http://identifiers.org/hco/12/GRCh38#122983539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124256814-C-A

122983539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256814-C-G

122983573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256834-G-A

122983573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256834-G-T

122983665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256920-T-A

122983665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256920-T-C

122983666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256921-G-C

122983666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124256921-G-T

122983768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257058-T-G

122983851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257141-G-T

122983973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257266-T-A

122983973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257266-T-C

122984025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257312-G-A

122984222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257494-G-A

122984357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257617-G-A

122984357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257617-G-C

122984357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257617-G-T

122984497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257763-G-A

http://identifiers.org/hco/12/GRCh38#122984636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124257902-C-A

122984636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 124257902-C-T

122984680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124257944-C-T

122984760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 124258021-T-C

122984792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258047-G-A

122984792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258047-G-T

http://identifiers.org/hco/12/GRCh38#122984991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124258196-C-A

122984991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258196-C-T

122985168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258326-C-T

http://identifiers.org/hco/12/GRCh38#122985250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124258405-C-A

122985250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258405-C-G

122985250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258405-C-T

122985292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258477-G-A

122985293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258478-G-T

122985316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258503-G-T

122985393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258692-T-G

122985404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258703-A-G

122985611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258913-G-A

122985616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258918-A-G

122985640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258940-T-A

122985640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258940-T-G

http://identifiers.org/hco/12/GRCh38#122985667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124258952-C-A

122985667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258952-C-T

122985701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124258986-C-T

122985777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259062-T-C

122985777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259062-T-G

122985803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259088-C-G

122985803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259088-C-T

http://identifiers.org/hco/12/GRCh38#122985849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259132-C-A

122985849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259132-C-G

122985849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259132-C-T

122985937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259217-C-T

122986010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259310-G-A

122986010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259310-G-C

122986010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259310-G-T

http://identifiers.org/hco/12/GRCh38#122986018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259317-C-A

122986018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259317-C-G

122986018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 3 prime UTR variant
orthologous variants: 124259317-C-T

http://identifiers.org/hco/12/GRCh38#122986038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259337-C-A

122986038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124259337-C-T

122986042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259341-G-A

122986075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259374-G-A

122986075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259374-G-C

122986075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259374-G-T

122986077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124259376-G-A

122986077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124259376-G-T

http://identifiers.org/hco/12/GRCh38#122986276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259575-C-A

122986276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259575-C-G

122986276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259575-C-T

122986345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259644-G-A

122986345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124259644-G-T

http://identifiers.org/hco/12/GRCh38#122986425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259720-C-A

122986425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124259720-C-G

122986425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124259720-C-T

http://identifiers.org/hco/12/GRCh38#122986442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259737-C-A

http://identifiers.org/hco/12/GRCh38#122986520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259815-C-A

122986520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124259815-C-T

122986538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124259833-A-G

http://identifiers.org/hco/12/GRCh38#122986588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124259884-C-A

122986597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124259889-T-C

122986742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124260032-C-T

122986781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124260071-G-A

122986840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260140-G-A

122986840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260140-G-C

122986840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260140-G-T

http://identifiers.org/hco/12/GRCh38#122986861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124260165-C-A

122986861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260165-C-T

122986873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260195-T-A

122986873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260195-T-C

122986873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260195-T-G

http://identifiers.org/hco/12/GRCh38#122986897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124260225-C-A

122986897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260225-C-T

122987229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260599-C-T

122987319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124260671-G-A

122987461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124260811-C-G

122987718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261159-C-T

http://identifiers.org/hco/12/GRCh38#122987836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124261239-C-A

122987836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124261239-C-T

122987964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261374-G-A

122987964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261374-G-T

http://identifiers.org/hco/12/GRCh38#122987989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124261404-C-A

122987989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261404-C-G

122987989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261404-C-T

http://identifiers.org/hco/12/GRCh38#122988146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124261526-C-A

122988179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261555-G-A

122988179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261555-G-T

122988188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261564-T-C

122988270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124261642-C-G

122988378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261745-G-A

122988378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261745-G-T

http://identifiers.org/hco/12/GRCh38#122988393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124261761-C-A

122988393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261761-C-G

122988393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261761-C-T

http://identifiers.org/hco/12/GRCh38#122988406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124261771-C-A

122988406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261771-C-T

122988433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261798-G-A

http://identifiers.org/hco/12/GRCh38#122988437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124261805-C-A

122988455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261822-T-C

122988466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261833-T-C

122988494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261869-A-G

122988613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261937-G-A

122988613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261937-G-T

122988664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124261973-T-C

http://identifiers.org/hco/12/GRCh38#122988745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262023-C-A

122988745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124262023-C-G

122988745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124262023-C-T

http://identifiers.org/hco/12/GRCh38#122988796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262074-C-A

122988796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124262074-C-G

122988796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124262074-C-T

122988915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262191-A-G

http://identifiers.org/hco/12/GRCh38#122988917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262193-A-C

122988917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262193-A-G

http://identifiers.org/hco/12/GRCh38#122988942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262218-C-A

http://identifiers.org/hco/12/GRCh38#122989000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262282-C-A

http://identifiers.org/hco/12/GRCh38#122989029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262307-C-A

122989029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262307-C-T

http://identifiers.org/hco/12/GRCh38#122989330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262544-A-C

122989515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262666-G-C

http://identifiers.org/hco/12/GRCh38#122989670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124262752-C-A

122989670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262752-C-T

122989690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262772-T-G

122989770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262847-A-G

122989770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124262847-A-T

122989985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263061-G-A

122989985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263061-G-C

122989985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263061-G-T

122990030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263109-G-T

122990376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263281-C-T

http://identifiers.org/hco/12/GRCh38#122990408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124263303-C-A

122990408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263303-C-T

http://identifiers.org/hco/12/GRCh38#122990417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124263312-C-A

122990443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263333-G-A

122990443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263333-G-C

122990443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263333-G-T

122990681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124263498-G-A

http://identifiers.org/hco/12/GRCh38#122990754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124263571-C-A

http://identifiers.org/hco/12/GRCh38#122990767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124263587-A-C

122990818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263625-G-C

122990818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263625-G-T

http://identifiers.org/hco/12/GRCh38#122990823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124263630-C-A

122990823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263630-C-T

122991064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263819-C-T

http://identifiers.org/hco/12/GRCh38#122991119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124263853-C-A

122991119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263853-C-T

122991180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263887-C-T

122991289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124263974-G-C

122991326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264001-C-G

122991439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264097-C-T

122991692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, missense_variant
orthologous variants: 124264361-T-C

http://identifiers.org/hco/12/GRCh38#122991705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124264367-C-A

122991705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124264367-C-T

122991851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124264520-G-A

122991851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, missense_variant
orthologous variants: 124264520-G-T

122992004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264672-G-C

122992004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264672-G-T

122992024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264694-G-A

122992024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264694-G-C

122992024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264694-G-T

122992036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264706-G-A

122992036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264706-G-T

122992295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264981-T-C

122992295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124264981-T-G

122992322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265011-G-A

http://identifiers.org/hco/12/GRCh38#122992328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124265032-A-C

http://identifiers.org/hco/12/GRCh38#122992349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124265088-C-A

122992349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265088-C-T

122992398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265144-C-G

122992436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265209-G-A

122992436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265209-G-C

http://identifiers.org/hco/12/GRCh38#122992459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124265220-C-A

122992459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265220-C-G

122992459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265220-C-T

http://identifiers.org/hco/12/GRCh38#122992560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124265301-C-A

122992560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124265301-C-T

122992650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124265391-G-A

122992651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, missense_variant
orthologous variants: 124265392-G-A

122992656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124265397-C-T

122992678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265419-G-T

http://identifiers.org/hco/12/GRCh38#122992712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124265442-A-C

122992712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265442-A-G

122992712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265442-A-T

122992727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265452-G-A

122992727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265452-G-T

122992790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265485-G-A

122992790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265485-G-C

122992790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124265485-G-T

122994493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266413-G-A

122994595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266483-A-G

122994661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266550-G-A

http://identifiers.org/hco/12/GRCh38#122994665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266554-C-A

122994665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266554-C-G

122994665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266554-C-T

122994674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266563-G-A

122994674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266563-G-C

122994674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266563-G-T

122994717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266595-T-C

122994717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266595-T-G

http://identifiers.org/hco/12/GRCh38#122994748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266624-C-A

122994748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266624-C-T

122994791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266656-G-A

http://identifiers.org/hco/12/GRCh38#122994844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266709-C-A

http://identifiers.org/hco/12/GRCh38#122994973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266838-A-C

122994973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124266838-A-G

122994976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124266841-G-A

122994976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124266841-G-T

http://identifiers.org/hco/12/GRCh38#122994988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266871-C-A

http://identifiers.org/hco/12/GRCh38#122994994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266898-A-C

122995014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266926-G-A

122995014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266926-G-T

http://identifiers.org/hco/12/GRCh38#122995069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124266982-C-A

122995069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124266982-C-G

122995384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267222-C-T

122995487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124267325-G-A

122995487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124267325-G-T

http://identifiers.org/hco/12/GRCh38#122995579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124267396-C-A

122995579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124267396-C-T

122995586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124267403-G-A

122995586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124267403-G-T

http://identifiers.org/hco/12/GRCh38#122995609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124267414-C-A

122995609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense variant
orthologous variants: 124267414-C-T

122995658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 124267463-G-A

122995658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 124267463-G-T

122995890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267713-G-A

122995890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267713-G-C

122995959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267786-T-A

122996001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267816-T-G

122996013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267828-C-G

122996050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124267864-C-G

http://identifiers.org/hco/12/GRCh38#122996346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124268122-C-A

http://identifiers.org/hco/12/GRCh38#122996398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124268186-C-A

122996398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268186-C-G

122996398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268186-C-T

122996607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268419-C-T

122996639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268451-A-G

122996639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268451-A-T

http://identifiers.org/hco/12/GRCh38#122996662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124268488-C-A

122996662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268488-C-G

http://identifiers.org/hco/12/GRCh38#122997001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124268818-C-A

122997052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268864-G-A

122997052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268864-G-C

122997052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124268864-G-T

http://identifiers.org/hco/12/GRCh38#122997143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124268964-C-A

122997279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124269094-G-A

122997279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124269094-G-T

http://identifiers.org/hco/12/GRCh38#122997281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124269096-C-A

122997281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124269096-C-G

122997281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124269096-C-T

122997414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124269247-G-A

122997414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124269247-G-T

122997429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: synonymous variant
orthologous variants: 124269262-G-A

122997628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124269478-G-A

122997628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124269478-G-T

http://identifiers.org/hco/12/GRCh38#122997631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124269481-C-A

http://identifiers.org/hco/12/GRCh38#122997714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124269602-C-A

122997714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124269602-C-T

122998025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124269837-C-T

122998050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124269860-G-A

122999434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124270060-C-T

123000136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124270712-C-T

http://identifiers.org/hco/12/GRCh38#123000176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124270748-C-A

123000176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124270748-C-T

123000177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124270749-A-G

123000213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124270790-C-T

123000492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271052-G-C

123000617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271125-A-G

http://identifiers.org/hco/12/GRCh38#123000728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124271194-C-A

123000728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271194-C-T

http://identifiers.org/hco/12/GRCh38#123000845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124271298-C-A

123000845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124271298-C-T

123000916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271348-G-A

123000916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271348-G-T

123000956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271359-T-G

123000957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271360-G-T

123000963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271363-C-T

123000995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271396-G-A

123001148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124271522-G-A

123001170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271544-A-G

123001198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271572-G-A

123001198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271572-G-C

123001198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271572-G-T

http://identifiers.org/hco/12/GRCh38#123001271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124271616-C-A

123001271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271616-C-T

123001294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271632-G-T

123001460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271747-G-T

123001481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124271774-T-C

http://identifiers.org/hco/12/GRCh38#123003802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124272649-C-A

123004085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124272934-G-A

123004246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124273090-C-T

http://identifiers.org/hco/12/GRCh38#123004290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124273133-C-A

123004290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124273133-C-T

123004329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124273147-C-T

123004361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124273179-G-A

123004587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124273407-G-T

http://identifiers.org/hco/12/GRCh38#123004706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124273527-C-A

123004706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124273527-C-T

123005130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124274054-T-A

123005130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124274054-T-C

123005161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124274081-T-C

123005161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124274081-T-G

123005312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124274234-G-T

http://identifiers.org/hco/12/GRCh38#123005679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124274547-C-A

123005679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124274547-C-T

123005767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124274635-A-G

123007002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124275643-C-T

123007004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124275645-G-A

123007098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124275749-T-G

123007148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124275797-A-G

123007325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124275975-G-T

123007486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124276123-G-T

123007681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124276314-T-C

123007885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124276462-G-A

123007885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124276462-G-T

123008181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124276687-C-T

123008428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124276868-C-T

123008740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124277188-T-C

123008766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124277213-T-A

123008766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124277213-T-C

123008795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124277243-A-T

123009762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124278546-T-A

123009762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124278546-T-C

123009762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124278546-T-G

123010712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124279429-A-G

123010736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124279453-A-T

123012068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124279544-A-G

123012778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124280293-G-A

123013264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124281084-G-A

123013264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124281084-G-T

123013579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124281294-C-T

123013690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124281402-A-G

123013842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124281510-G-A

123013884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124281552-C-T

http://identifiers.org/hco/12/GRCh38#123014832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124282460-C-A

123014952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124282576-G-T

123023251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124283692-T-C

123023289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124283752-T-C

123023335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124283806-C-T

123023603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124284167-C-T

123023644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124284208-C-T

123026878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124285372-T-C

123027129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124285620-C-T

123027525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124285944-T-C

123027658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286067-T-G

123027665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286082-G-A

123027680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286118-A-G

123027700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286144-G-C

123027721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286164-T-A

123027785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286234-C-G

123027785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286234-C-T

123027797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286246-A-G

123027850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286298-G-T

123027868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286316-C-T

123028067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286481-G-A

123028155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286579-C-T

123028167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286589-C-T

123028247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124286660-C-G

123028944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124287236-G-A

123028944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124287236-G-C

123029043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124287362-G-A

123029201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124287550-G-A

http://identifiers.org/hco/12/GRCh38#123029422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124287803-C-A

123031827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124288598-C-T

123031877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124288647-G-A

123032526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124288852-G-A

123032798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124289122-C-T

http://identifiers.org/hco/12/GRCh38#123032919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124289243-A-C

123033099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124289547-C-T

123033390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124289790-G-A

123033411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124289805-G-C

123033705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124290050-A-G

123033764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124290117-G-A

123034053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124290231-G-A

123034175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124290317-T-A

http://identifiers.org/hco/12/GRCh38#123034258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124290373-C-A

123034318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124290434-G-A

123034318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124290434-G-C

123034318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124290434-G-T

123034451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124290541-G-T

123034597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124290691-G-A

http://identifiers.org/hco/12/GRCh38#123034703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124290833-C-A

123034754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124290880-G-T

123034816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124290931-T-C

123034945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124291065-T-C

123037782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124291508-T-C

123040936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296232-A-G

123041113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296399-T-C

123041306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296575-G-A

123041343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296603-G-T

http://identifiers.org/hco/12/GRCh38#123041353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124296612-C-A

123041387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296669-G-A

123041449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296765-T-C

123041520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124296828-A-T

http://identifiers.org/hco/12/GRCh38#123041823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124297104-C-A

123041840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297128-G-A

123042040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297323-G-A

123042040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297323-G-C

123042261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297507-G-A

123042368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297606-G-C

123042459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297697-T-C

123042700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124297926-C-G

123042804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298001-C-T

123042960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298101-T-G

123043186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298301-C-T

http://identifiers.org/hco/12/GRCh38#123043395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124298641-C-A

123043395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298641-C-T

123043549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298777-C-G

123043592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298808-T-C

123043617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298833-C-T

123043702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298880-C-T

123043778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298954-C-G

123043778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298954-C-T

http://identifiers.org/hco/12/GRCh38#123043798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124298974-C-A

123043798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124298974-C-T

123043996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124299146-C-G

123043996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124299146-C-T

123045025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124301120-T-G

123045292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124301350-C-G

http://identifiers.org/hco/12/GRCh38#123045704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124301745-C-A

123045866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124301863-G-A

123045868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124301865-C-T

123045881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124301876-C-G

123046816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124302629-C-T

123046897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124302708-T-C

123047640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124303514-C-T

http://identifiers.org/hco/12/GRCh38#123049282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124303729-A-C

123049282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124303729-A-T

123049396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124303870-C-T

123049704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304146-C-T

123049824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304231-G-A

123050237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304612-A-G

123050393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304675-C-T

123050480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304762-G-A

123050481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304763-A-G

123050504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304787-G-A

123050561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304844-G-A

123050696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124304964-G-A

123051166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124305484-T-C

123051168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124305486-G-C

123051279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124305580-C-G

123051972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124306366-G-A

123051972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124306366-G-T

123052027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124306477-C-T

123052045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124306494-G-T

123054725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124306782-T-C

http://identifiers.org/hco/12/GRCh38#123055347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124307040-C-A

http://identifiers.org/hco/12/GRCh38#123055492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124307408-C-A

123055671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124307587-C-T

http://identifiers.org/hco/12/GRCh38#123056865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124307800-C-A

http://identifiers.org/hco/12/GRCh38#123062507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124309691-C-A

http://identifiers.org/hco/12/GRCh38#123062622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124309810-A-C

123062751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124309938-T-G

123063551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124310802-C-T

123063571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124310822-T-C

123063639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124310867-C-T

123063662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124310886-G-A

123063696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124310904-A-T

123063956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124311117-C-G

123064165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124311274-C-G

123064167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124311276-G-A

123064181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124311291-C-T

123064275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124311378-C-G

123064833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312068-C-G

123064833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312068-C-T

123064837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312072-C-G

123064837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312072-C-T

123064841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312076-T-C

http://identifiers.org/hco/12/GRCh38#123064862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124312097-A-C

123064863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312098-G-A

123065090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312333-G-A

123065142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312380-G-A

123065142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312380-G-C

123065152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312390-G-A

http://identifiers.org/hco/12/GRCh38#123065232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124312442-A-C

http://identifiers.org/hco/12/GRCh38#123065243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124312453-A-C

123065304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312491-C-G

123065643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124312786-G-A

123065917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124313003-T-A

123066044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124313125-G-A

123066264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124313349-G-A

123066284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124313369-G-C

123068012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124315022-C-T

http://identifiers.org/hco/12/GRCh38#123068100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124315101-A-C

http://identifiers.org/hco/12/GRCh38#123068101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124315102-C-A

123069435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316084-G-A

http://identifiers.org/hco/12/GRCh38#123069578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124316180-A-C

123069799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316359-T-C

123069810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316370-A-T

123069834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316394-G-C

123069942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316494-T-G

123070150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316680-C-G

123070187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316717-G-A

123070254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316789-A-G

123070262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316797-C-G

123070262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316797-C-T

123070375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316850-C-T

123070380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316854-G-A

123070463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124316921-T-C

http://identifiers.org/hco/12/GRCh38#123071202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124317310-C-A

http://identifiers.org/hco/12/GRCh38#123071685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124318473-C-A

123071685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124318473-C-T

123071914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124318701-G-A

123071914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124318701-G-T

http://identifiers.org/hco/12/GRCh38#123071975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124318774-C-A

123071975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124318774-C-G

123072012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124318809-G-A

http://identifiers.org/hco/12/GRCh38#123072100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124318888-C-A

123072100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124318888-C-T

123072239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124319007-T-C

123072438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124319343-G-A

123072441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124319346-G-C

123072499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124319422-T-A

123073136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124320039-C-T

123073160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124320057-T-A

123073603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124320511-C-T

123073687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124320582-C-T

123073763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124320675-G-A

http://identifiers.org/hco/12/GRCh38#123073779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124320691-C-A

123073779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124320691-C-T

123074304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124321123-G-A

123074362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124321177-T-C

123074432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124321259-A-T

123074466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124321301-A-T

http://identifiers.org/hco/12/GRCh38#123075428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124322844-C-A

123075428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124322844-C-T

http://identifiers.org/hco/12/GRCh38#123075456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124322870-C-A

http://identifiers.org/hco/12/GRCh38#123075460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124322874-C-A

123075697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124323119-T-C

123075780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124323227-G-C

123075780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124323227-G-T

123075798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124323245-A-G

123075939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124323379-C-T

123076176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323606-G-C

123076176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323606-G-T

http://identifiers.org/hco/12/GRCh38#123076195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124323629-A-C

123076195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323629-A-G

http://identifiers.org/hco/12/GRCh38#123076210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124323643-C-A

123076210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323643-C-T

123076231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323664-T-C

123076301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323712-C-T

123076364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323773-G-A

123076518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323903-C-T

123076549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323941-G-A

123076549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323941-G-C

123076551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124323945-C-T

123076693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124324066-A-G

123077095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124324424-A-T

http://identifiers.org/hco/12/GRCh38#123077332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124324595-C-A

123077955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124325162-C-T

http://identifiers.org/hco/12/GRCh38#123078456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124325635-C-A

123078456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124325635-C-T

123078517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124325699-C-T

123078811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124325954-C-T

123078921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326061-C-T

123079054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326194-C-T

123079093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326233-T-C

123079731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326506-T-A

123079731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326506-T-C

123079923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326701-C-T

123079998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326761-C-T

123080011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326774-T-C

123080128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124326897-A-G

123080506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124327071-G-A

http://identifiers.org/hco/12/GRCh38#123080871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124327354-C-A

http://identifiers.org/hco/12/GRCh38#123080909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124327392-C-A

123081037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124327504-T-C

123081083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124327549-A-G

123081083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124327549-A-T

123081115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124327569-T-G

http://identifiers.org/hco/12/GRCh38#123081137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124327591-C-A

123081137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124327591-C-T

123081195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124327649-T-C

123081464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124327918-T-C

123081505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124327954-A-T

123081509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124327958-A-G

123081524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124327975-G-T

http://identifiers.org/hco/12/GRCh38#123081525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124327976-C-A

123081525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124327976-C-T

123081567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328019-G-T

123081599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328048-C-T

123081614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328063-A-G

http://identifiers.org/hco/12/GRCh38#123081640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124328089-A-C

123081640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328089-A-G

http://identifiers.org/hco/12/GRCh38#123081660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124328101-C-A

123081660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328101-C-G

123081660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328101-C-T

123081703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328131-G-A

123081703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328131-G-T

http://identifiers.org/hco/12/GRCh38#123081739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124328154-C-A

123081742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328157-G-T

123081832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328243-C-T

http://identifiers.org/hco/12/GRCh38#123081870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124328280-C-A

123081870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124328280-C-T

123082763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329174-T-C

123082798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124329210-A-G

123082831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124329239-C-T

http://identifiers.org/hco/12/GRCh38#123082876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124329284-C-A

http://identifiers.org/hco/12/GRCh38#123082945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124329348-C-A

123082950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124329353-T-C

123082962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329365-A-G

123082962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329365-A-T

123083070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329460-C-T

123083155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329571-C-T

123083188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329600-T-A

123083190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329602-T-A

123083190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329602-T-C

123083199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124329625-A-G

http://identifiers.org/hco/12/GRCh38#123083333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124329784-C-A

123083333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124329784-C-T

123083406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124329910-G-T

123083436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124329926-T-C

123083484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124329981-G-A

123083699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330318-G-A

123083699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330318-G-T

123083804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330413-C-T

123083914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330532-T-C

123083990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330608-G-A

123083990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330608-G-T

http://identifiers.org/hco/12/GRCh38#123084008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124330625-C-A

123084008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330625-C-T

http://identifiers.org/hco/12/GRCh38#123084017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124330632-C-A

123084098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330697-A-G

123084101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330700-G-A

123084101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330700-G-C

http://identifiers.org/hco/12/GRCh38#123084102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124330701-C-A

123084102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124330701-C-T

123084439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124331040-G-A

123084439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124331040-G-C

123084439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124331040-G-T

123084478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124331090-G-A

123084478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124331090-G-T

http://identifiers.org/hco/12/GRCh38#123084568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124331175-C-A

http://identifiers.org/hco/12/GRCh38#123084579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124331186-C-A

123084579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124331186-C-T

http://identifiers.org/hco/12/GRCh38#123084980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124331582-C-A

http://identifiers.org/hco/12/GRCh38#123085237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124331795-C-A

123085237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124331795-C-T

123085398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124331927-C-G

123085538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124332039-G-A

123085623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332107-C-T

123085633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332117-T-C

http://identifiers.org/hco/12/GRCh38#123085838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124332257-A-C

123085920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332316-C-T

123086040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332420-T-C

123086058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332440-G-A

123086058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332440-G-C

123086164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124332547-T-C

123086468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124332844-T-C

123086688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333094-T-C

123086696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333119-C-T

123086743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333166-T-C

123086743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333166-T-G

123087135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333528-T-C

123087155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333548-T-C

http://identifiers.org/hco/12/GRCh38#123087238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124333692-C-A

123087238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124333692-C-G

123087267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124333713-G-T

123087293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124333739-G-T

123087316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124333768-A-G

123087401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124333831-T-C

123087964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124333899-G-T

123088032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124333963-A-G

123088071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334002-A-G

123088212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334112-G-A

123088212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334112-G-T

123088217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334116-T-C

123088477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334340-G-T

123088514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334358-T-C

123088700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334534-T-C

123088713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334547-G-A

123088907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334736-C-T

123088945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334775-A-G

123089070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124334911-C-T

http://identifiers.org/hco/12/GRCh38#123089214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124335006-C-A

123089214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124335006-C-T

123089409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124335151-T-C

123089673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124335369-A-G

http://identifiers.org/hco/12/GRCh38#123089699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124335389-C-A

123089765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124335442-G-A

123089765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124335442-G-T

123089797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124335482-G-T

123089803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124335491-G-C

123089827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124335515-T-A

123090357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124336608-A-G

123090361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 124336612-G-A

http://identifiers.org/hco/12/GRCh38#123090364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#124336615-A-C

123091002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337293-A-G

http://identifiers.org/hco/12/GRCh38#123091069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124337356-C-A

123091069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337356-C-G

123091069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337356-C-T

123091244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337529-G-A

123091244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337529-G-C

123091391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337676-T-C

123091409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337694-C-G

123091458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337742-C-T

123091530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337806-G-A

123091530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337806-G-T

123091532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337810-G-A

123091532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337810-G-T

123091547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337826-T-C

123091549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337828-G-T

123091554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337835-G-T

http://identifiers.org/hco/12/GRCh38#123091605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124337880-C-A

123091605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337880-C-T

123091620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337902-G-T

123091706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337983-C-G

123091707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337984-T-C

123091707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124337984-T-G

123092004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338173-T-C

123092044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338209-A-G

123092092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338244-A-T

123092150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338299-G-A

123092150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338299-G-T

http://identifiers.org/hco/12/GRCh38#123092408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124338382-C-A

123092635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338608-C-T

http://identifiers.org/hco/12/GRCh38#123092648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124338615-C-A

123092648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338615-C-T

123092742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338707-C-T

http://identifiers.org/hco/12/GRCh38#123092820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124338771-C-A

123092820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124338771-C-T

http://identifiers.org/hco/12/GRCh38#123092830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124338781-C-A

123093114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124339057-G-C

123093415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124339275-T-C

123093489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124339495-C-T

123093915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124339945-G-T

123094762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124340794-G-A

123094867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124342336-T-G

123095018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124342494-T-C

123095406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124342866-C-G

123095449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124342908-A-G

123095479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343033-T-C

123095561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343109-C-T

123095563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343111-A-G

123095719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343263-C-T

123096201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343690-T-C

123096285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343786-G-A

123096337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124343832-C-T

123096772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124344221-G-T

123096826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124344256-C-T

123096902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124344336-G-A

123097340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124344430-G-A

123097766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124344828-G-A

123098081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124345135-C-G

123098081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124345135-C-T

123098923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124346012-G-A

123099455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124346436-G-C

123102630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124348849-T-A

123102630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124348849-T-C

123102906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 124349049-G-T

123103119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124349102-T-C

123103134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124349115-C-T

123103445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124349464-T-G

123103595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124349581-C-T

123103725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124349709-A-G

123106774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124351582-G-A

123106788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124351596-C-G

123107396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124352091-G-A

123107491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124352194-G-C

123107569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124352268-G-A

123107611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124352303-C-G

123107723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124352416-C-G

123108747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353400-C-T

123108760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353413-G-C

http://identifiers.org/hco/12/GRCh38#123108803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124353444-C-A

123108803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353444-C-T

123108938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353546-T-A

123109154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353706-T-C

123109155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353707-T-G

123109214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353766-T-C

123109215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353767-G-C

123109235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353788-C-T

123109529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124353924-A-G

123109612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354010-C-T

123109692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354089-T-A

123109695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354092-C-T

123109728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354129-G-A

123109790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354194-C-G

123110234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354261-G-A

123110285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354306-G-A

123110285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124354306-G-T

123110408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124354401-T-C

123110408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 124354401-T-G

http://identifiers.org/hco/12/GRCh38#123110451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124354443-A-C

123110501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124354494-G-A

123110501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124354494-G-T

123110593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124354622-G-T

123110618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124354648-G-A

123110618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124354648-G-T

123111047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124354984-G-A

123111160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124355660-C-T

123111613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124356130-G-A

123111866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124356431-C-T

123113129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124357277-A-G

123113154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124357302-T-C

123113956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124357770-T-G

123114071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124357993-A-G

123114620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124358511-G-A

123114751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124358570-T-C

http://identifiers.org/hco/12/GRCh38#123114762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124358578-A-C

http://identifiers.org/hco/12/GRCh38#123114959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124358736-C-A

123114959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124358736-C-T

123114989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124358766-G-A

123115078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124358922-C-T

123115406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124359271-C-T

123115946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124359788-C-T

123116155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124359980-T-C

123116562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124360355-T-C

123116745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124360580-C-G

http://identifiers.org/hco/12/GRCh38#123116822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124360665-A-C

123117107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124360908-C-G

123117173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124360976-A-G

123118585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124361876-C-T

123118918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362198-T-C

123118978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362285-G-A

123119008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362315-T-C

123119017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362324-G-A

123119017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362324-G-T

123119193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362475-T-A

123119444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124362638-G-A

123120465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124363879-G-C

123120518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124363923-C-T

123120522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124363927-C-T

123120696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124364085-A-T

123120741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124364127-G-A

123121121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124364515-C-T

123122528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124364977-G-A

123122915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124365375-T-C

123122921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124365381-A-G

123123001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124365452-T-C

123123079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124365528-A-G

123123273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124365699-A-G

123125571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124366543-G-A

123125648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124366609-G-A

123125648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124366609-G-T

http://identifiers.org/hco/12/GRCh38#123126243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124366846-C-A

123127068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124367649-C-T

123127239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124367807-C-T

123127367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124367919-G-A

123127495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124368047-T-G

123129635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: -C-T

123129734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: -C-T

123129824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: -C-T

123129852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: -T-C

123130157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124368760-A-G

123130637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124369171-G-A

123130652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124369186-C-T

123132076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370434-C-T

123132173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370534-C-T

123132292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370640-C-T

123132326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370671-C-G

123132429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370752-C-T

123132452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370772-C-T

123132602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370890-C-G

123132602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370890-C-T

123132633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124370915-T-C

123132870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124371066-A-T

123133034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124371216-A-T

123133042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124371224-C-T

123133305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124371441-G-A

123133444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124371567-C-T

123133462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124371585-T-C

123134432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124372516-G-A

123134444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124372528-G-A

123134510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124372579-G-A

123134519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124372594-G-A

123134576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124372666-C-G

123134735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124372811-C-T

123137201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124374689-T-C

123137280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124374761-C-T

123138410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124375668-T-C

123140029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124376883-G-A

123140135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124376982-G-T

123140686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124378124-G-T

123141369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124378766-C-T

123141421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124378800-G-A

123141456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124378834-G-C

123141637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124378969-G-A

123141637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124378969-G-C

http://identifiers.org/hco/12/GRCh38#123141816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124379106-C-A

123141816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124379106-C-T

123141861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124379151-C-G

123142046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124379327-G-T

http://identifiers.org/hco/12/GRCh38#123142331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124379612-C-A

123142331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124379612-C-G

123142761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124380042-C-T

123142763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124380044-T-A

123142859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124380146-T-C

123143464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124380569-T-G

123143496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, undefined
orthologous variants: 124380597-G-A

123143642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124380712-T-C

123143716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124380788-T-C

123143940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124380986-C-T

123143988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124381027-G-A

123145612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124383060-G-A

123146656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124383185-T-A

123147143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124383611-C-G

http://identifiers.org/hco/12/GRCh38#123147534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124383868-A-C

123147776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124384450-G-A

123148294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385177-C-T

123148367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385263-G-A

123148547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385447-G-A

123148776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385658-T-A

123148787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385671-G-A

http://identifiers.org/hco/12/GRCh38#123148845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124385724-C-A

123148845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385724-C-T

123148876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124385753-C-T

123149251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386078-G-C

123149288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386113-G-T

http://identifiers.org/hco/12/GRCh38#123149297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124386122-C-A

http://identifiers.org/hco/12/GRCh38#123149443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124386269-C-A

123149496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386318-T-C

http://identifiers.org/hco/12/GRCh38#123149543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124386330-C-A

123149575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386363-A-G

123149584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron_variant, undefined
orthologous variants: 124386372-A-G

123149606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386394-G-A

123149649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386439-T-A

123149756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386521-A-G

123149756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386521-A-T

123149800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124386550-T-C

123149800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124386550-T-G

123149917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124386642-G-A

123149917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 124386642-G-T

http://identifiers.org/hco/12/GRCh38#123149999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124386714-C-A

123150034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386754-G-A

123150034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386754-G-C

http://identifiers.org/hco/12/GRCh38#123150116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124386829-C-A

123150116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124386829-C-T

123150487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124387266-A-G

123150639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: intron variant
orthologous variants: 124387374-G-A

123151020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21044
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 124387759-G-A