36871848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29480841-C-G

36871848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29480841-C-T

36871912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_donor_variant
orthologous variants: 29480888-G-C

36871912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_donor_variant
orthologous variants: 29480888-G-T

36871944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29480908-C-G

36872008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29480969-A-G

36872071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29481025-G-A

36872071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29481025-G-T

36872235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29481149-T-A

36872235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29481149-T-C

36874507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29482677-A-G

36874521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29482691-A-T

http://identifiers.org/hco/6/GRCh38#36874583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29482737-C-A

36874583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29482737-C-T

http://identifiers.org/hco/6/GRCh38#36874589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29482743-C-A

36874589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29482743-C-T

http://identifiers.org/hco/6/GRCh38#36874601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29482755-C-A

36874688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29482816-G-A

36874734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 29482863-G-A

36874734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 29482863-G-C

36874793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29482917-G-A

36874793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29482917-G-T

36874796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29482920-T-G

36874798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29482924-T-C

36874835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29482960-A-G

36874835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29482960-A-T

36874865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29482996-T-C

36874977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29483105-G-A

36874977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29483105-G-T

http://identifiers.org/hco/6/GRCh38#36874990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29483118-A-C

36874990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29483118-A-G

http://identifiers.org/hco/6/GRCh38#36875017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29483131-C-A

36875017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29483131-C-T

36875034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29483147-G-T

36875330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29483402-G-T

http://identifiers.org/hco/6/GRCh38#36885781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29487724-C-A

36885781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487724-C-G

36885781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487724-C-T

36885824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487769-T-A

36885824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487769-T-C

36885824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487769-T-G

http://identifiers.org/hco/6/GRCh38#36885827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29487772-C-A

36885827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487772-C-T

36885839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487789-G-A

36885839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29487789-G-T

36886046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29487994-G-A

36886046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29487994-G-T

36886280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29488167-C-T

36886460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29488333-G-C

36886460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29488333-G-T

36886464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29488337-A-G

36887038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29490305-C-T

36887069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29490334-C-T

36887741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491062-A-G

36887758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491079-A-T

36887980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491252-C-T

36888079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491415-A-G

36888212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491570-A-G

36888264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491619-G-A

36888353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491708-C-T

36888370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491725-G-A

36888444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29491789-C-T

36889180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29492941-A-G

36889208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29492963-T-C

http://identifiers.org/hco/6/GRCh38#36889247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29493000-C-A

36889247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29493000-C-T

http://identifiers.org/hco/6/GRCh38#36889582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29493286-C-A

36889676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29493351-G-T

36890345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29494169-G-A

36890345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29494169-G-C

36891686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29494892-C-T

36892170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29495899-C-T

36892215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29495926-T-G

36892635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29496213-A-G

http://identifiers.org/hco/6/GRCh38#36892832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29496898-C-A

36892832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 29496898-C-T

36899230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29500833-G-A

36899230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29500833-G-T

36899252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29500861-C-T

http://identifiers.org/hco/6/GRCh38#36899278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29500887-A-C

36899278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29500887-A-G

36899353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29500957-A-G

36899483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29501091-A-G

36899685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29501280-A-G

36899772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29501362-T-C

36902021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29501456-G-T

http://identifiers.org/hco/6/GRCh38#36902088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29501526-C-A

36902088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29501526-C-T

http://identifiers.org/hco/6/GRCh38#36902121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29501557-C-A

36902121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29501557-C-G

36902121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29501557-C-T

36902214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29501645-C-T

36902292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29501723-T-C

36902292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29501723-T-G

36902323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 29501754-C-T

36902332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 29501763-A-G

http://identifiers.org/hco/6/GRCh38#36902431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29501862-C-A

36902431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense variant
orthologous variants: 29501862-C-T

36902511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29502074-G-A

36902511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29502074-G-T

36902972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29502419-G-A

http://identifiers.org/hco/6/GRCh38#36903133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29502529-C-A

36903273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29502708-G-A

36903735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29503193-T-C

36906672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29504494-G-A

36906771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29504567-A-G

36911626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29510400-T-A

36911726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29510510-C-T

36911887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29510592-T-C

http://identifiers.org/hco/6/GRCh38#36911908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29510600-A-C

36911908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29510600-A-T

36911971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29510646-A-G

36912016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29510688-C-T

36912554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29511415-A-G

36912809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29511630-T-C

36912885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29511699-A-G

36912946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29511808-T-C

36913344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512409-G-C

36913409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512487-C-T

36913435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512531-T-G

36913550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512650-G-A

36913562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512661-A-G

36913580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512680-G-A

36913590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512690-C-T

36913764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512833-T-C

36914196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29512900-T-C

36914196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron_variant, undefined
orthologous variants: 29512900-T-G

36914217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512919-G-T

36914241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29512943-G-T

36914420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: synonymous variant
orthologous variants: 29513120-T-C

36914453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29513154-T-A

36914467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29513164-G-A

36914517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29513216-C-T

36914563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense variant
orthologous variants: 29513258-C-T

36914570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense_variant, undefined
orthologous variants: 29513265-T-C

36914570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense_variant, undefined
orthologous variants: 29513265-T-G

36914589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: synonymous_variant, undefined
orthologous variants: 29513284-T-C

36914628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: synonymous_variant, undefined
orthologous variants: 29513323-T-C

36914640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: synonymous variant
orthologous variants: 29513335-C-T

36914763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29513431-G-A

36915994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29514654-T-C

36916361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29515455-T-C

http://identifiers.org/hco/6/GRCh38#36916413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29515502-A-C

36916419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29515508-T-C

http://identifiers.org/hco/6/GRCh38#36916433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29515522-A-C

36916433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29515522-A-T

http://identifiers.org/hco/6/GRCh38#36916641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29515732-C-A

36916641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29515732-C-G

36917085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29515960-G-A

36917228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516042-T-G

36917252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516066-A-G

36917257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516070-G-A

36917257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516070-G-T

36917262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516075-A-T

36917408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516171-C-T

36917618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516363-G-A

36917657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516398-T-C

36917666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516407-G-A

36917678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516411-G-A

36917764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516482-C-T

36917887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516606-A-G

http://identifiers.org/hco/6/GRCh38#36917919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29516644-C-A

36917919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516644-C-G

36917919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516644-C-T

36917946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516662-T-C

36917946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516662-T-G

36917994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516709-G-T

36918065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516779-G-A

36918069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516783-T-C

36918074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29516788-A-G

36919559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29517586-T-C

36919607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: synonymous variant
orthologous variants: 29517645-T-C

http://identifiers.org/hco/6/GRCh38#36919729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29517767-C-A

36919986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29517970-C-T

36920005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29517989-G-A

36920270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29518222-T-G

36920690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29518562-G-A

36920916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29518755-G-A

36921150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29518909-C-T

36921455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29519149-A-G

36923334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29520317-A-G

36923334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: intron variant
orthologous variants: 29520317-A-T

36923394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense variant
orthologous variants: 29520377-G-A

36923414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: synonymous variant
orthologous variants: 29520397-C-T

36923435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: missense variant
orthologous variants: 29520418-A-T

36923478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520446-G-A

36923478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520446-G-C

36923497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520469-G-T

http://identifiers.org/hco/6/GRCh38#36923591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520558-C-A

36923594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520561-G-T

http://identifiers.org/hco/6/GRCh38#36923614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520581-C-A

36923614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520581-C-G

http://identifiers.org/hco/6/GRCh38#36923615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520582-C-A

36923615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520582-C-G

36923615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520582-C-T

36923646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520611-G-T

36923657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520623-G-A

36923748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520682-G-C

36923748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520682-G-T

http://identifiers.org/hco/6/GRCh38#36923774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520705-C-A

36923774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520705-C-T

http://identifiers.org/hco/6/GRCh38#36923775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520706-C-A

36923775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520706-C-G

36923782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520713-G-A

36923782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520713-G-T

36923802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520742-G-A

36923802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520742-G-T

http://identifiers.org/hco/6/GRCh38#36923880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520790-C-A

http://identifiers.org/hco/6/GRCh38#36923881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520791-A-C

36923898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520811-G-T

36923928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520838-G-A

http://identifiers.org/hco/6/GRCh38#36923973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29520900-C-A

36923973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520900-C-G

36923973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29520900-C-T

36924082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521071-G-A

36924082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521071-G-T

36924120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521218-T-C

36924356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521472-G-A

36924356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521472-G-T

36924443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521559-G-T

http://identifiers.org/hco/6/GRCh38#36924446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29521562-C-A

36924451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521567-G-T

36924708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29521919-G-T

http://identifiers.org/hco/6/GRCh38#36924715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29521925-C-A

36924818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522009-G-T

36924982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522188-G-T

36925047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522240-A-G

36925126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522302-A-G

36925128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522304-A-G

36925190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522366-G-A

http://identifiers.org/hco/6/GRCh38#36925421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29522558-A-C

36925421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522558-A-G

36925525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522654-T-C

36925529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522658-A-G

http://identifiers.org/hco/6/GRCh38#36925731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29522764-C-A

36925731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522764-C-T

http://identifiers.org/hco/6/GRCh38#36925758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29522777-C-A

36925777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522796-A-G

http://identifiers.org/hco/6/GRCh38#36925829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29522833-C-A

36925844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522848-G-A

36925844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522848-G-T

36925847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522851-T-C

36925943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522924-C-G

36925943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29522924-C-T

http://identifiers.org/hco/6/GRCh38#36925994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29522971-C-A

http://identifiers.org/hco/6/GRCh38#36926102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29523055-C-A

http://identifiers.org/hco/6/GRCh38#36926144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29523096-C-A

36926144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523096-C-T

36926169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523120-A-G

36926696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523424-T-A

36926803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523517-G-A

36926803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523517-G-T

36926824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523531-T-C

36926853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523550-C-T

36926854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523551-A-G

36926886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523584-T-C

36926899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523598-C-G

36926899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523598-C-T

36926953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29523650-C-T

http://identifiers.org/hco/6/GRCh38#36927322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29523981-C-A

36927853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524224-T-C

36928017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524384-T-C

36928078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524443-C-T

http://identifiers.org/hco/6/GRCh38#36928083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29524448-C-A

http://identifiers.org/hco/6/GRCh38#36928118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29524481-C-A

http://identifiers.org/hco/6/GRCh38#36928187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29524514-C-A

36928308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524634-A-G

http://identifiers.org/hco/6/GRCh38#36928418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29524732-C-A

36928418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524732-C-T

http://identifiers.org/hco/6/GRCh38#36928458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29524762-C-A

36928458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524762-C-T

36928581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524853-G-A

36928581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524853-G-T

http://identifiers.org/hco/6/GRCh38#36928639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29524912-C-A

36928639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29524912-C-T

36928786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29525027-G-A

http://identifiers.org/hco/6/GRCh38#36928812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29525053-C-A

36928812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29525053-C-T

http://identifiers.org/hco/6/GRCh38#36928846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29525068-C-A

36928895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21114
most severe consequence: 3 prime UTR variant
orthologous variants: 29525106-G-A