-A

47194444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97248830-A-G

47194615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97248957-T-G

47195734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97249941-G-A

47195938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97250952-T-A

47196108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251104-C-T

47196226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251196-T-G

47196315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251373-C-T

47196316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251374-A-G

47196563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251690-C-G

47196563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251690-C-T

47196626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251743-G-A

http://identifiers.org/hco/12/GRCh38#47196806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97251842-A-C

47196861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97251896-A-G

http://identifiers.org/hco/12/GRCh38#47196902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97251958-C-A

47196959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97252015-T-G

47202194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97254937-T-G

47202455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97255183-A-G

47204898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97256980-G-A

47206706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97258408-A-G

47206734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97258431-T-C

47206846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97258547-C-G

47206862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97258561-C-T

http://identifiers.org/hco/12/GRCh38#47207530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97259106-C-A

47207530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97259106-C-G

47207530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97259106-C-T

47207639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97259183-G-C

47207811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97259325-C-T

47208057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97259539-A-G

47213367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97265400-A-G

47213453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97265493-C-T

47213530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97265574-T-C

47213632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97265647-A-T

47213810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97269232-A-G

47214042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97269426-A-T

47214082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97269466-T-A

47214087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97269471-T-C

47214152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97269540-G-T

47216208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97271604-G-T

http://identifiers.org/hco/12/GRCh38#47216383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97271735-C-A

47216394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97271746-T-C

47216721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97272076-G-T

47216932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97272405-T-C

47216942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97272413-G-C

http://identifiers.org/hco/12/GRCh38#47219924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97273195-A-C

47219924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97273195-A-G

http://identifiers.org/hco/12/GRCh38#47221610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97274043-C-A

47223045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97274640-A-G

47223146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97274681-G-T

47223151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97274686-G-A

47223257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97274790-G-C

47223279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97274798-A-G

47223598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97275091-G-A

47223713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97275217-G-T

47223830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97275319-G-A

47223936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97275389-G-A

47223936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97275389-G-C

47223940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97275393-A-G

http://identifiers.org/hco/12/GRCh38#47223960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97275413-C-A

47224104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, undefined
orthologous variants: 97275494-T-C

47224235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97275674-G-A

47225346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97276393-T-G

47225564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97276652-A-G

47225690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97276958-A-G

47225761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97277032-C-T

47225835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97277109-T-C

47225955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97277207-G-A

47225955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97277207-G-T

http://identifiers.org/hco/12/GRCh38#47226355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97277582-C-A

47232620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280303-C-T

47233979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280901-G-T

47233984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280906-G-C

47233984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280906-G-T

47233991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280913-G-T

47233997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280919-G-T

47234015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97280945-A-G

47234150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281070-G-A

47234194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281191-G-A

47234285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281293-G-A

47234849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281737-G-A

http://identifiers.org/hco/12/GRCh38#47234890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97281773-C-A

47234890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281773-C-T

47234892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281775-T-C

http://identifiers.org/hco/12/GRCh38#47234898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97281781-C-A

47234898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: 97281781-C-T

http://identifiers.org/hco/12/GRCh38#47234925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97281824-C-A

http://identifiers.org/hco/12/GRCh38#47235046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97281945-C-A

47235046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97281945-C-T

47235072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 97281971-T-C

47235121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, missense_variant
orthologous variants: 97282020-A-G

47235121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: intron_variant, missense_variant
orthologous variants: 97282020-A-T

47235603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282502-G-T

47235718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282629-C-T

47235732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: synonymous variant
orthologous variants: 97282643-G-A

47235732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282643-G-T

47235742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282653-T-C

47235811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282722-G-A

http://identifiers.org/hco/12/GRCh38#47235816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97282727-C-A

47235838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282749-C-G

47235838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282749-C-T

47235858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282768-G-T

47235864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282778-G-T

47235933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: synonymous variant
orthologous variants: 97282847-G-A

http://identifiers.org/hco/12/GRCh38#47235959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97282868-A-C

47236012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97282920-T-C

47236114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97283013-G-A

47236114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97283013-G-T

47236116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: synonymous variant
orthologous variants: 97283015-T-C

47236163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97283062-T-G

47236216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: missense variant
orthologous variants: 97283115-C-T

47236245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: synonymous variant
orthologous variants: 97283144-A-G

47236397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97283288-G-A

http://identifiers.org/hco/12/GRCh38#47236436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97283346-C-A

47236525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28255
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97283436-G-A