http://identifiers.org/hco/12/GRCh38#107318485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85222744-C-A

107318485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222744-C-T

http://identifiers.org/hco/12/GRCh38#107318490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85222749-C-A

107318490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222749-C-T

http://identifiers.org/hco/12/GRCh38#107318497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85222756-C-A

107318497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222756-C-T

http://identifiers.org/hco/12/GRCh38#107318520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85222774-A-C

107318520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 85222774-A-T

107318569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222820-C-T

107318589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222840-G-A

107318589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222840-G-T

107318615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222866-G-A

107318627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222878-G-T

107318630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222881-G-A

107318630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222881-G-T

107318654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222904-G-A

107318654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222904-G-T

http://identifiers.org/hco/12/GRCh38#107318669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85222919-C-A

107318669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222919-C-G

107318669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222919-C-T

107318673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85222923-G-A

107318757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85223008-G-A

107318757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5 prime UTR variant
orthologous variants: 85223008-G-T

107318964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223216-C-G

107318986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense variant
orthologous variants: 85223238-C-G

107318991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223243-G-A

107319063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223315-G-A

107319063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223315-G-C

107319063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223315-G-T

http://identifiers.org/hco/12/GRCh38#107319444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85223696-C-A

107319444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223696-C-T

107319447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223699-G-A

107319447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223699-G-C

107319447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223699-G-T

107319568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense_variant, undefined
orthologous variants: 85223820-A-G

107319618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223870-G-A

107319618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85223870-G-T

107319810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85224065-G-A

107319810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85224065-G-T

http://identifiers.org/hco/12/GRCh38#107319864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224119-C-A

107319864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense variant
orthologous variants: 85224119-C-G

107319864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85224119-C-T

http://identifiers.org/hco/12/GRCh38#107319921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224188-A-C

107319921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85224188-A-G

http://identifiers.org/hco/12/GRCh38#107319926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224193-C-A

107319926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense variant
orthologous variants: 85224193-C-G

107319926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: missense variant
orthologous variants: 85224193-C-T

http://identifiers.org/hco/12/GRCh38#107320144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224382-C-A

107320144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224382-C-T

107320271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224504-C-T

107320462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224717-G-C

107320462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224717-G-T

http://identifiers.org/hco/12/GRCh38#107320530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224780-A-C

107320530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224780-A-T

http://identifiers.org/hco/12/GRCh38#107320545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224796-C-A

107320578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224829-C-T

107320589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224840-T-C

107320589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85224840-T-G

107320602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, missense_variant
orthologous variants: 85224853-G-T

107320610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85224859-C-T

http://identifiers.org/hco/12/GRCh38#107320624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85224873-A-C

107320896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85225109-C-G

107321081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85225280-A-G

107321081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85225280-A-T

107322266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85226550-C-T

107323016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85227606-T-C

107323704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85229455-C-T

107323826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85229548-T-G

107323926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85229643-A-G

107324044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85229731-C-T

107324177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85229848-T-C

107324264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85229959-C-T

http://identifiers.org/hco/12/GRCh38#107324548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85230106-A-C

107324562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85230120-G-A

107324828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85230358-T-C

107324899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85230428-G-T

107325007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85230541-G-A

107325411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85230948-A-G

107325591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231126-G-A

107325778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231322-T-C

107326239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231473-C-T

107326279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231499-A-G

107326640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231800-G-A

107326680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231848-G-C

107326710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231875-G-A

107326817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85231974-C-T

http://identifiers.org/hco/12/GRCh38#107326855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85232011-C-A

http://identifiers.org/hco/12/GRCh38#107326955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85232104-C-A

http://identifiers.org/hco/12/GRCh38#107326961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85232110-C-A

107326981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85232131-G-A

107327153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85232300-G-T

107327270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85232815-C-T

107327453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85232992-C-G

107327504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233030-T-C

107327506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233032-C-T

http://identifiers.org/hco/12/GRCh38#107327526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85233051-A-C

107327580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233105-T-G

107327660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233171-G-A

107327671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233182-G-A

107327671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233182-G-T

107327746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233232-C-T

107327809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85233294-C-T

107328039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85233537-G-A

107330350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85234675-T-A

107330350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85234675-T-C

107330630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85234900-G-C

107331029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85235314-G-A

107331029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85235314-G-T

107331110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85235392-A-T

107331117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85235399-G-A

107335359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85236336-A-G

107335419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85236395-G-C

107335420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85236396-C-T

107335855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85236713-G-A

107335998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85236808-C-T

107336302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85237156-T-C

107336348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85237204-T-G

107336387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85237221-C-T

107337114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85237797-T-C

http://identifiers.org/hco/12/GRCh38#107337125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85237808-A-C

http://identifiers.org/hco/12/GRCh38#107337177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85237845-C-A

107337177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85237845-C-T

107337251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85237923-T-C

107337338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85238007-C-T

107337508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85238166-A-G

107337542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85238200-C-T

107337630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85238287-G-A

107338010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85238940-T-G

http://identifiers.org/hco/12/GRCh38#107338188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85239137-C-A

107338228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239175-C-T

107338328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239275-C-T

107338329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239276-G-A

107338329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239276-G-T

107338464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239399-T-C

107338581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239531-G-C

107338596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239546-G-A

107338606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239555-T-C

107338667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239597-C-T

107339101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239815-C-T

107339168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239884-C-T

107339241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239956-T-C

107339268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85239983-G-T

107339500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85240159-T-G

107339512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85240171-C-G

107339626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85240293-T-C

107339683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85240364-G-A

107339715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85240391-T-A

107339779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85241180-G-A

http://identifiers.org/hco/12/GRCh38#107339895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85241268-A-C

107339897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85241270-C-T

107339970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85241337-G-A

107340492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85241818-C-T

107340617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85241925-A-T

107340713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85241995-T-A

107342329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242708-G-A

107342345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242721-G-C

107342345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242721-G-T

107342359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242735-G-A

107342371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242747-C-T

http://identifiers.org/hco/12/GRCh38#107342437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85242804-C-A

107342448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242815-C-T

107342600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242938-C-T

107342618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85242956-A-G

107343174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85243427-C-T

107343369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85243565-G-T

107345645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244057-T-C

107345701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244113-A-G

107345877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244284-A-G

107345883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244320-G-A

107345891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244328-C-T

107345991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244416-C-T

http://identifiers.org/hco/12/GRCh38#107346072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85244489-C-A

107346850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244888-G-T

http://identifiers.org/hco/12/GRCh38#107346865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85244898-C-A

107346865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244898-C-G

107346891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85244912-C-T

http://identifiers.org/hco/12/GRCh38#107347112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85245133-A-C

107347148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245158-A-G

107347268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245288-T-A

107347594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245898-T-C

107347598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245902-G-A

107347629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245932-G-T

107347630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245933-G-C

107347685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245972-C-T

107347696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85245985-G-T

107347778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246017-G-A

http://identifiers.org/hco/12/GRCh38#107347857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85246089-A-C

107347857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246089-A-G

107347905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246221-C-T

107348030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246554-G-A

107348126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246680-G-A

107348145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246701-A-G

107348215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246768-G-A

107348227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246780-A-G

107348259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85246805-A-T

107349047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85248557-C-T

107349102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85248626-T-C

107349162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85248684-G-T

107349213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85248742-C-T

107349381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85248887-G-A

107349381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85248887-G-C

http://identifiers.org/hco/12/GRCh38#107350001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85255755-C-A

107350001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85255755-C-T

107350225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85255951-T-C

107350259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85255985-T-C

107350259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85255985-T-G

http://identifiers.org/hco/12/GRCh38#107352521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85256566-C-A

107352586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85256613-A-G

107352837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85256809-G-A

http://identifiers.org/hco/12/GRCh38#107352873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85256854-C-A

107352873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85256854-C-T

107355239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85257224-A-G

107355240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85257225-T-C

107355243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85257228-G-C

107355645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85257592-T-C

107356108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85257900-A-G

107356470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85258637-G-A

107356477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85258644-A-G

107356480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85258650-G-A

107356810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85258924-G-A

107356979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259072-T-C

http://identifiers.org/hco/12/GRCh38#107357792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85259106-A-C

107357792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259106-A-G

107357792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259106-A-T

107357912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259212-C-T

107357956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259243-C-T

http://identifiers.org/hco/12/GRCh38#107357972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85259265-C-A

107357995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259288-C-T

107358544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85259739-A-T

107359039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260120-G-A

107359232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260303-A-G

107359365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260436-C-G

107359476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260814-G-A

107359595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260929-C-G

107359595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260929-C-T

107359604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260938-T-C

107359648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85260986-C-T

107359874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85261364-G-A

107359975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85261461-C-T

107360183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85262375-G-T

107360216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85262405-G-C

http://identifiers.org/hco/12/GRCh38#107360285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85262470-A-C

107360497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85262717-C-T

107361305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263137-A-G

107361318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263150-T-C

107361390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263218-A-G

107361629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263605-T-C

107361932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263947-C-T

107361960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263972-A-G

http://identifiers.org/hco/12/GRCh38#107361969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85263980-C-A

107361970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85263981-A-G

107362159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264145-G-A

107362387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264343-A-G

http://identifiers.org/hco/12/GRCh38#107362829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85264735-C-A

107362829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264735-C-T

107362831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264737-C-T

107362945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264848-C-G

107362996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264899-C-G

107362996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85264899-C-T

107363703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85265787-C-T

107363734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85265817-T-C

107364231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85266340-A-G

107364825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85266576-T-C

107364829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85266580-G-C

107365023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85266765-T-C

107365119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270008-G-A

107365254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270144-G-A

107365257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270147-C-T

107365281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270171-G-C

107365422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270308-A-G

http://identifiers.org/hco/12/GRCh38#107365425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85270311-A-C

107365575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270553-C-G

107365855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270785-A-G

107365865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270795-A-G

107366087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85270968-T-G

107366147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85271015-G-A

107366147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85271015-G-T

107366167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85271035-C-T

107366488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85271329-C-T

107366666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85271507-A-T

107366703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85271544-G-T

107367808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274086-C-T

107368003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274307-C-T

107368162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274463-A-G

107368322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274624-G-A

107368416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274719-T-A

107368487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274791-C-T

http://identifiers.org/hco/12/GRCh38#107368510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85274796-C-A

107368510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85274796-C-T

107368951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85275129-C-T

107369194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85275334-T-A

http://identifiers.org/hco/12/GRCh38#107369387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85275712-C-A

107369695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85275946-A-G

107369874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276083-G-A

107370039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276215-T-C

107370112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276280-C-T

107370287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276446-T-C

107370287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276446-T-G

107370430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276587-T-C

107370595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276746-G-C

107370612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85276765-G-T

107370887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85277025-G-A

107370905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85277042-C-T

107371143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85277239-G-A

107371233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85277327-C-T

107371336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85277448-T-G

107371491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85277609-G-A

107372093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85278223-T-C

107372632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85278739-C-T

107372711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85278828-C-T

107372730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85278840-C-T

107372808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85278906-C-T

107373107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279170-A-G

107373208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279266-T-G

107373500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279368-T-C

107373547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279409-G-A

107373735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279606-G-T

107373806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279685-G-A

107373806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279685-G-C

107373806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279685-G-T

107374091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85279935-G-T

107374226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85280045-G-A

107374546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85280389-G-A

107376826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85280808-C-T

107376827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85280809-G-A

107376956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85280933-G-A

107377056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281040-G-T

107377125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281080-C-T

107377204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281155-G-T

107377219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281170-C-G

107377326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281276-C-T

107377443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281342-G-A

107377506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281393-C-T

107377798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85281714-G-A

107378193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282174-A-G

107378215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282221-A-G

107378372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282376-C-T

107378382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282386-G-A

107378536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282522-G-T

107378771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282714-G-C

107379072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85282998-G-A

http://identifiers.org/hco/12/GRCh38#107380008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85283304-C-A

107380008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85283304-C-T

107380152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85283445-G-A

107380786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85284289-G-A

http://identifiers.org/hco/12/GRCh38#107381503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85284609-A-C

107381608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85284719-G-C

107381769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85284849-T-C

107381994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285037-T-C

107382014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285058-G-A

107382034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285078-C-T

107382064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285109-A-G

107382328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285344-T-C

http://identifiers.org/hco/12/GRCh38#107382656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85285567-A-C

107383120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285812-G-C

107383209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285863-C-G

107383254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85285909-G-A

107383447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85286112-A-G

107383936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85287907-G-T

107383958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85287931-A-G

107384093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288030-G-A

107384159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288086-C-G

107384316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288222-C-T

107384736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288653-G-A

107384774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288686-G-A

107384851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288780-C-T

107384923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288854-C-T

107385043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85288963-C-T

107385275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85289136-A-G

107385317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85289178-G-A

107386886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290064-G-A

107386917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290070-G-A

107387064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290152-A-G

107387064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290152-A-T

http://identifiers.org/hco/12/GRCh38#107387144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85290169-A-C

107387280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290216-G-T

107387620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290427-G-T

107387656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290456-G-A

107387774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290565-T-G

107388427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290831-C-T

107388453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290856-T-A

107388553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290965-T-C

107388585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85290997-C-G

107388592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291008-C-T

http://identifiers.org/hco/12/GRCh38#107389008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85291270-C-A

107389008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291270-C-T

107389299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291576-A-G

107389299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291576-A-T

107389326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291601-C-T

http://identifiers.org/hco/12/GRCh38#107389361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85291639-C-A

107389361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291639-C-T

107389362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291640-A-G

107389391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291669-T-C

107389460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291734-C-T

107389472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291754-C-G

107389679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85291992-T-C

107394032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85292201-C-G

107394032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85292201-C-T

107394039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85292208-A-G

107394085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85292252-T-C

107394684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85292710-T-C

107395838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85293536-T-C

107395885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85293583-G-A

107395930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85293652-G-T

107396037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85293761-G-T

107396792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85294697-T-C

107396973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85294860-A-G

107397075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85294956-C-T

107397269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85295154-C-T

107397368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85295253-G-T

107397593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85295375-C-T

107398161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85297431-T-G

107398710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85297604-G-C

107398762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85297658-C-T

107398858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85297724-A-G

107398981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85297842-G-A

http://identifiers.org/hco/12/GRCh38#107399135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85297996-C-A

http://identifiers.org/hco/12/GRCh38#107399320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85298167-A-C

107399628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85298508-G-A

107400137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85299127-G-A

107400424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85299341-A-G

107400482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85299388-G-C

107400594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85299476-A-T

107401127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85299969-G-A

107401272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85300131-G-A

http://identifiers.org/hco/12/GRCh38#107401292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85300152-C-A

107401471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85300330-G-A

107401492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85300342-T-G

107401554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85300409-G-C

107401696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85300560-C-T

107401820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85300689-A-T

107401851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85300716-A-G

107403319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301254-G-A

107403327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301262-T-A

http://identifiers.org/hco/12/GRCh38#107403336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85301271-C-A

107403398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301335-A-G

107403398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301335-A-T

http://identifiers.org/hco/12/GRCh38#107404035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85301767-C-A

107404067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301798-G-A

107404095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301809-A-G

107404243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85301928-T-C

107404424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85302104-C-T

107404671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85302346-G-A

107406458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85302733-T-C

107406557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85302836-G-A

http://identifiers.org/hco/12/GRCh38#107406561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85302840-A-C

107406566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85302845-A-G

http://identifiers.org/hco/12/GRCh38#107406586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85302865-C-A

107407191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85303416-C-T

107407242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85303462-C-T

107407480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85303690-G-A

107407555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85303771-C-T

107407682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85303877-G-T

107407860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304011-C-T

107407991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304123-C-T

http://identifiers.org/hco/12/GRCh38#107408141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85304263-C-A

107408141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304263-C-G

107408159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304281-G-A

107408358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304483-C-T

107408712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304843-G-A

107408795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304930-C-G

107408844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85304969-T-C

107408905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85305030-A-T

107409297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85305463-C-T

http://identifiers.org/hco/12/GRCh38#107411496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85306153-C-A

http://identifiers.org/hco/12/GRCh38#107412021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85307057-A-C

107412041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85307077-G-T

107412195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307206-G-A

http://identifiers.org/hco/12/GRCh38#107412359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85307287-C-A

107412359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307287-C-T

107412394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307322-A-T

107412472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307377-C-T

107412505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307410-G-A

107412670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307490-C-G

107412716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307543-G-A

107412756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307582-T-C

107412833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307660-A-G

107413908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307886-C-T

107413909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307887-A-G

107413999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85307975-A-G

107415038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85309366-G-A

107415074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85309402-C-T

107415225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85309540-A-G

107415254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85309563-C-T

107415343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85309631-G-A

107416192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85310151-T-C

107416288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85310408-G-A

107416297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85310455-T-A

107416357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85310515-C-T

107416597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85310722-G-A

107417066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311065-C-G

107417136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311137-G-A

107417141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311142-G-A

http://identifiers.org/hco/12/GRCh38#107417160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85311161-A-C

107417160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311161-A-T

107417176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311177-A-G

107418672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311733-T-C

107418672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85311733-T-G

107419197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85312176-G-A

107419318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85312288-G-C

107419450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85312473-G-A

107419656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85312590-T-C

107419856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85312818-G-A

107420014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85312964-C-T

http://identifiers.org/hco/12/GRCh38#107420041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85312989-C-A

http://identifiers.org/hco/12/GRCh38#107420851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85313353-C-A

107420851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85313353-C-T

107420859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85313363-C-T

http://identifiers.org/hco/12/GRCh38#107420972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85313433-A-C

107420972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85313433-A-G

107421023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85313483-G-C

107421096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85313603-A-G

107421310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85313805-G-A

107421742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314211-G-A

107421940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314402-A-T

107422030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314428-T-C

107422211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314570-T-C

107422231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314590-T-C

107422266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314638-G-A

107422370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314707-G-A

107422370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314707-G-C

http://identifiers.org/hco/12/GRCh38#107422475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85314806-A-C

107422475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85314806-A-G

107422828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315090-G-A

107423071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315335-G-C

107423281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315550-A-G

107423281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315550-A-T

107423326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315598-C-T

107423344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315615-C-T

http://identifiers.org/hco/12/GRCh38#107423435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85315690-C-A

107423435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85315690-C-T

107423847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85316068-A-G

107424188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85316379-C-T

107424932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317010-T-C

107425064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317140-A-G

107425085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317162-T-C

http://identifiers.org/hco/12/GRCh38#107425109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85317174-C-A

http://identifiers.org/hco/12/GRCh38#107425169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85317234-C-A

http://identifiers.org/hco/12/GRCh38#107425240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85317310-C-A

107425387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317504-T-C

107425418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317524-G-A

107425664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317674-G-A

107425831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85317841-T-C

107426689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318572-T-C

107426690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318573-C-T

107426830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318706-C-T

107426858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318732-C-G

107427066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318928-T-C

107427071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318933-A-G

107427097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318960-C-T

107427105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85318968-G-A

107428755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319118-G-A

107428812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319175-C-T

107428859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319225-A-G

107429055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319484-G-A

107429091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319520-A-G

107429121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319553-T-G

107429127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319559-C-T

107429162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319586-G-T

107429396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85319809-A-G

107429844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85320192-A-G

107429881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85320269-T-C

107429940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85320489-G-A

107430085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85320632-T-C

107430688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85321454-T-C

107430704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85321469-A-T

107432574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85323493-A-G

107432632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85323548-A-T

107432762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85323671-A-T

107433445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85324423-C-T

107433592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85324585-T-A

107433658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85324652-T-A

107433742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85324736-T-C

107433867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85324834-A-T

107434013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85324985-C-T

107434059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325042-C-T

107434089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325072-A-G

107434923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325261-G-A

107435017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325346-G-A

107435048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325376-T-C

107435154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325470-C-T

http://identifiers.org/hco/12/GRCh38#107435224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85325536-C-A

107435224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325536-C-T

107435266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85325582-C-T

http://identifiers.org/hco/12/GRCh38#107435306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85325622-A-C

107436323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85326087-T-C

http://identifiers.org/hco/12/GRCh38#107436330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85326094-C-A

107436454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85326203-T-G

107436455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85326204-G-A

http://identifiers.org/hco/12/GRCh38#107437893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85326337-C-A

107438017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85326993-T-A

107438332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85327242-C-T

107438403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85327271-C-T

107438454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85327317-C-T

107438455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85327318-T-C

http://identifiers.org/hco/12/GRCh38#107439028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85328023-C-A

107439028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328023-C-G

107439051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328046-T-C

http://identifiers.org/hco/12/GRCh38#107439119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85328114-A-C

107439127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328122-G-C

107439500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328422-G-T

107439735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328620-T-C

107439940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328713-C-T

107440034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328794-G-A

107440076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85328836-G-A

107440300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329046-G-C

107440300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329046-G-T

107440318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329068-C-T

107440360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329104-C-G

107440360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329104-C-T

107440416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329154-C-T

107440659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329247-C-T

107440756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329340-C-T

107440833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329417-C-T

107440904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329483-C-T

107441023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329609-C-T

107441068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329642-C-G

107441068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329642-C-T

107442021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85329724-C-T

107442446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85330065-C-T

107442710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85330308-G-A

107442745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85330344-G-T

107442864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85330461-T-G

107442949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85330553-G-A

107443211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85330754-T-C

http://identifiers.org/hco/12/GRCh38#107447469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85332742-C-A

107447854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85332392-A-G

107447934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85332347-G-A

107447981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85332304-A-G

http://identifiers.org/hco/12/GRCh38#107447997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85332289-A-C

107448026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85332261-T-C

107448269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85332023-G-A

107448284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85332008-T-A

107454033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333558-G-T

107454084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333604-C-T

107454131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333652-C-T

107454179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333701-G-A

107454191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333712-G-A

http://identifiers.org/hco/12/GRCh38#107454203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85333719-C-A

107454222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333733-A-G

107454269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333767-A-G

107454275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333773-C-T

http://identifiers.org/hco/12/GRCh38#107454427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85333930-C-A

107454443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85333947-G-A

http://identifiers.org/hco/12/GRCh38#107454483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85333987-C-A

107454701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334147-G-A

107454701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334147-G-T

107454729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334179-C-T

107454781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334214-T-G

http://identifiers.org/hco/12/GRCh38#107454944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85334365-C-A

107454944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334365-C-G

http://identifiers.org/hco/12/GRCh38#107455015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85334432-A-C

107455472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334923-G-T

107455476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85334927-G-A

107455818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85335243-C-T

107457591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85336695-A-G

107457591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85336695-A-T

107457602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85336704-T-G

http://identifiers.org/hco/12/GRCh38#107457839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85336897-A-C

107458158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85337169-T-C

107458184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85337194-G-T

107461514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85337865-C-T

107461726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85338086-A-G

107461726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85338086-A-T

http://identifiers.org/hco/12/GRCh38#107461840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85338186-C-A

107461840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85338186-C-T

107461841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85338187-G-A

107461894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85338239-A-T

107462031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85338366-C-T

http://identifiers.org/hco/12/GRCh38#107462084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85338413-C-A

http://identifiers.org/hco/12/GRCh38#107467371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85340332-C-A

107467568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85340539-C-T

107467575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85340546-A-G

107467581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85340552-C-T

107467676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85340636-C-G

107467896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85340844-T-G

http://identifiers.org/hco/12/GRCh38#107468201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85341136-C-A

107468261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341198-C-T

107468396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341329-A-G

107468546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341465-G-A

107468585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341503-G-A

107468590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341511-G-A

107468590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341511-G-C

107468659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341563-T-C

107468659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341563-T-G

107468800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341747-C-G

107468902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85341978-C-T

107468972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342047-A-G

107468980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342055-G-A

107468980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342055-G-C

107468996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342071-C-T

107469003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342078-C-T

107469028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342134-A-G

107469072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342157-G-A

107469085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342169-C-G

107469471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85342468-G-A

http://identifiers.org/hco/12/GRCh38#107469477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85342474-A-C

107470391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85343998-G-C

107470523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85344080-C-G

107470639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85344201-C-T

107470883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85344446-G-A

107470889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85344452-T-G

107471008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85344563-T-G

107471054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85344609-A-G

107472975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85345669-C-T

107473040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85345729-G-C

107473063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85345758-T-A

107473172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85345848-A-G

http://identifiers.org/hco/12/GRCh38#107473306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85345979-C-A

107473307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85345980-A-G

107473361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346020-C-T

107474426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346494-C-T

107474557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346617-G-T

107474694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346722-A-G

107474771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346799-G-A

107474818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346845-C-G

107474818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85346845-C-T

107475028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347055-T-G

107475067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347091-T-C

107475113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347123-C-T

107475285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347292-C-G

107475285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347292-C-T

107475360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347358-G-A

107475360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347358-G-C

107475449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347445-C-T

107475462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347458-A-G

107475471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347467-C-G

107475474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347470-C-T

107475525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347512-A-T

107475684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85347657-A-G

107476049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85348078-G-A

http://identifiers.org/hco/12/GRCh38#107476297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85348370-A-C

107476315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85348388-C-T

107477029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85349556-G-C

107477175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85349764-C-T

107477255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350107-G-A

107477255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350107-G-T

107477280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350131-G-A

http://identifiers.org/hco/12/GRCh38#107477356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85350212-A-C

107477359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350215-G-C

107477386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350245-G-A

107477666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350499-C-G

107477817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350662-A-G

107477822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85350667-A-G

107478203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85352700-T-G

107478324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85352797-A-G

107478624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85353084-C-T

http://identifiers.org/hco/12/GRCh38#107478694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85353137-C-A

107479296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85353698-C-T

107479313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85353715-C-T

107479475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85353859-T-C

107479483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85353867-G-T

107480204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354506-G-A

107480204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354506-G-T

107480234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354532-G-A

http://identifiers.org/hco/12/GRCh38#107480290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85354587-A-C

107480528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354807-C-G

107480683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354952-C-T

107480687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354959-A-T

107480734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85354994-T-C

107480756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85355004-T-C

107480867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85355123-C-T

107481543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85355464-G-A

107481569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85355473-G-C

107481963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85355906-C-T

107482098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85356027-G-A

http://identifiers.org/hco/12/GRCh38#107482122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85356053-C-A

107482141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85356075-G-A

107482168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85356099-C-T

107485525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85357933-G-A

107485529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85357937-C-T

107485570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85357988-T-C

107485570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85357988-T-G

107485842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85358253-C-T

107485927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85358337-A-G

107485969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85358368-G-A

107485977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85358376-G-A

107487122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85358831-C-T

107487156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85358865-A-G

http://identifiers.org/hco/12/GRCh38#107487917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85359972-A-C

107488006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85360053-C-T

107488105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85360149-C-T

107488140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85360167-G-A

107488140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85360167-G-C

107492211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85361484-A-G

107492574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85361804-C-T

107492590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85361839-C-T

107492636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85361894-C-T

107492649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85361907-A-T

107492770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362010-G-A

http://identifiers.org/hco/12/GRCh38#107492781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85362021-C-A

107492791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362031-G-A

107492967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362194-G-A

107492976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362203-G-C

107492976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362203-G-T

107494445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362720-C-T

http://identifiers.org/hco/12/GRCh38#107494500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85362769-C-A

107494541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362809-G-A

107494568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362822-G-A

http://identifiers.org/hco/12/GRCh38#107494713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85362851-C-A

107494713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85362851-C-T

107494887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85363335-G-A

107495406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85363925-C-T

107495447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85363965-G-A

107495454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85363972-A-G

107495635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364107-C-T

107495675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364145-T-C

107499185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364809-T-G

107499224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364847-T-C

107499224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364847-T-G

107499230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364853-C-T

107499345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85364971-A-G

107499381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85365020-T-C

http://identifiers.org/hco/12/GRCh38#107499423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85365071-A-C

http://identifiers.org/hco/12/GRCh38#107500596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85365806-C-A

107500626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85365840-C-T

107500761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85365920-G-A

107500784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85365945-A-T

107500944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85366066-C-T

107501014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85366136-G-T

107501152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85366245-C-T

107501282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85366357-A-G

http://identifiers.org/hco/12/GRCh38#107504062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85367839-C-A

107504231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85368020-G-A

107504396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85368180-C-G

107504574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369083-G-A

107504648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369152-A-G

107504649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369153-T-C

107504887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369394-A-G

107504925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369432-C-T

107505102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369600-G-A

107505248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369722-G-A

http://identifiers.org/hco/12/GRCh38#107505280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85369752-A-C

107505296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369768-A-G

107505334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369807-C-G

107505428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369907-C-T

107505503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85369976-A-T

107507022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85371924-T-G

107507023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85371925-G-T

107507097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372012-T-A

107507097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372012-T-G

107507135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372050-G-A

http://identifiers.org/hco/12/GRCh38#107507246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85372259-C-A

107507408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372594-C-T

107507633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372775-C-T

107507675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372817-G-A

107507815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372906-C-G

107507815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372906-C-T

107507846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372922-A-G

http://identifiers.org/hco/12/GRCh38#107507871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85372947-C-A

107507898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85372974-G-T

107507973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85373048-T-C

http://identifiers.org/hco/12/GRCh38#107508017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85373092-A-C

107508237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85373271-A-T

107508276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85373310-C-T

107508286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85373320-G-A

107508354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85373395-G-A

http://identifiers.org/hco/12/GRCh38#107508974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85373754-C-A

107509207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85373958-G-C

107510098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85376629-G-A

107510139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85376660-C-G

107510139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85376660-C-T

107510369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85376855-C-T

http://identifiers.org/hco/12/GRCh38#107513760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85377828-C-A

107513877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85377944-T-A

107513877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85377944-T-C

107513879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85377946-T-C

107513994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85378057-T-A

107514089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85378157-A-G

107514401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85378444-G-A

107515003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85380013-A-G

107515049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85380048-G-A

107515049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85380048-G-T

107515295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85380257-A-G

107515350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85380310-C-T

107519704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85381403-G-A

107519837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85381538-A-G

107520125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85381810-G-C

107520143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85381827-G-A

107520143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85381827-G-C

107520246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85381918-T-C

107520246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85381918-T-G

107520255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85381927-G-A

107520314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382134-G-C

107520339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382193-T-C

107520339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382193-T-G

107520343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382197-G-T

107520352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382206-T-C

107520352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382206-T-G

107520391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382226-G-T

http://identifiers.org/hco/12/GRCh38#107520424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85382249-C-A

107520424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382249-C-T

107520442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382267-A-G

107520665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382484-A-G

http://identifiers.org/hco/12/GRCh38#107520784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85382594-C-A

107520784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382594-C-T

http://identifiers.org/hco/12/GRCh38#107520790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85382600-A-C

107520807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85382618-G-A

http://identifiers.org/hco/12/GRCh38#107520871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85382695-A-C

107523036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85384689-A-G

107523180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85384825-A-G

107523185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85384830-C-G

107523209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85384851-G-A

107523229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85384882-A-G

107523260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385297-T-G

107523313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385350-T-C

107523313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385350-T-G

107523342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385382-G-C

107523478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385512-G-A

107523586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385817-T-C

107523730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85385954-C-T

http://identifiers.org/hco/12/GRCh38#107523916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85386144-C-A

107524195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85386548-G-A

107524350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85386693-A-G

107524489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85386821-G-A

107525836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85388188-C-T

107525960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85388319-A-T

107526231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85388565-C-G

107526231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85388565-C-T

107528144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85388821-G-A

107528687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389344-T-A

107528847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389410-G-A

107528847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389410-G-C

107529127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389609-G-C

107529206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389692-A-G

107529223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389707-G-A

107529224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389708-G-A

107529260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389728-A-G

107529381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85389837-A-G

http://identifiers.org/hco/12/GRCh38#107529736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85390150-A-C

http://identifiers.org/hco/12/GRCh38#107529877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85390267-A-C

107529877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85390267-A-G

107529916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85390306-G-T

107530125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85390483-C-T

107530314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85391308-T-A

http://identifiers.org/hco/12/GRCh38#107530394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85391373-C-A

107530441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85391391-T-A

107530612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85391544-C-T

107531018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85391941-G-A

107531018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85391941-G-C

107531043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85391966-C-G

107531121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85392021-G-A

107531121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85392021-G-T

107539901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393338-A-T

107540186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393537-T-A

107540264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393578-A-T

107540330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393631-C-G

107540418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393701-C-T

107540419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393702-C-T

107540465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393748-C-T

http://identifiers.org/hco/12/GRCh38#107540495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85393775-A-C

107540496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393776-G-A

http://identifiers.org/hco/12/GRCh38#107540519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85393799-C-A

107540519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393799-C-T

107540599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85393847-G-A

107543786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397265-C-G

107543787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397266-T-A

107543787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397266-T-C

http://identifiers.org/hco/12/GRCh38#107543858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85397318-C-A

107543872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397332-A-G

107543893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397337-G-A

107543894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397338-T-C

107543894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397338-T-G

107543978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85397412-T-C

http://identifiers.org/hco/12/GRCh38#107544077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#85397511-C-A

107544077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85397511-C-T

107544154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397588-G-T

107544160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397627-C-T

107544215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397671-G-A

107544324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397775-G-A

107544361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397812-G-T

107544423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397875-G-A

107544461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85397911-T-C

107544607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85398052-G-A

107545764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85398556-T-C

107545816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85398608-C-G

107545905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85398681-T-A

107546369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399099-C-T

107546430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399144-C-T

107546460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399166-G-A

107546484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399190-A-G

107547378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399736-T-G

107547412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399769-G-A

107547412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399769-G-T

107547416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85399773-A-G

107547743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85400073-T-C

107548428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85400720-C-G

107548483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85400773-G-A

107548501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85400791-C-G

107548663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85400953-C-G

107548858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85401146-C-T

107548947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85401242-T-C

107549093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85401394-C-G

107549278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85401580-C-T

107549606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85401825-T-C

107549871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85402055-G-A

107550222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85402390-A-T

107550441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85402601-G-A

107550441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85402601-G-T

http://identifiers.org/hco/12/GRCh38#107550463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85402621-C-A

107550487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85402645-G-A

107550487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85402645-G-T

http://identifiers.org/hco/12/GRCh38#107550520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85402698-C-A

107551589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85403692-A-T

107551613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85403716-G-A

107551613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85403716-G-C

107551657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85403762-G-T

107552331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85404505-G-A

http://identifiers.org/hco/12/GRCh38#107552354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85404528-A-C

107552452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85404629-C-T

107552514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85404739-A-G

107552533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85404750-G-A

107552551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85404768-A-G

107552597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85404865-A-G

107552861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405382-C-T

107552880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405411-A-T

107552908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405439-A-G

107552987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405523-G-A

107553044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405580-A-T

107553054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405590-T-C

107554175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405929-G-A

107554175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85405929-G-T

107554306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406118-A-G

107554333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406145-G-A

107554350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406162-T-A

107554381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406193-G-C

107554453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406264-A-G

107554659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406416-G-C

107555170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85406876-T-C

107555340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85407041-C-T

107555391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85407090-A-G

107555397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85407100-G-A

107555620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85407754-G-T

107555648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85407782-G-A

107555933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85408078-C-T

107557528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85410479-T-G

107557629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85410568-A-G

107557758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85410694-C-T

http://identifiers.org/hco/12/GRCh38#107557801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85410739-C-A

http://identifiers.org/hco/12/GRCh38#107558316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85411222-C-A

107558316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85411222-C-T

107558346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85411260-G-A

http://identifiers.org/hco/12/GRCh38#107558425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85411340-C-A

107558631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85411553-G-A

107558631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85411553-G-T

107558809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85411714-C-G

107559091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85411975-G-A

http://identifiers.org/hco/12/GRCh38#107559121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85412001-C-A

107559237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412105-G-C

107559549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412488-T-A

107559549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412488-T-C

107559567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412536-T-C

107559678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412849-A-G

107559712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412878-C-T

107559730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412895-C-T

107559793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412943-T-C

107559800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85412950-C-T

107559882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413041-G-T

107559982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413157-T-C

107560195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413367-C-T

107560358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85413530-A-G

107560360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85413532-G-A

107560394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413575-G-C

107560394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413575-G-T

107560402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413583-C-G

107560569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413712-C-G

107560610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413747-G-C

107560684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413799-T-C

http://identifiers.org/hco/12/GRCh38#107560710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85413814-C-A

107560710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413814-C-T

107560748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413863-G-A

107560752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413867-G-T

107560768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413901-A-G

http://identifiers.org/hco/12/GRCh38#107560797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85413938-C-A

107560802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413943-C-T

107560809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413950-A-G

107560819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413960-G-A

107560882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85413993-T-A

107560893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414004-T-A

107560893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414004-T-C

107560893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414004-T-G

107560896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414006-T-C

107561172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414278-T-A

107561172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414278-T-C

107561257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414359-A-G

107561394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414492-T-C

107562744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414605-C-T

107562902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414735-T-C

107562949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85414777-A-G

107563188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85415023-C-T

107564222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85418551-T-A

107565109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85419385-G-A

107565156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85419436-T-G

http://identifiers.org/hco/12/GRCh38#107565175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85419450-A-C

107565312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85419570-A-T

107565365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85419781-C-T

107565426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85420608-G-A

107565471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85420655-C-T

107565616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85420799-T-A

107565671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85420843-G-A

107565693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85420855-C-T

107565726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85420888-C-T

107565920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421056-A-G

http://identifiers.org/hco/12/GRCh38#107565977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85421101-A-C

107566057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421175-A-G

107566162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421261-T-G

107566339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421430-T-C

107566345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421436-A-G

107566381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421471-T-G

http://identifiers.org/hco/12/GRCh38#107566444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85421528-C-A

107566444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421528-C-T

107566648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85421845-T-C

http://identifiers.org/hco/12/GRCh38#107566684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85421881-C-A

http://identifiers.org/hco/12/GRCh38#107566686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85421883-A-C

107568393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423180-T-C

107568397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423184-G-A

107568493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423267-G-A

107568560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423319-A-G

107568566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423325-A-G

107568600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423359-G-T

107568614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423374-A-G

107568670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423425-C-G

107568729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423481-T-C

107568760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423511-G-T

107568817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423568-A-G

107568907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423656-A-G

107568940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85423688-C-T

107569831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85424899-G-A

107569831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85424899-G-C

107569975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85425038-G-T

107570695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85425592-T-C

107570755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85425653-C-T

107570763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85425661-C-T

107570811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85425709-C-T

107570969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85425864-A-G

107571287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85426192-T-C

107573227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85426520-C-T

107573229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85426522-T-C

107573243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85426536-G-C

107573509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85426856-G-A

107573529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85426876-A-G

http://identifiers.org/hco/12/GRCh38#107573684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85427120-C-A

107573697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85427133-C-G

107574016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85427404-C-G

107574016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85427404-C-T

107574264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85427728-A-G

http://identifiers.org/hco/12/GRCh38#107574285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85427749-C-A

107574285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85427749-C-G

http://identifiers.org/hco/12/GRCh38#107574826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85427994-A-C

107574896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85428057-C-T

107574917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85428076-G-A

107574937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85428096-C-T

107575217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85428365-T-C

107575382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85428507-G-T

107575461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85428585-A-G

107576869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85429667-T-G

107577172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85430293-G-A

107577505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85430524-G-A

107577526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85430545-C-T

107577622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85430626-A-G

107577713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85430708-T-A

107577724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85430718-G-C

107578150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85431369-T-G

107578971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432083-C-T

107579198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432278-C-T

107579274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432346-G-C

http://identifiers.org/hco/12/GRCh38#107579433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85432509-C-A

107579513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432589-G-A

http://identifiers.org/hco/12/GRCh38#107579557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85432647-A-C

107579616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432704-G-A

107579681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432762-T-A

http://identifiers.org/hco/12/GRCh38#107579810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85432813-C-A

107579829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432832-A-G

107579900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85432896-C-G

http://identifiers.org/hco/12/GRCh38#107580505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85433984-C-A

107580505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85433984-C-T

http://identifiers.org/hco/12/GRCh38#107580524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85434004-C-A

107580524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434004-C-G

107580548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434023-G-A

107580549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434024-G-A

107580549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434024-G-T

http://identifiers.org/hco/12/GRCh38#107580640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85434106-C-A

107580640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434106-C-T

107580694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85434147-G-A

107580694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85434147-G-T

http://identifiers.org/hco/12/GRCh38#107580709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85434160-C-A

107580709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85434160-C-T

107580749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85434187-A-G

107580805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85434242-T-C

107580852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85434289-T-C

http://identifiers.org/hco/12/GRCh38#107580901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85434338-C-A

107581106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434546-C-G

107581106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434546-C-T

107581128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434566-T-C

107581191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85434628-G-A

107581191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85434628-G-T

107581272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85434709-G-A

107581272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85434709-G-C

107581272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 85434709-G-T

107581323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434801-G-A

107581323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434801-G-C

107581323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434801-G-T

107581375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434889-T-G

107581434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434938-C-T

http://identifiers.org/hco/12/GRCh38#107581436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85434941-C-A

107581436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434941-C-T

107581443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85434948-A-G

107581657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435166-A-G

107581695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435203-G-A

107582121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435620-G-A

107582121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435620-G-T

107582263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435730-A-T

107582379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435815-A-G

107582431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85435861-C-T

107582880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436168-C-T

107582901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436190-G-A

107583012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436301-G-A

http://identifiers.org/hco/12/GRCh38#107583102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85436392-C-A

http://identifiers.org/hco/12/GRCh38#107583169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85436460-A-C

107583169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436460-A-G

107583236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436505-G-A

107583236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436505-G-T

107583272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436542-C-T

107583326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85436566-C-T

107584309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85438215-T-C

107584484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85438423-C-T

http://identifiers.org/hco/12/GRCh38#107584628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85438566-A-C

107584763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85438693-A-G

107584899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85438818-A-T

107584971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85438889-T-A

107585047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85438975-G-C

107585093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439020-T-C

107585145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439075-C-T

107585578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439464-G-A

107585606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439493-C-T

107585760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439636-T-A

107585760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439636-T-C

107585778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439653-G-A

107585820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439689-C-G

107585820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439689-C-T

107585858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85439720-A-G

107586080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440217-G-T

http://identifiers.org/hco/12/GRCh38#107586107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85440244-C-A

107586121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440263-G-A

107586127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440269-A-G

http://identifiers.org/hco/12/GRCh38#107586168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85440283-C-A

107586168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440283-C-T

107586224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440339-A-G

107586372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440471-G-A

107586372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440471-G-C

107586391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440489-C-T

107586585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440692-G-A

107586598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440705-T-C

107586607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440714-G-A

107586672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440778-G-A

107586753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440862-T-C

107586855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85440963-T-C

107586913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85441009-T-C

107586956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85441047-T-A

107586989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85441080-G-A

107587305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85441209-T-A

107587331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85441235-G-C

107587422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85441328-A-G

107587731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442426-C-T

107587774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442472-A-G

107587802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442500-G-A

107587802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442500-G-T

http://identifiers.org/hco/12/GRCh38#107587975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85442665-C-A

107588070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442747-A-T

107588188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442848-T-C

107588359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442916-T-C

107588392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442945-G-A

107588423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85442975-A-G

107588664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443020-G-T

107588667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443023-C-T

107588946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443217-G-A

107589390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443519-G-A

107589624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443704-A-G

107589800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443883-G-A

107589814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85443897-C-T

107590607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85444583-A-G

107590620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85444596-C-T

http://identifiers.org/hco/12/GRCh38#107590685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85444661-A-C

107590702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85444678-T-A

107590702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85444678-T-C

107590844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85444829-A-G

107591166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85445154-C-T

http://identifiers.org/hco/12/GRCh38#107591208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85445192-A-C

107591208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85445192-A-G

107591660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85445219-G-A

107591951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85445891-T-A

http://identifiers.org/hco/12/GRCh38#107592130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85446034-C-A

107592674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85446928-T-C

107593267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85448342-G-A

107593453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85448494-G-A

107593548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85448575-A-G

107593620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85448645-T-C

http://identifiers.org/hco/12/GRCh38#107593622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85448647-A-C

107593992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85448996-T-C

107594275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85449294-T-G

107594810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85449916-C-G

http://identifiers.org/hco/12/GRCh38#107594899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85450002-A-C

107594940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450032-G-A

107594940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450032-G-C

107595061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450175-G-A

107595067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450182-G-T

107595099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450214-T-C

107595099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450214-T-G

107595130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450232-T-C

107595140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450242-A-G

107595187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450272-C-G

107595187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450272-C-T

107595207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450291-T-A

107595333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450415-C-T

107595464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450547-G-A

107595464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450547-G-T

107595474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450556-C-T

107595529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85450611-T-C

http://identifiers.org/hco/12/GRCh38#107599984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85451117-C-A

107600165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451285-T-C

107600175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451295-T-C

107600255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451368-C-T

107600293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451405-A-G

107600414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451518-T-C

107600550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451656-C-T

http://identifiers.org/hco/12/GRCh38#107600559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85451665-C-A

107600571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451672-G-A

107600571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451672-G-C

107600571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451672-G-T

107600889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85451968-C-G

107600959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85452037-G-A

107602356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85452834-T-A

107602699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453406-C-T

107602749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453455-C-T

107602814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453518-A-G

107602831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453535-C-G

107602831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453535-C-T

107602889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453579-G-A

107602894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453584-T-C

107602926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453616-G-A

107602951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453642-G-A

107603055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453743-T-A

107603124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453812-T-C

107603183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453866-C-G

107603222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85453901-C-T

http://identifiers.org/hco/12/GRCh38#107603372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85454041-C-A

107603501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85454288-G-A

107605595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85457079-C-T

107605625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85457111-G-T

107605772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85457245-G-C

107606038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85457491-C-T

107606211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85457667-A-G

107607408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85459235-C-G

107607408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85459235-C-T

http://identifiers.org/hco/12/GRCh38#107609648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85460014-C-A

107609648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85460014-C-T

107609760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85460127-T-C

107610066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460619-A-G

http://identifiers.org/hco/12/GRCh38#107610102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85460654-C-A

107610102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460654-C-T

107610103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460655-A-G

107610103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460655-A-T

107610116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460668-G-A

107610116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460668-G-C

http://identifiers.org/hco/12/GRCh38#107610124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85460686-C-A

107610124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460686-C-T

http://identifiers.org/hco/12/GRCh38#107610141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85460703-C-A

107610141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460703-C-T

107610398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460963-T-C

107610398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85460963-T-G

http://identifiers.org/hco/12/GRCh38#107610487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85461111-C-A

107610494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461118-G-A

107610494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461118-G-T

http://identifiers.org/hco/12/GRCh38#107610545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85461164-A-C

107610545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461164-A-T

107610697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461317-T-C

107610956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461566-A-G

107611019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461629-G-C

107611030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85461640-A-G

107611813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85462114-G-C

107612004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85462306-G-C

http://identifiers.org/hco/12/GRCh38#107612032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85462334-C-A

107612109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85462409-C-T

107612115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85462415-T-G

http://identifiers.org/hco/12/GRCh38#107612133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85462433-A-C

107612474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85462769-C-T

http://identifiers.org/hco/12/GRCh38#107612694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85462980-C-A

107612880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85463161-A-G

107613015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85463234-T-A

107613157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85463376-C-T

http://identifiers.org/hco/12/GRCh38#107613442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85463617-C-A

107613604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85463741-A-G

107613769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85463907-G-A

107613921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464063-G-A

107614153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464253-T-C

107614155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464254-A-G

107614300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464387-A-G

107614482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464555-T-G

http://identifiers.org/hco/12/GRCh38#107614583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85464649-C-A

http://identifiers.org/hco/12/GRCh38#107614672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85464725-C-A

107614672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464725-C-T

http://identifiers.org/hco/12/GRCh38#107614964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85464978-C-A

107614964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464978-C-T

107614980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464994-G-A

107614980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85464994-G-T

107615218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85465234-A-G

107615639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85465657-G-A

107616022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85465960-A-G

107616214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466125-G-A

107616263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466174-A-G

107616551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466416-C-T

http://identifiers.org/hco/12/GRCh38#107616975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85466845-C-A

107616975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466845-C-T

107617042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466893-A-G

107617062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466925-G-A

107617062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85466925-G-T

107617247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85467103-G-A

107617269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85467125-C-G

107617574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85467427-G-T

107617613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85467472-A-G

107617613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85467472-A-T

http://identifiers.org/hco/12/GRCh38#107617638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85467497-C-A

107617779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85467632-G-A

107617779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85467632-G-T

http://identifiers.org/hco/12/GRCh38#107617809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85467662-C-A

107617850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85467694-G-A

107617850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85467694-G-C

107617850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85467694-G-T

http://identifiers.org/hco/12/GRCh38#107618393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85468188-C-A

107618393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85468188-C-T

107618500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85468252-G-A

107618500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85468252-G-T

http://identifiers.org/hco/12/GRCh38#107618513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85468268-A-C

http://identifiers.org/hco/12/GRCh38#107618521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85468276-C-A

107618731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85468473-G-C

107618731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85468473-G-T

107618869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85468609-C-T

107619343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469019-G-C

107619581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469196-C-G

107619669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469273-A-G

107619907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469466-G-A

107619907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469466-G-C

107619907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469466-G-T

http://identifiers.org/hco/12/GRCh38#107619970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85469528-C-A

http://identifiers.org/hco/12/GRCh38#107620210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85469811-C-A

107620210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469811-C-T

107620223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469823-G-T

http://identifiers.org/hco/12/GRCh38#107620231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85469831-C-A

107620231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469831-C-T

107620270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469868-T-C

107620312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85469917-A-G

107620502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85470123-G-A

107620548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85470165-G-A

107621302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85471644-C-T

107621303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85471645-G-A

107621432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85471789-C-T

107621551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85471899-C-T

107621588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85471948-G-A

107621588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85471948-G-T

107621795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85472106-A-G

107622132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85472387-T-C

107626738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473300-G-A

107626828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473392-T-C

http://identifiers.org/hco/12/GRCh38#107627106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85473505-A-C

107627279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473707-C-T

107627406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473861-G-C

107627421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473876-G-A

107627458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473913-C-G

107627470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473925-G-A

107627470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85473925-G-C

107627632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85474113-T-C

107634052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85474734-T-C

107634713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85475817-T-G

107634865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85475975-A-G

107634865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85475975-A-T

107634913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85475999-T-G

107634914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 85476002-T-G

107635004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85476086-A-G

107635031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85476114-T-C

107635146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85476249-G-A

107635146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85476249-G-T

107635185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476270-T-C

107635207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476292-G-A

107635207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476292-G-T

http://identifiers.org/hco/12/GRCh38#107635239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476325-C-A

107635239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476325-C-T

http://identifiers.org/hco/12/GRCh38#107635243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476329-C-A

107635243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476329-C-T

107635247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476333-A-G

107635255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476341-G-A

http://identifiers.org/hco/12/GRCh38#107635265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476349-C-A

107635265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476349-C-T

107635335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 85476417-G-C

http://identifiers.org/hco/12/GRCh38#107635404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476485-C-A

http://identifiers.org/hco/12/GRCh38#107635422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476503-C-A

http://identifiers.org/hco/12/GRCh38#107635472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476547-A-C

http://identifiers.org/hco/12/GRCh38#107635498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476578-A-C

http://identifiers.org/hco/12/GRCh38#107635540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#85476621-C-A

107635540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85476621-C-T

http://identifiers.org/hco/12/GRCh38#107635740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85477414-C-A

107635811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477484-G-A

http://identifiers.org/hco/12/GRCh38#107635829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85477502-A-C

107635829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477502-A-T

http://identifiers.org/hco/12/GRCh38#107635857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85477533-C-A

107635857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477533-C-G

107635857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477533-C-T

107635893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477586-C-G

107636055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477952-C-T

107636086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85477969-T-A

107636352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85478209-G-T

107636514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85478360-G-A

107636698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85478545-G-A

107636790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85478625-G-C

107636917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85478759-G-T

http://identifiers.org/hco/12/GRCh38#107639653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85480300-C-A

107639653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85480300-C-T

107639681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85480328-G-C

107639796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85480423-T-C

107640282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481329-G-A

107640282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481329-G-T

107640298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481339-T-C

107640298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481339-T-G

107640342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85481383-T-A

107640342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85481383-T-C

107640456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481497-G-A

107640456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481497-G-T

107640461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481502-T-C

http://identifiers.org/hco/12/GRCh38#107640499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85481756-C-A

107640499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481756-C-G

107640500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481757-T-C

107640500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481757-T-G

http://identifiers.org/hco/12/GRCh38#107640504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85481761-C-A

107640504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481761-C-T

107640558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481811-G-A

107640558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481811-G-T

107640626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481852-C-G

107640626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481852-C-T

107640644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481864-G-C

107640644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85481864-G-T

107640829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482039-T-A

107640829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482039-T-C

107640865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482149-G-T

107640924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482186-A-G

107640966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482222-G-A

107641050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482283-C-G

107641050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482283-C-T

http://identifiers.org/hco/12/GRCh38#107641346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85482512-C-A

107641365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482531-G-A

http://identifiers.org/hco/12/GRCh38#107641373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85482547-A-C

107641373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482547-A-G

107641487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482709-T-A

107641508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85482730-C-G

107641786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483339-G-A

107641955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483459-A-G

107642049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483542-T-C

107642049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483542-T-G

107642126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85483612-T-C

107642280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483714-G-A

107642280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483714-G-C

107642280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483714-G-T

107642300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483733-C-T

http://identifiers.org/hco/12/GRCh38#107642301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85483734-C-A

107642301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483734-C-T

http://identifiers.org/hco/12/GRCh38#107642314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85483745-C-A

107642314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483745-C-T

107642317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483748-T-C

107642317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483748-T-G

107642343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483772-C-T

107642525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85483964-A-G

107642669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85484091-C-T

http://identifiers.org/hco/12/GRCh38#107645339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85484570-C-A

107645536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85484711-C-G

107645543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85484718-C-G

http://identifiers.org/hco/12/GRCh38#107645568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85484742-A-C

107645692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85484909-G-A

107645741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85484957-G-A

107645857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85485071-T-C

http://identifiers.org/hco/12/GRCh38#107645888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85485101-C-A

107646079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85485310-C-G

107646079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85485310-C-T

107646080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85485311-G-A

107646350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85485572-A-G

107646372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron_variant, undefined
orthologous variants: 85485594-G-C

107646413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85485651-G-A

107646413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85485651-G-C

107646561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85485807-G-A

107646702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85485950-G-A

107646871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85486240-C-T

107646872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85486241-T-C

107646989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85486331-G-A

107647131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85486458-A-G

107648000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85486818-A-G

107648417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85486896-G-C

107648653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85487139-C-T

107649043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85487379-T-C

107649079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85487412-A-G

http://identifiers.org/hco/12/GRCh38#107649122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85487426-C-A

107649185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85487455-G-C

http://identifiers.org/hco/12/GRCh38#107649339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85487586-C-A

107649339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487586-C-G

107649339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487586-C-T

http://identifiers.org/hco/12/GRCh38#107649346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85487593-C-A

107649346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487593-C-G

107649424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487622-T-C

107649460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487656-A-G

107649480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487676-G-A

107649480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487676-G-T

107649505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487681-G-T

http://identifiers.org/hco/12/GRCh38#107649539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85487708-C-A

107649557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487721-G-T

107649615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487778-G-T

107649653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487803-A-G

107649658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487808-T-C

107649674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 85487824-A-T

http://identifiers.org/hco/12/GRCh38#107651602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85490276-C-A

107651602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490276-C-T

http://identifiers.org/hco/12/GRCh38#107651644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85490313-C-A

107651644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490313-C-T

107651682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85490350-T-G

107651902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490528-G-T

http://identifiers.org/hco/12/GRCh38#107651916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85490541-C-A

107651916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490541-C-T

107651918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490543-T-C

107651924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490549-A-G

107651924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490549-A-T

107651927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490555-G-A

107651927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490555-G-C

107651927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490555-G-T

107652164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85490784-G-A

107654989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85491634-C-T

107655146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85491746-G-T

107655347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85491911-C-T

107655365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85491929-C-G

107655448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492012-C-G

http://identifiers.org/hco/12/GRCh38#107655465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85492029-C-A

107655465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492029-C-T

107655636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492173-C-G

107655669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492204-C-T

107655726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492260-G-A

107655726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492260-G-T

http://identifiers.org/hco/12/GRCh38#107656362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85492713-A-C

107656377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492728-T-C

107656382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492733-G-A

107656409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492760-G-A

107656427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492816-G-A

107656427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85492816-G-C

107656600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85493020-A-G

http://identifiers.org/hco/12/GRCh38#107656811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85493200-C-A

107656811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85493200-C-T

http://identifiers.org/hco/12/GRCh38#107657397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85493916-C-A

107657397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85493916-C-T

http://identifiers.org/hco/12/GRCh38#107657415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85493940-A-C

107657415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: intron variant
orthologous variants: 85493940-A-T

107657532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85494027-A-G

107657589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85494084-A-G

107657625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85494120-G-A

107657625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85494120-G-C

http://identifiers.org/hco/12/GRCh38#107657628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85494123-C-A

107657628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85494123-C-G

107657628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: synonymous variant
orthologous variants: 85494123-C-T

107657823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494321-G-A

107657823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494321-G-T

http://identifiers.org/hco/12/GRCh38#107657882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85494404-C-A

107657884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494406-G-A

107657884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494406-G-T

http://identifiers.org/hco/12/GRCh38#107657993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85494510-C-A

107657993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494510-C-T

107658009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494526-G-T

107658105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494617-T-A

http://identifiers.org/hco/12/GRCh38#107658155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85494667-C-A

107658156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494668-T-A

107658157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494669-G-A

107658157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494669-G-T

107658250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85494761-G-A

107658497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495012-T-C

http://identifiers.org/hco/12/GRCh38#107658506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85495021-C-A

107658595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495114-T-C

107658711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495236-G-A

107658711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495236-G-T

107658719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495244-G-T

107658774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495298-A-G

107659236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495792-G-T

http://identifiers.org/hco/12/GRCh38#107659298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85495856-C-A

107659298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: 85495856-C-T

http://identifiers.org/hco/12/GRCh38#107659327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23844
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85495887-C-A