31200267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149601900-G-A

31200267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149601900-G-T

31200510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149602062-T-C

31200959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149603139-C-T

31201891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149603985-T-C

31202454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149604703-C-G

31202591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149604832-G-A

31202884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149605074-G-A

http://identifiers.org/hco/13/GRCh38#31206128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149609546-A-C

31206128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149609546-A-G

31206201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149609613-C-T

31207001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149611348-C-T

31207046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149611391-G-A

http://identifiers.org/hco/13/GRCh38#31207066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149611410-C-A

31207323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149611612-C-T

31207444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149611724-G-A

31208243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149612026-A-G

31208843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149612710-C-T

31208916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149612774-G-T

http://identifiers.org/hco/13/GRCh38#31209500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149614031-C-A

31209500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614031-C-G

31209694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614181-G-A

31210094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614605-A-G

31210141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614664-T-C

http://identifiers.org/hco/13/GRCh38#31210169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149614692-A-C

31210339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614849-T-G

31210384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614895-C-G

31210446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149614958-C-G

31211759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616043-G-A

31211924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616199-T-C

31211940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616214-T-G

31211946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616220-C-G

31211946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616220-C-T

31211999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616273-T-C

31211999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616273-T-G

31212136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149616403-C-T

31212899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149617769-A-G

31213034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149617927-G-T

31213058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149617951-A-G

31213058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149617951-A-T

31213062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149617955-G-C

http://identifiers.org/hco/13/GRCh38#31213706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149618609-A-C

31213788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149618701-G-C

31213848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149618752-C-T

31213965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149618869-A-G

31213994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149618897-A-G

31214017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149618920-C-G

31214333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619159-G-T

31214357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619183-G-A

31214619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619431-T-C

31214660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619471-A-G

31214753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619546-A-T

31214788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619584-G-A

http://identifiers.org/hco/13/GRCh38#31215144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149619982-C-A

31215144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619982-C-T

31215151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149619989-A-G

31215182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149620015-T-G

http://identifiers.org/hco/13/GRCh38#31215751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149621611-C-A

31215826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149621689-G-A

31216133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149622442-T-G

31216134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149622443-T-A

http://identifiers.org/hco/13/GRCh38#31216320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149622634-C-A

31219433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149622770-A-G

31220354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623181-C-G

31220431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623247-T-A

31220737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623567-T-A

31220767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623596-T-C

31220825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623650-A-G

31220899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623721-A-T

31221176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623929-T-G

31221206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149623959-G-A

31221328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149624076-G-A

31221533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149624252-G-A

http://identifiers.org/hco/13/GRCh38#31221665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149624378-C-A

31221665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149624378-C-T

31221842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149624558-A-G

31221920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149624590-A-G

31222754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626552-A-G

http://identifiers.org/hco/13/GRCh38#31222831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149626630-C-A

31222831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626630-C-G

31222831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626630-C-T

31222845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626643-T-A

31222893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626684-G-A

31222900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626691-T-C

31222968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: missense variant
orthologous variants: 149626760-G-A

31222975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 149626767-A-G

31223007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149626800-T-C

31225186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149627639-G-A

31225283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149627734-A-G

31225309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149627760-G-A

31225312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149627767-T-G

31225438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149627904-G-T

31225472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149627936-C-G

31225647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628047-C-G

31225744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628068-G-A

31225819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628127-G-A

31225820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628128-G-A

31225869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628176-C-G

31225924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628230-G-A

http://identifiers.org/hco/13/GRCh38#31225972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149628275-C-A

31225972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628275-C-T

31226138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628413-C-T

31226147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628422-G-A

31226147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628422-G-C

31226147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628422-G-T

31226219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628497-A-G

31226237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628515-G-A

31226274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628541-C-T

http://identifiers.org/hco/13/GRCh38#31226438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149628685-C-A

31226505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149628754-T-A

31226969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149629021-C-T

31227827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149630742-T-G

31227881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149630796-T-G

31227894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149630804-G-C

31227947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149630820-T-A

31228007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149630879-G-T

31228370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149631171-G-C

31228376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149631177-G-A

31228746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632166-G-A

31228880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632272-T-G

31228965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632319-C-T

31228998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632351-G-A

31229027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632381-G-T

31229073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632670-A-T

http://identifiers.org/hco/13/GRCh38#31229086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149632683-C-A

31229086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632683-C-G

31229086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632683-C-T

http://identifiers.org/hco/13/GRCh38#31229114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149632713-C-A

31229114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632713-C-T

http://identifiers.org/hco/13/GRCh38#31229115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149632714-A-C

31229115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632714-A-G

31229115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632714-A-T

31229128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632727-T-G

http://identifiers.org/hco/13/GRCh38#31229303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149632903-C-A

31229303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632903-C-G

31229303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632903-C-T

http://identifiers.org/hco/13/GRCh38#31229321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149632925-C-A

31229321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632925-C-G

31229321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632925-C-T

31229350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149632953-G-T

31232835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149635498-C-T

31232950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149635628-C-T

31236020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149636460-T-G

31236036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149636475-A-G

31236536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149636937-C-T

31236556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149636960-C-G

31236556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149636960-C-T

31236748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149637156-T-A

31238203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149637882-C-G

31238296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149637977-A-G

31238385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638046-C-G

31238414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638072-A-G

31238558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638227-G-A

31238607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638285-T-C

31238710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638339-G-A

31238907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638390-G-C

31239383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638908-G-A

31239405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149638928-A-G

31239662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639130-A-G

31239675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639147-C-T

31239679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639151-T-G

31239807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639226-A-G

31239813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639232-A-G

31240046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639467-G-T

31240521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149639905-A-T

31240835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149640389-T-C

31240835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149640389-T-G

http://identifiers.org/hco/13/GRCh38#31241046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149641024-A-C

31242673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149642551-C-T

31243030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149642890-C-T

31243269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149643253-C-T

31243850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149644102-T-A

31244037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149644287-G-A

31244116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149644347-T-A

31244166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149644395-T-C

31244166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149644395-T-G

31244414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149645195-C-T

http://identifiers.org/hco/13/GRCh38#31244529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149645343-A-C

31244529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149645343-A-G

31244747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149645518-A-G

31244834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149645734-T-C

31244872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149645772-C-T

http://identifiers.org/hco/13/GRCh38#31245591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149647286-A-C

31245599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149647294-C-T

31245669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149647362-C-G

31245673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149647366-C-T

31246434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149648383-T-A

31246457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149648403-C-T

31246722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149648647-G-A

http://identifiers.org/hco/13/GRCh38#31247078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149648931-C-A

31247097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 149648950-G-A

31247097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 149648950-G-T

http://identifiers.org/hco/13/GRCh38#31247149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149649005-C-A

31247149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149649005-C-G

31247149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149649005-C-T

31247150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149649006-T-A

31247150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149649006-T-C

31247173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149649039-T-A

31247567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149649898-C-G

31247724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650051-G-T

31247762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650105-G-A

31247766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650109-C-T

31247775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650118-A-G

31247777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650120-T-G

http://identifiers.org/hco/13/GRCh38#31247802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149650143-A-C

31247802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650143-A-G

31247830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650194-A-T

31247870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: synonymous variant
orthologous variants: 149650234-T-C

31247870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: stop gained
orthologous variants: 149650234-T-G

31247885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: synonymous variant
orthologous variants: 149650249-T-A

31247885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: synonymous variant
orthologous variants: 149650249-T-C

31247885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: synonymous variant
orthologous variants: 149650249-T-G

http://identifiers.org/hco/13/GRCh38#31247916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149650280-A-C

31248133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650457-G-T

http://identifiers.org/hco/13/GRCh38#31248169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149650482-C-A

31248190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650502-T-A

31248325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650660-A-G

31249152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650770-A-G

31249174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650791-G-C

31249216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650830-A-G

31249328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149650937-A-G

31249428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651018-T-C

31249514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651094-T-C

http://identifiers.org/hco/13/GRCh38#31249533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149651115-A-C

31249545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651127-G-A

31249954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651522-T-G

31249966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651534-T-C

31249967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651535-C-T

31250080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651658-A-G

31256920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149651757-A-T

http://identifiers.org/hco/13/GRCh38#31257165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149652010-C-A

31257165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652010-C-T

31260175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652392-C-G

31260196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652419-G-A

31260197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652420-G-A

31260197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652420-G-T

31260257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652481-A-G

http://identifiers.org/hco/13/GRCh38#31260381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149652517-C-A

31260381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652517-C-T

http://identifiers.org/hco/13/GRCh38#31260395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149652531-C-A

31260395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149652531-C-T

31260415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149652551-G-T

31260426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149652562-T-C

31260426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 149652562-T-G

http://identifiers.org/hco/13/GRCh38#31260512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149652616-A-C

31260698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653142-T-G

31260793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653241-T-A

31260811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653259-A-G

31260924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653367-A-G

31260933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653376-C-G

http://identifiers.org/hco/13/GRCh38#31261011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149653454-C-A

31261011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149653454-C-T

31261065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149653508-T-C

31261071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149653514-A-G

31261099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653542-A-T

31261105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653548-T-C

31261105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653548-T-G

http://identifiers.org/hco/13/GRCh38#31261156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149653581-C-A

31261156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653581-C-T

31261225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653636-G-T

31261238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149653649-G-A

http://identifiers.org/hco/13/GRCh38#31268645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

31269094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656008-A-G

31269094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656008-A-T

31269149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656057-G-T

31269197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656121-T-C

31269307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656295-T-C

31269307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656295-T-G

31269344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656344-T-C

31269371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656371-T-G

http://identifiers.org/hco/13/GRCh38#31269392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149656395-C-A

31269392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656395-C-T

31269504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656467-A-G

31269539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656498-G-A

31269557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656516-T-C

31269557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149656516-T-G

31274425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149658748-G-A

31274425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149658748-G-T

31274495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149658821-C-T

31274574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149658900-C-T

http://identifiers.org/hco/13/GRCh38#31274619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149658945-A-C

31274619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149658945-A-G

31274619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149658945-A-T

31274662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149658986-A-G

31274681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149659026-T-C

http://identifiers.org/hco/13/GRCh38#31274697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149659044-C-A

31274697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149659044-C-G

31274697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149659044-C-T

31275756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149660416-G-T

31276132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149661853-T-C

31276140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149661861-A-G

31276261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149661963-G-A

31276505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662785-G-C

31276516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662796-G-T

31276528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662809-G-A

http://identifiers.org/hco/13/GRCh38#31276554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149662836-C-A

31276554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662836-C-T

31276592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662867-G-A

31276592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662867-G-T

http://identifiers.org/hco/13/GRCh38#31276627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149662896-C-A

31276627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662896-C-T

31276654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662928-T-A

31276654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662928-T-G

http://identifiers.org/hco/13/GRCh38#31276660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149662934-C-A

31276660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149662934-C-T

31276838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663132-A-G

http://identifiers.org/hco/13/GRCh38#31276872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663158-A-C

31276872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663158-A-T

http://identifiers.org/hco/13/GRCh38#31276881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663169-C-A

31276881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663169-C-T

31276883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663171-G-A

31276883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663171-G-T

31276901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663188-G-A

31276901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663188-G-T

http://identifiers.org/hco/13/GRCh38#31276909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663196-A-C

http://identifiers.org/hco/13/GRCh38#31276921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663208-C-A

31276921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663208-C-G

31276921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663208-C-T

http://identifiers.org/hco/13/GRCh38#31276922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663209-A-C

31276922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663209-A-G

31276922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663209-A-T

31276977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663264-G-A

31276977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663264-G-C

31276977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663264-G-T

31276981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663268-G-C

31277036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663328-C-T

http://identifiers.org/hco/13/GRCh38#31277131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663404-C-A

31277233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663497-G-A

31277289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663538-G-T

31277454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663687-A-T

31277565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663824-G-A

http://identifiers.org/hco/13/GRCh38#31277586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149663844-C-A

31277586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663844-C-G

31277659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149663930-A-G

31278566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149664903-T-G

31279171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149666434-A-G

31280370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149666538-C-T

31280549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149666679-A-T

31280555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149666685-T-C

http://identifiers.org/hco/13/GRCh38#31280843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149666946-A-C

31280996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149667002-C-T

31281035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149667041-G-A

31281300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149667305-C-T

http://identifiers.org/hco/13/GRCh38#31281311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149667319-C-A

31281593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149667558-G-A

31284588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149668832-G-T

http://identifiers.org/hco/13/GRCh38#31284628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149668871-C-A

31284628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149668871-C-T

http://identifiers.org/hco/13/GRCh38#31284630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149668873-C-A

31284630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 149668873-C-G

31284682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149668925-A-G

31284730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 149668973-T-C

31284760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 149669003-A-G

31284777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669020-T-C

31284778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669021-A-G

31284783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669024-T-G

31284834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669066-A-G

http://identifiers.org/hco/13/GRCh38#31286623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149669872-A-C

31286623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669872-A-G

31286623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669872-A-T

31286708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669958-T-C

http://identifiers.org/hco/13/GRCh38#31286710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149669960-C-A

31286710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669960-C-T

http://identifiers.org/hco/13/GRCh38#31286711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149669961-C-A

31286711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149669961-C-T

31286894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149670121-T-A

31286894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149670121-T-C

31286920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149670144-A-G

31313012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149672787-A-G

31313012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149672787-A-T

http://identifiers.org/hco/13/GRCh38#31313019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149672794-C-A

31317387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149673789-T-A

31317422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149673816-T-C

31317422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149673816-T-G

http://identifiers.org/hco/13/GRCh38#31317443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149673832-C-A

31317443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149673832-C-T

31317451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149673839-A-T

31317662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 149673992-C-T

31317752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149674505-G-A

31317765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149674518-G-A

31317857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149674615-C-T

31317970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149674736-T-G

31323729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149677510-T-C

31323800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: stop gained
orthologous variants: 149677579-C-T

31323826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: synonymous variant
orthologous variants: 149677605-T-C

31323826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: missense variant
orthologous variants: 149677605-T-G

31323915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149677690-T-C

31325086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678194-T-C

31325265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678366-T-C

31325353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678456-C-G

31325404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678501-G-C

31325725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678775-G-A

31325725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678775-G-T

31325845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678888-A-T

31325854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149678897-A-G

31328745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149680356-G-T

31328760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149680371-A-G

31328847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149680472-A-G

31329362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149681182-G-T

31329387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149681207-A-G

31329388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149681208-T-C

31329389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron variant
orthologous variants: 149681209-A-T

31329496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 149682899-T-C

31329496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 149682899-T-G

31329628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: missense variant
orthologous variants: 149683031-C-T

http://identifiers.org/hco/13/GRCh38#31329725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149683109-C-A

31329725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683109-C-T

http://identifiers.org/hco/13/GRCh38#31329861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149683218-C-A

31329861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683218-C-T

31329873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683230-A-G

31329975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683336-G-A

31329975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683336-G-T

31329996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683356-G-A

31329996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683356-G-C

31330034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683516-A-G

http://identifiers.org/hco/13/GRCh38#31330093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149683585-A-C

31330169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683721-G-A

31330190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683739-G-A

31330190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683739-G-T

31330263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683800-G-A

http://identifiers.org/hco/13/GRCh38#31330299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149683831-C-A

31330299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149683831-C-T

http://identifiers.org/hco/13/GRCh38#31330321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149683852-C-A

http://identifiers.org/hco/13/GRCh38#31330333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149683864-C-A

31330732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684244-A-G

31330802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684340-G-A

31330933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684458-T-C

31331064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684610-G-A

31331064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684610-G-T

31331123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684671-G-T

31331160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684699-T-C

31331160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684699-T-G

31331196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684742-A-G

31331278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149684829-G-T

31331437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685008-C-T

31331512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685102-T-G

31331527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685116-T-C

31331705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685296-A-G

31331722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685308-A-G

http://identifiers.org/hco/13/GRCh38#31331864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149685461-C-A

http://identifiers.org/hco/13/GRCh38#31331882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#149685479-C-A

31331882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685479-C-T

31332090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685676-G-T

31332106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685692-A-T

31332117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20207
most severe consequence: 3 prime UTR variant
orthologous variants: 149685704-A-G