114821831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 57349530-G-A

114821831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 57349530-G-T

114821950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 57349626-G-A

114821950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 57349626-G-C

114821950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 57349626-G-T

114822024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 57349703-G-A

114822024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 57349703-G-T

http://identifiers.org/hco/10/GRCh38#114822093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57349772-C-A

114822093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 57349772-C-G

114822093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57349772-C-T

114822129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349808-G-A

114822129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349808-G-C

114822129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349808-G-T

114822138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349819-T-C

114822138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349819-T-G

114822141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349822-G-A

114822141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349822-G-C

114822141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349822-G-T

http://identifiers.org/hco/10/GRCh38#114822152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57349833-A-C

114822152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57349833-A-G

114822152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57349833-A-T

114822159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349841-G-A

114822159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57349841-G-T

114822618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57350018-G-A

http://identifiers.org/hco/10/GRCh38#114822870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57350218-A-C

114822930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57350277-T-C

114823240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57350597-C-T

114823241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57350598-A-G

114823313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57350650-T-G

http://identifiers.org/hco/10/GRCh38#114823376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57350706-A-C

114824611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57351532-C-T

114824892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57351793-A-G

114825441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57352779-C-T

114825628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57352968-G-C

114825628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57352968-G-T

114825842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353139-T-C

114825863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57353160-C-G

114825863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57353160-C-T

114826020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353289-A-G

http://identifiers.org/hco/10/GRCh38#114826530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57353753-C-A

114826565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353785-G-T

114826589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353800-T-C

114826677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353882-G-A

114826722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353929-A-T

114826811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57353989-T-G

http://identifiers.org/hco/10/GRCh38#114826866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57354117-C-A

114826866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57354117-C-T

114826943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57354212-G-A

114828172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57355264-A-G

114828345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57355403-C-T

114828392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57355449-A-G

114828432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57355470-A-G

http://identifiers.org/hco/10/GRCh38#114828900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57355717-A-C

114829816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356270-T-C

114829934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356390-T-A

114829968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356417-G-T

114830093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356541-T-C

114830107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356555-T-C

114830457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356666-G-A

114830652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356763-T-G

114830695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356802-A-G

114830780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356883-A-G

114830780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356883-A-T

114830781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356884-A-G

http://identifiers.org/hco/10/GRCh38#114830816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57356922-C-A

114830816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57356922-C-T

http://identifiers.org/hco/10/GRCh38#114830822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57356928-C-A

http://identifiers.org/hco/10/GRCh38#114830908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57357012-C-A

114830908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57357012-C-T

114830938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57357039-A-G

http://identifiers.org/hco/10/GRCh38#114830953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57357050-A-C

114831256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57357306-G-A

114833154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57359505-G-A

114833154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57359505-G-T

114833163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57359510-A-G

114833228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57359581-T-A

114833294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57359647-A-G

114833384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57359737-T-C

http://identifiers.org/hco/10/GRCh38#114833506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57359830-C-A

114833537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57359861-A-G

114833576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57359904-A-G

114833582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57359910-A-G

114833712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360027-G-A

114833713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360028-G-T

114833728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360046-A-G

114833738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360057-A-G

114834154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360401-G-A

114834208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360450-C-T

114834326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360572-T-G

114834525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360777-C-T

114834617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360858-G-A

114835056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57360967-A-G

114835278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361123-C-T

http://identifiers.org/hco/10/GRCh38#114835394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57361256-C-A

114835394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361256-C-T

114835450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361312-T-C

114835450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361312-T-G

114835591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57361426-A-G

http://identifiers.org/hco/10/GRCh38#114835655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57361492-C-A

114835655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361492-C-T

114835671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361511-T-C

114835697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361529-T-A

114835721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361553-G-A

114835721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361553-G-C

http://identifiers.org/hco/10/GRCh38#114835741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57361577-C-A

114835741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361577-C-T

114835853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361657-C-T

114836204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57361792-G-A

http://identifiers.org/hco/10/GRCh38#114836226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57361814-C-A

114836226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57361814-C-T

114836324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57361881-T-C

114836617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57362096-T-C

114836890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57362326-A-G

114838408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57362990-G-A

114838604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57364057-G-C

114840784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365134-G-A

114841012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365358-C-G

114841596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365764-G-A

114841663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365808-T-A

114841684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365829-A-G

114841798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365902-T-C

114841809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365913-T-G

114841824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365929-G-T

114841859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365960-T-G

114841876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365980-T-C

114841883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57365986-A-G

114842941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57366989-G-A

114842941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57366989-G-C

114843012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: stop gained
orthologous variants: 57367060-C-G

114843019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57367067-T-C

114843109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57367157-T-A

114843127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57367175-G-C

114843738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57367408-T-A

114843738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 57367408-T-C

114843881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57367551-C-G

http://identifiers.org/hco/10/GRCh38#114843917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57367587-C-A

114843917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57367587-C-G

114843917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57367587-C-T

http://identifiers.org/hco/10/GRCh38#114843943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57367613-C-A

http://identifiers.org/hco/10/GRCh38#114843964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57367637-A-C

114843964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57367637-A-G

114843964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57367637-A-T

114843970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57367643-G-A

114845114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57368824-T-C

114845114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57368824-T-G

114845322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57368995-G-A

114845397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57369062-T-C

114845412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57369077-A-G

http://identifiers.org/hco/10/GRCh38#114845563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57369212-C-A

114845563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369212-C-T

114846148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369631-C-G

114846148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369631-C-T

114846217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57369706-C-T

114846280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57369769-A-G

114846377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369866-G-A

http://identifiers.org/hco/10/GRCh38#114846404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57369890-C-A

114846415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369901-G-A

114846415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369901-G-T

114846420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57369910-T-G

114846589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57370186-C-G

114846589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57370186-C-T

114846634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57370231-T-C

114846663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57370260-A-G

114846663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57370260-A-T

114846756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370346-C-G

114846772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370359-G-T

http://identifiers.org/hco/10/GRCh38#114846790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57370377-C-A

114846790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370377-C-T

114846795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370382-A-G

114846804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370391-C-T

http://identifiers.org/hco/10/GRCh38#114846876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57370446-C-A

114847050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370612-A-G

http://identifiers.org/hco/10/GRCh38#114847073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57370634-C-A

114847073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57370634-C-G

http://identifiers.org/hco/10/GRCh38#114847136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57370697-A-C

114847159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57370720-T-C

114847180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57370738-T-C

114848371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57371405-G-A

114848449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57371472-C-G

114848671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57371623-C-G

114848671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57371623-C-T

114848710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57371662-C-T

http://identifiers.org/hco/10/GRCh38#114848725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57371677-C-A

114848725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57371677-C-T

114848778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57371735-T-C

http://identifiers.org/hco/10/GRCh38#114848790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57371750-C-A

114848790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57371750-C-T

http://identifiers.org/hco/10/GRCh38#114848793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57371753-C-A

114848793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57371753-C-G

http://identifiers.org/hco/10/GRCh38#114848817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57371774-C-A

114848817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57371774-C-T

114854559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372079-T-C

114854559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372079-T-G

114854901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372371-A-G

114855071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372456-G-A

114855071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372456-G-T

114855088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372473-G-A

114855088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372473-G-T

114855177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372535-A-G

114855215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57372570-A-G

114855215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57372570-A-T

114855238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57372593-T-A

114855238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57372593-T-C

114855251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57372606-G-A

114855295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57372650-T-A

114855295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57372650-T-G

114855361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372716-A-T

114855462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372782-G-C

114855462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372782-G-T

114855476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372794-G-A

114855476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372794-G-T

http://identifiers.org/hco/10/GRCh38#114855477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57372795-C-A

114855477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372795-C-T

114855483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372801-T-A

114855483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57372801-T-C

114859231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373079-T-C

114859251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373094-T-G

114860842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: missense variant
orthologous variants: 57373779-G-A

114860932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373866-T-C

114860955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373889-A-G

114860957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373891-T-C

114860957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373891-T-G

114860966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57373900-T-G

114861209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57374686-G-A

114861211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57374688-G-A

114861245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57374726-T-C

http://identifiers.org/hco/10/GRCh38#114861257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57374738-C-A

114861305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57374786-G-A

114861305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: synonymous variant
orthologous variants: 57374786-G-T

114861375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57374856-G-A

114861386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57374864-G-T

114861450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57374918-A-G

114861450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57374918-A-T

114861504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57374972-C-T

114861528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 57374996-C-T

114861662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375088-G-A

114861730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375150-G-A

http://identifiers.org/hco/10/GRCh38#114861836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57375248-A-C

114861836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375248-A-G

114862086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375498-T-G

114862090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375502-G-C

114862192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375601-C-G

http://identifiers.org/hco/10/GRCh38#114862278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57375687-C-A

114862467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375878-C-T

http://identifiers.org/hco/10/GRCh38#114862481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57375892-C-A

114862481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375892-C-T

114862538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57375949-T-C

http://identifiers.org/hco/10/GRCh38#114862643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57376086-C-A

114862643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376086-C-G

http://identifiers.org/hco/10/GRCh38#114862693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57376127-C-A

114862753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376193-T-G

114862766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376206-C-G

114862775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376217-G-A

114862789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376230-T-C

http://identifiers.org/hco/10/GRCh38#114862796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57376237-C-A

114862830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376262-G-A

114862830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376262-G-T

114862922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376322-A-G

114862947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376344-G-C

114862953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376350-T-G

114863151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376555-A-G

http://identifiers.org/hco/10/GRCh38#114863199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57376599-C-A

114863199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376599-C-T

114863206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376606-T-C

114863222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376622-G-C

114863249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376649-G-C

114863249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376649-G-T

114863253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376652-T-A

http://identifiers.org/hco/10/GRCh38#114863297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57376697-C-A

114863297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376697-C-G

114863297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376697-C-T

http://identifiers.org/hco/10/GRCh38#114863371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57376770-A-C

114863375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376774-T-C

114863391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376790-A-G

114863448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376839-A-G

114863468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376856-G-T

114863530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376906-T-C

114863540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57376916-A-G

114863648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57377004-G-A

114863648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57377004-G-C

114863648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 57377004-G-T

114863660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 57377016-A-T

114863706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377064-T-C

114863739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377096-T-G

114863837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377165-G-T

http://identifiers.org/hco/10/GRCh38#114864218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57377557-C-A

114864218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377557-C-G

114864218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377557-C-T

114864528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377841-G-T

114864576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377888-C-T

114864601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57377910-T-C

114864762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57378074-A-G

114865693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57382542-G-A

114865693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57382542-G-C

114865708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57382557-G-A

http://identifiers.org/hco/10/GRCh38#114865841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57382672-C-A

114865841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57382672-C-T

114867687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57385025-G-A

114868820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57385575-C-T

114868882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57385637-C-T

114868903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57385659-A-G

114869419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57386086-G-A

114869553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57386198-A-G

114869614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57386238-G-T

114869696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57386322-G-C

114869780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57386403-A-G

114869820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57386443-A-G

114869952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57386560-T-C

http://identifiers.org/hco/10/GRCh38#114869953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57386561-A-C

114870097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57386710-A-G

114874954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57390920-G-T

114875136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391097-G-A

114875326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391375-T-C

114876068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391491-G-A

114876137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391596-T-A

114876140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391599-C-G

114876183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391651-T-G

114876358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391809-C-G

114876358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57391809-C-T

http://identifiers.org/hco/10/GRCh38#114876592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57391975-C-A

114876804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57392165-C-T

114876808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57392169-A-G

114876823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57392184-C-T

114876959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57392298-G-A

114876960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57392299-G-A

114877372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron_variant, undefined
orthologous variants: 57392931-G-A

114877600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57393269-A-G

114878111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57393760-A-G

114880753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57398969-G-A

114880808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399021-A-G

114880840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399050-G-C

114880934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399125-C-T

114880942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399133-G-A

114880943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399134-G-A

http://identifiers.org/hco/10/GRCh38#114880978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57399170-A-C

114880978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399170-A-T

http://identifiers.org/hco/10/GRCh38#114881111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57399303-C-A

114881111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399303-C-T

http://identifiers.org/hco/10/GRCh38#114881245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57399442-C-A

114881245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399442-C-T

114881351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57399545-T-C

http://identifiers.org/hco/10/GRCh38#114881556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57399870-C-A

114881698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57400013-G-T

114881804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57400127-C-T

114881878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57400220-C-T

114882067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57400365-C-T

114892225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57403112-A-G

114893200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57403756-A-G

http://identifiers.org/hco/10/GRCh38#114893213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57403769-C-A

114893377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57403934-G-A

114893377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57403934-G-T

114893378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57403935-T-G

114893426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57404125-C-T

114893757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57404419-G-A

114894064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57405769-A-T

114894252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57405943-C-T

114895117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57407398-C-G

114895301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57407612-G-A

http://identifiers.org/hco/10/GRCh38#114895416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#57407699-A-C

114895416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57407699-A-G

114895556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57407831-G-A

114895590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29320
most severe consequence: intron variant
orthologous variants: 57407863-C-G