104137111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111265-A-G

104137113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111280-A-T

http://identifiers.org/hco/14/GRCh38#104137126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112111293-C-A

104137126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111293-C-G

104137126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111293-C-T

104137145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111314-G-A

104137145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111314-G-T

http://identifiers.org/hco/14/GRCh38#104137149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112111318-C-A

104137149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111318-C-T

104137326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111457-G-A

http://identifiers.org/hco/14/GRCh38#104137335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112111466-C-A

104137335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111466-C-G

104137335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111466-C-T

104137344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111476-T-A

104137344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111476-T-G

104137371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111506-A-G

104137479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111606-G-A

104137479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111606-G-T

104137526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111650-T-C

104137526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111650-T-G

104137742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111884-C-T

104137752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112111894-T-C

104137922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112112073-G-A

104137922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112112073-G-T

http://identifiers.org/hco/14/GRCh38#104137968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112112121-C-A

104137968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112112121-C-T

104138298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112112422-A-G

104138582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112112679-G-A

104138582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112112679-G-T

http://identifiers.org/hco/14/GRCh38#104138590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112112687-C-A

104138590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 112112687-C-T

http://identifiers.org/hco/14/GRCh38#104138664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112112760-C-A

104138664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112112760-C-G

104138664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112112760-C-T

104138839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112112930-T-C

104138918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113002-G-T

104139024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113129-C-T

http://identifiers.org/hco/14/GRCh38#104139059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112113164-C-A

104139059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 112113164-C-G

104139059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 112113164-C-T

http://identifiers.org/hco/14/GRCh38#104139222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112113324-C-A

104139222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 112113324-C-T

104139307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113409-G-T

http://identifiers.org/hco/14/GRCh38#104139319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112113419-C-A

104139319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113419-C-G

104139319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113419-C-T

104139397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113489-T-C

104139451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113513-C-T

104139604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113654-G-C

104139735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113736-G-C

104139877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113887-G-A

104139969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112113976-G-A

104140399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112114358-T-C

104140623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112114507-G-A

104141190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112114995-G-C

104141407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112115200-G-C

104142607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112115635-C-T

http://identifiers.org/hco/14/GRCh38#104142623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112115648-A-C

104142755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112115792-C-T

104142771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112115809-C-G

104142833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112115866-T-A

104142978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116002-C-T

104143026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116032-G-A

104143160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116162-G-A

104143191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116192-C-T

104143254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116250-G-A

104143259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116255-T-C

104143294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116294-G-C

104143655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112116614-G-T

104144157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117025-C-T

104144158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117026-G-A

104144158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117026-G-C

104144291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117169-C-T

104144452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117382-C-T

104144583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117495-T-C

104144622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117533-T-C

104144708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117620-G-A

104144726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117639-C-T

104145207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117917-C-T

104145210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112117920-C-T

http://identifiers.org/hco/14/GRCh38#104145394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112118084-C-A

104145472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112118150-T-G

104145934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112118596-T-G

104145939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112118601-C-T

104146146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112118743-A-G

104146666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112119230-C-T

104146808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112119348-G-A

104146968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112119575-C-G

http://identifiers.org/hco/14/GRCh38#104147307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112120022-C-A

104147718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120295-C-T

104147831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120394-C-T

104147832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120395-G-A

104147832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120395-G-T

http://identifiers.org/hco/14/GRCh38#104148144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112120610-C-A

104148144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120610-C-T

104148149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120615-G-C

104148458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112120913-C-T

104148931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112121374-G-A

104149115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112121481-G-A

104149275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112121614-G-C

104149542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112121852-G-A

104149627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112121884-A-G

104149902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122136-G-A

104150110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122246-C-T

104150482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112122521-G-A

104150482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112122521-G-C

104150482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112122521-G-T

104150708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122716-A-G

104150718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122726-G-C

104150724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122732-G-C

http://identifiers.org/hco/14/GRCh38#104150758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112122766-C-A

104150758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122766-C-G

104150758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122766-C-T

104150854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122850-G-A

104150854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112122850-G-T

104151388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123206-G-A

104151396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123214-C-G

104151396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123214-C-T

104151658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123366-G-T

http://identifiers.org/hco/14/GRCh38#104151661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112123369-C-A

http://identifiers.org/hco/14/GRCh38#104151916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112123615-A-C

104151916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123615-A-G

104151916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123615-A-T

http://identifiers.org/hco/14/GRCh38#104151933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112123622-A-C

104151933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112123622-A-T

104152087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 112123754-G-A

104152161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112123828-C-G

104152183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112123850-G-A

104152222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112123883-A-G

104152332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112123978-T-C

104152484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112124125-G-T

http://identifiers.org/hco/14/GRCh38#104152547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112124180-C-A

104152547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112124180-C-T

http://identifiers.org/hco/14/GRCh38#104152560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112124193-C-A

104152560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112124193-C-G

104152560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112124193-C-T

104153863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112125882-G-A

104153863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112125882-G-C

104153864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112125883-G-A

104153866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112125885-T-G

104153970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112126007-A-G

104154464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112126415-C-T

104154521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112126469-C-T

104154522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112126470-G-A

104154522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112126470-G-T

104154541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112126491-G-A

104154902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112127263-T-C

104155018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112127561-C-T

104155473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112127926-C-G

http://identifiers.org/hco/14/GRCh38#104155604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112128074-C-A

104155797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128272-C-T

104155892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128343-G-A

104155957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128387-G-T

104156078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128470-C-T

104156112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128503-A-G

104156236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128615-G-A

104156377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112128728-G-A

http://identifiers.org/hco/14/GRCh38#104156739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112129000-C-A

104156943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129126-G-A

104156985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129173-G-A

104157586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129667-T-C

104157587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129668-G-C

104157608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129692-T-C

104157732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129764-A-G

http://identifiers.org/hco/14/GRCh38#104157733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112129765-C-A

104157733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112129765-C-T

104158995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112130552-C-T

104159006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112130563-C-T

104159084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112130630-G-A

104159251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112130797-G-A

104159268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112130818-G-A

104159421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112130981-C-G

104159456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131010-G-C

104159475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131024-T-G

104159497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131049-A-G

104159740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131309-G-T

104159770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131339-G-A

104159787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131354-G-A

104159898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131423-C-T

104160020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131543-C-T

104160069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131577-C-G

http://identifiers.org/hco/14/GRCh38#104160321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112131816-A-C

104160324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112131819-C-T

104163996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112134283-T-C

104164298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112134561-T-G

104164304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112134567-G-A

104164363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112134596-C-T

104166700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135029-A-G

104166713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135042-A-G

104166713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135042-A-T

104166729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135062-T-C

104166729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135062-T-G

104166752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135093-G-T

http://identifiers.org/hco/14/GRCh38#104166823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112135173-C-A

104166823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135173-C-G

104166823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135173-C-T

http://identifiers.org/hco/14/GRCh38#104166825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112135175-C-A

104166827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135177-C-G

104166827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135177-C-T

104166907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112135250-G-A

104166907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112135250-G-T

http://identifiers.org/hco/14/GRCh38#104166934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112135277-C-A

104166934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112135277-C-T

104167066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135407-T-C

http://identifiers.org/hco/14/GRCh38#104167089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112135432-C-A

104167089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135432-C-G

104167089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135432-C-T

104167162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135481-G-A

104167162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135481-G-T

http://identifiers.org/hco/14/GRCh38#104167180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112135505-C-A

104167180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135505-C-G

104167180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135505-C-T

104167183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135508-G-A

104167183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135508-G-T

104167187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135512-A-G

104167269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135593-C-G

104167326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112135649-G-A

104169611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112137074-G-A

104169756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112137220-G-T

104170092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112137496-C-T

104170101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112137505-T-C

104170115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112137518-G-A

104170471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112137888-T-C

104170848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112138208-G-A

104170879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112138244-G-A

104171494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, undefined
orthologous variants: 112138790-T-C

104171653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112138933-C-T

104171692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112138972-G-A

104171692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112138972-G-T

104171806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112139088-G-A

104171806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112139088-G-T

104171822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112139104-C-T

http://identifiers.org/hco/14/GRCh38#104171839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112139121-C-A

104171839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112139121-C-T

http://identifiers.org/hco/14/GRCh38#104171905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112139187-C-A

104171905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112139187-C-G

104171905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112139187-C-T

104172039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139275-G-T

104172252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139462-C-T

104172266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139474-C-T

104172282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139490-G-A

104172282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139490-G-T

104172432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139607-G-A

104172432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139607-G-T

104172472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139649-T-C

104172472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139649-T-G

104172513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139691-A-G

104172535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139715-G-A

104172535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139715-G-T

http://identifiers.org/hco/14/GRCh38#104172562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112139758-C-A

104172562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139758-C-T

104172571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 112139771-C-T

104172660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112139860-T-G

104172693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139899-A-G

104172734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139932-G-T

104172739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139937-T-A

104172739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139937-T-C

http://identifiers.org/hco/14/GRCh38#104172742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112139942-C-A

104172742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139942-C-T

104172784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139974-T-C

104172796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139985-G-C

104172796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112139985-G-T

104172817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140002-G-A

104172817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140002-G-T

104172851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140035-G-A

104173062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112140257-C-T

104173128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112140323-C-G

104173128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112140323-C-T

104173134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112140329-C-T

104173194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112140389-G-A

104173442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112140647-G-A

104173442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112140647-G-T

104173595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140765-G-A

104173595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140765-G-C

104173595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140765-G-T

104173600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140773-T-A

104173641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140809-G-T

104173683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140845-A-G

104173683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112140845-A-T

104173762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112140925-G-A

104173830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112140993-C-T

104173892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141054-G-A

104173900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141061-G-C

104173938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141099-G-A

104173938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141099-G-T

104174078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141163-T-A

104174078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141163-T-C

104174175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112141235-T-C

http://identifiers.org/hco/14/GRCh38#104174196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112141256-C-A

104174196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112141256-C-T

http://identifiers.org/hco/14/GRCh38#104174207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112141267-C-A

104174207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112141267-C-T

http://identifiers.org/hco/14/GRCh38#104174217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112141277-C-A

104174217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112141277-C-T

http://identifiers.org/hco/14/GRCh38#104174363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112141423-C-A

104174399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141451-G-A

104174399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141451-G-T

104174429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141467-G-T

104174446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141484-G-A

104174446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141484-G-T

104174470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141493-C-T

104174664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141604-G-A

104174667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141607-G-A

104174667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141607-G-C

104174712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141648-C-T

104174799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141731-T-C

104174826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141766-G-A

104174831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141771-G-A

104174831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141771-G-C

104174831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141771-G-T

104174900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141832-G-T

104174901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141833-G-A

104174901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112141833-G-T

104175071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142009-T-C

104175071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142009-T-G

http://identifiers.org/hco/14/GRCh38#104175105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112142043-C-A

104175105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142043-C-T

104175155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142093-G-A

104175155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142093-G-T

104175314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142252-G-A

http://identifiers.org/hco/14/GRCh38#104175383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112142321-C-A

104175383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142321-C-G

104175383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142321-C-T

104175503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142441-A-G

http://identifiers.org/hco/14/GRCh38#104175513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112142451-C-A

104175513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142451-C-G

104175573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142508-G-A

104175573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142508-G-C

104175573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142508-G-T

104175712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142647-G-C

104175712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112142647-G-T

http://identifiers.org/hco/14/GRCh38#104175836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112142771-C-A

104175836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142771-C-G

104175836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142771-C-T

104175854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142789-G-A

104175854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142789-G-T

http://identifiers.org/hco/14/GRCh38#104175989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112142924-C-A

104175989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142924-C-G

104175989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112142924-C-T

104176098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143048-A-G

http://identifiers.org/hco/14/GRCh38#104176124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143074-C-A

104176124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143074-C-T

http://identifiers.org/hco/14/GRCh38#104176243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143193-C-A

http://identifiers.org/hco/14/GRCh38#104176285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143235-C-A

104176285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143235-C-G

104176285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143235-C-T

104176328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143278-G-T

http://identifiers.org/hco/14/GRCh38#104176396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143346-C-A

104176396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143346-C-T

104176412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143362-C-T

104176559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143503-T-C

104176589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143533-C-T

104176626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143570-G-A

104176626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143570-G-C

104176626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143570-G-T

104176640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143584-G-A

104176640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143584-G-T

104176700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143644-A-G

104176760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143704-T-C

http://identifiers.org/hco/14/GRCh38#104176781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143725-C-A

104176781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143725-C-T

http://identifiers.org/hco/14/GRCh38#104176801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143745-C-A

104176801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112143745-C-T

104176886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143830-G-A

104176886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143830-G-C

104176886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143830-G-T

http://identifiers.org/hco/14/GRCh38#104176895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112143839-C-A

104176895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112143839-C-T

104177070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144008-G-T

http://identifiers.org/hco/14/GRCh38#104177071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144009-C-A

104177071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144009-C-G

104177071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144009-C-T

104177072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144010-A-G

104177072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144010-A-T

http://identifiers.org/hco/14/GRCh38#104177078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144016-C-A

104177078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144016-C-G

104177078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144016-C-T

104177151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144089-C-T

104177210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144148-C-T

104177291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144229-T-A

104177310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144248-T-A

104177310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144248-T-G

104177346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144283-G-A

104177346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144283-G-T

104177357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144292-G-A

104177357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144292-G-T

http://identifiers.org/hco/14/GRCh38#104177375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144310-C-A

104177375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144310-C-T

104177379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144314-G-A

104177379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144314-G-T

http://identifiers.org/hco/14/GRCh38#104177528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144463-C-A

104177528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144463-C-T

104177543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144478-G-A

104177543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144478-G-T

http://identifiers.org/hco/14/GRCh38#104177558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144493-C-A

104177558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144493-C-T

104177601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144536-A-G

104177601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112144536-A-T

104177609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144544-G-A

104177609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144544-G-T

104177645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144580-A-G

http://identifiers.org/hco/14/GRCh38#104177717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144652-C-A

104177717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144652-C-G

104177717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144652-C-T

104177738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144673-T-A

104177738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144673-T-C

104177738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144673-T-G

http://identifiers.org/hco/14/GRCh38#104177750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144685-C-A

104177750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144685-C-T

http://identifiers.org/hco/14/GRCh38#104177765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144700-C-A

104177765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144700-C-T

http://identifiers.org/hco/14/GRCh38#104177801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144736-C-A

104177801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous_variant, undefined
orthologous variants: 112144736-C-T

http://identifiers.org/hco/14/GRCh38#104177813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144748-C-A

104177813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144748-C-G

104177813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112144748-C-T

104177901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144836-G-T

104177904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144840-T-C

104177950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144856-G-C

104177950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144856-G-T

104177963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144869-C-G

104177963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144869-C-T

http://identifiers.org/hco/14/GRCh38#104177995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112144901-C-A

104177995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144901-C-T

104177996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144902-A-G

104178001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144912-G-C

104178035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144949-G-A

104178035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112144949-G-T

104178359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145382-T-C

http://identifiers.org/hco/14/GRCh38#104178414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145453-C-A

104178414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145453-C-T

http://identifiers.org/hco/14/GRCh38#104178425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145464-A-C

104178425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145464-A-G

104178425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145464-A-T

http://identifiers.org/hco/14/GRCh38#104178468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145501-C-A

104178468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145501-C-T

http://identifiers.org/hco/14/GRCh38#104178575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145602-C-A

104178575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112145602-C-T

http://identifiers.org/hco/14/GRCh38#104178623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145650-C-A

104178623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112145650-C-G

104178623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112145650-C-T

http://identifiers.org/hco/14/GRCh38#104178677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145704-C-A

104178677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112145704-C-G

104178677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112145704-C-T

104178710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112145737-G-A

104178710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112145737-G-T

104178771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145791-G-A

104178771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145791-G-T

104178829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145847-G-A

104178829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145847-G-C

104178829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145847-G-T

http://identifiers.org/hco/14/GRCh38#104178904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112145925-C-A

104178904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145925-C-G

104178904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145925-C-T

104178905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145926-G-A

104178905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145926-G-C

104178905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145926-G-T

104178921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112145944-C-T

http://identifiers.org/hco/14/GRCh38#104179087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112146069-C-A

104179087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146069-C-T

104179092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146080-T-C

104179092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146080-T-G

104179178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146160-T-C

104179218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146208-G-A

104179218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146208-G-C

104179218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146208-G-T

104179269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112146262-G-A

104179269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: 112146262-G-T

http://identifiers.org/hco/14/GRCh38#104179319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112146312-C-A

104179379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112146372-G-A

104179379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112146372-G-T

http://identifiers.org/hco/14/GRCh38#104179410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112146434-C-A

104179410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146434-C-T

104179478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146768-T-C

104179480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146770-G-A

104179480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146770-G-C

104179480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146770-G-T

http://identifiers.org/hco/14/GRCh38#104179528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112146819-C-A

104179528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146819-C-G

104179528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146819-C-T

104179530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146821-G-A

104179530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146821-G-C

104179532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146823-G-A

104179532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146823-G-T

104179567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146857-G-A

104179567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146857-G-C

104179567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146857-G-T

104179568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146858-G-T

http://identifiers.org/hco/14/GRCh38#104179570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112146860-C-A

104179570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146860-C-G

104179570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146860-C-T

104179597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: intron variant
orthologous variants: 112146873-T-C

104179757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: synonymous variant
orthologous variants: 112147033-T-C

104179812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147088-A-G

104179812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147088-A-T

http://identifiers.org/hco/14/GRCh38#104179818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147094-C-A

104179818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147094-C-T

http://identifiers.org/hco/14/GRCh38#104179825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147104-C-A

104179825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147104-C-G

104179825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147104-C-T

104179885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147163-T-C

104179885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147163-T-G

104179981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147247-G-A

104179981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147247-G-T

http://identifiers.org/hco/14/GRCh38#104180000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147266-A-C

104180000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147266-A-G

104180000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147266-A-T

104180046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147313-T-C

104180114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147390-G-C

104180114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147390-G-T

104180116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147392-G-A

104180116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147392-G-C

104180116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147392-G-T

http://identifiers.org/hco/14/GRCh38#104180133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147408-C-A

104180133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147408-C-T

104180201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147466-G-T

104180297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147542-G-A

104180297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147542-G-T

104180347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147592-G-A

104180347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147592-G-T

http://identifiers.org/hco/14/GRCh38#104180376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147623-A-C

http://identifiers.org/hco/14/GRCh38#104180377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147624-A-C

104180385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147632-T-C

104180385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147632-T-G

104180408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147664-G-A

104180408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147664-G-C

104180408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147664-G-T

http://identifiers.org/hco/14/GRCh38#104180473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147732-A-C

104180473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147732-A-G

104180473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147732-A-T

http://identifiers.org/hco/14/GRCh38#104180474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147733-C-A

104180478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147737-A-G

http://identifiers.org/hco/14/GRCh38#104180479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147738-C-A

104180479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147738-C-G

http://identifiers.org/hco/14/GRCh38#104180483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147742-C-A

http://identifiers.org/hco/14/GRCh38#104180672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112147958-C-A

104180672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112147958-C-T

104180720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112148007-C-T

http://identifiers.org/hco/14/GRCh38#104180749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112148036-C-A

104180749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112148036-C-G

104180749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20226
most severe consequence: 3 prime UTR variant
orthologous variants: 112148036-C-T