http://identifiers.org/hco/6/GRCh38#13357864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43348750-C-A

13357864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348750-C-T

13357919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348815-G-T

13357926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348821-A-G

13357974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348865-T-C

http://identifiers.org/hco/6/GRCh38#13357975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43348866-C-A

13358020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348910-G-A

13358020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348910-G-T

13358047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43348924-A-G

http://identifiers.org/hco/6/GRCh38#13358576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43349427-C-A

13358576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349427-C-T

13358688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349531-G-A

13358688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349531-G-T

13358694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349537-G-T

13358719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349562-A-G

13358719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349562-A-T

http://identifiers.org/hco/6/GRCh38#13358818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43349648-C-A

13358871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349700-G-T

13358911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349755-G-T

13358917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349761-A-G

http://identifiers.org/hco/6/GRCh38#13358943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43349788-C-A

13358979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349824-G-A

http://identifiers.org/hco/6/GRCh38#13359101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43349906-C-A

13359162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349945-A-G

13359179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43349962-T-C

http://identifiers.org/hco/6/GRCh38#13359356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43350095-C-A

13359412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350153-A-G

13359438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350179-T-C

13359490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350231-A-G

13359644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350348-T-C

13360577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350724-G-C

13360577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350724-G-T

13360780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350885-G-A

13360780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350885-G-T

13360833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350942-G-C

13360833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43350942-G-T

13361082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351102-A-G

13361126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351122-C-T

13361297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351283-T-C

13361311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351299-G-T

http://identifiers.org/hco/6/GRCh38#13361316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43351304-A-C

http://identifiers.org/hco/6/GRCh38#13361318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43351306-C-A

13361318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351306-C-T

http://identifiers.org/hco/6/GRCh38#13361334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43351340-C-A

13361378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351409-G-A

13361378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351409-G-T

13361580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351507-A-G

13361634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351561-G-T

13361649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351576-A-G

http://identifiers.org/hco/6/GRCh38#13361664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43351591-C-A

13361664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351591-C-T

13361860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351743-G-A

13361860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351743-G-T

13361910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351792-T-C

13361921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43351803-T-C

http://identifiers.org/hco/6/GRCh38#13362053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43351900-C-A

http://identifiers.org/hco/6/GRCh38#13362152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43351973-C-A

http://identifiers.org/hco/6/GRCh38#13363056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43352327-C-A

13363195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43352451-G-T

13363561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43352780-T-G

http://identifiers.org/hco/6/GRCh38#13363601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43352804-C-A

13363601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43352804-C-G

13363601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43352804-C-T

13363644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43352850-A-G

13363987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353140-G-A

13363987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353140-G-T

13363994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353147-C-T

13363995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353148-T-C

13363995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353148-T-G

13364088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353180-G-A

http://identifiers.org/hco/6/GRCh38#13364115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43353199-C-A

http://identifiers.org/hco/6/GRCh38#13364240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43353308-A-C

13364240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353308-A-G

13364270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353358-A-T

13364423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353507-G-A

13364423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353507-G-C

13364423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353507-G-T

13364569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353636-G-T

13364589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353656-G-A

13364589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353656-G-T

http://identifiers.org/hco/6/GRCh38#13364630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43353693-C-A

13364630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353693-C-T

http://identifiers.org/hco/6/GRCh38#13364658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43353721-C-A

http://identifiers.org/hco/6/GRCh38#13364703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43353766-C-A

13364703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353766-C-T

13364737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3 prime UTR variant
orthologous variants: 43353795-T-G

13364827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43353885-G-A

13364830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43353888-A-G

13365010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354068-G-A

13365055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: missense variant
orthologous variants: 43354113-G-T

13365103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354161-G-A

13365103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: missense variant
orthologous variants: 43354161-G-T

13365127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354185-G-A

13365136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354194-G-A

13365136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354194-G-C

13365157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354215-G-A

13365217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354275-G-A

http://identifiers.org/hco/6/GRCh38#13365298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43354356-A-C

13365298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354356-A-G

13365373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354431-G-A

13365391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354449-G-A

13365391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354449-G-C

13365391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354449-G-T

13365439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: missense variant
orthologous variants: 43354497-C-G

13365439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354497-C-T

13365492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: missense variant
orthologous variants: 43354550-C-T

13365499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: synonymous variant
orthologous variants: 43354557-G-A

http://identifiers.org/hco/6/GRCh38#13365631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43354689-C-A

13365631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 43354689-C-G

13365631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 43354689-C-T

13365661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 43354719-G-T

13368162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43354867-A-G

13368204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43354904-C-G

13368204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43354904-C-T

13368205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43354905-G-A

13368262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43354961-C-T

http://identifiers.org/hco/6/GRCh38#13368421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43355097-C-A

13368421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43355097-C-G

13368510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43355155-T-C

http://identifiers.org/hco/6/GRCh38#13368571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43355211-C-A

13368762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43355369-T-C

13369828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356109-G-A

13369828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356109-G-T

13369896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356165-G-T

13369897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356166-G-A

13371450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356537-C-T

13371521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356601-C-G

13371572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356656-T-C

13371572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356656-T-G

13371711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356795-T-C

13371712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356796-G-C

13371712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356796-G-T

13371909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43356968-G-A

13372459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43357446-C-T

13372571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43357568-C-T

13372731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43357677-C-T

13372832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43357778-G-A

13373403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43358330-C-T

http://identifiers.org/hco/6/GRCh38#13375309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43359746-C-A

13375558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43359992-C-T

13375679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43360108-C-G

13375683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43360112-C-T

13375909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43360928-T-A

13375909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43360928-T-C

13375960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43360961-T-C

13376000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43361001-G-A

http://identifiers.org/hco/6/GRCh38#13377072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43362338-C-A

13377072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43362338-C-T

13377104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43362370-T-C

13377106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43362372-T-C

13377553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43362763-G-A

13377592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43362798-G-C

13377988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363212-G-A

13378126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363290-C-T

13378128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363292-T-C

13378135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363299-C-T

http://identifiers.org/hco/6/GRCh38#13378136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43363300-A-C

13378191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363357-A-T

13378269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363456-G-A

13378269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363456-G-C

13378304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363527-C-T

13378358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363691-C-G

13378494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363824-C-T

13378646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363961-G-A

13378688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43363995-G-T

13379017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43364291-G-C

13379242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43364459-G-A

http://identifiers.org/hco/6/GRCh38#13379880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43365682-A-C

http://identifiers.org/hco/6/GRCh38#13380048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43365844-A-C

13380107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43365902-G-A

13380107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43365902-G-C

13380167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43365962-A-T

13380768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43366328-T-A

13380768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43366328-T-C

13380935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43366685-C-T

http://identifiers.org/hco/6/GRCh38#13380994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#43366744-A-C

13380994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43366744-A-G

13381058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43366777-G-A

13381111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43366826-T-C

13381378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43367062-A-G

13381406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43367444-T-C

http://identifiers.org/hco/6/GRCh38#13381409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43367447-A-C

13381409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43367447-A-T

13381576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43367605-C-G

13381615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43367643-C-T

http://identifiers.org/hco/6/GRCh38#13381798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43367822-C-A

13381798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43367822-C-T

13384544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368138-G-C

13384584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368176-T-C

http://identifiers.org/hco/6/GRCh38#13384585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43368177-A-C

http://identifiers.org/hco/6/GRCh38#13384780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43368374-C-A

13384809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368405-G-C

13384819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368412-G-A

13384888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368481-C-G

13384888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368481-C-T

13385175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368758-G-A

13385231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368816-T-C

13385337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43368905-T-A

13385489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43369104-G-T

13385529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43369149-T-A

13385722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43369315-T-G

13385777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43369391-A-G

13395584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43370679-G-C

13395608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43370705-T-C

13395718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43370794-A-G

13395776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43370867-C-T

13396275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43371011-A-G

13396331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43371071-A-G

13397662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43372468-G-A

13397765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43372571-C-T

13398459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43375564-C-T

13400183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43379014-G-A

13400421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43379215-G-C

13401093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43379835-C-T

13401684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43380213-T-G

13401736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43380259-A-G

13401759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43380282-C-G

13401864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43380410-A-G

13402021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43380554-T-C

13402229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381017-A-G

13402259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381046-T-G

13402283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381069-G-A

13402288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381074-C-T

13402380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381236-T-C

13402577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381407-T-A

13402598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381426-A-G

13402655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381482-A-G

13402820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381638-A-G

13402907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43381726-G-C

13404081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43382621-A-G

13404224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43382833-G-T

13404399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383052-T-A

13404415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383066-G-A

13404418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383069-T-C

13404442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383093-G-A

13405435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383287-G-A

13405435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383287-G-C

13405435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383287-G-T

13405534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383373-G-A

13405599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383428-A-G

13405921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383692-A-G

13405957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383725-C-T

13405965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43383733-A-G

13406413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43384136-G-C

13406530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43384246-C-T

13406588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43384289-C-T

13406773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43384445-G-A

13406856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43384517-A-G

13407724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43385350-G-C

13407771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43385399-A-T

13407871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43385499-G-T

13407931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43385562-A-G

13408064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43385701-G-A

13408145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43385784-T-A

13408145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43385784-T-C

http://identifiers.org/hco/6/GRCh38#13408251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43385887-C-A

13408251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43385887-C-T

13408358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43385994-A-G

13408477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43386127-G-A

13408525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43386176-G-A

13408633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43386285-C-T

13408743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43386376-A-G

13410038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43386886-T-G

13410940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43387415-T-A

13412838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43387979-A-G

13412939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388084-T-C

13413139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388295-C-T

13413152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388306-C-T

http://identifiers.org/hco/6/GRCh38#13413192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43388351-C-A

13413203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388362-G-C

13413384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388519-G-A

13413553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388691-G-A

13413553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388691-G-C

http://identifiers.org/hco/6/GRCh38#13413582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43388720-C-A

http://identifiers.org/hco/6/GRCh38#13413671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43388801-C-A

13413671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388801-C-T

13413779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43388907-G-C

13413792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43388920-G-C

13413891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43389047-T-C

13417603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43390160-G-T

13417660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43390215-T-C

http://identifiers.org/hco/6/GRCh38#13417879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43390424-C-A

13418334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43390912-C-T

13418483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391053-C-T

13418773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391334-G-A

13418782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391343-C-T

http://identifiers.org/hco/6/GRCh38#13418788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43391348-C-A

13418990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391491-T-C

13418999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391500-C-T

13419125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391621-C-T

13419126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391622-A-G

13419438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391932-G-A

13419446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43391942-C-T

13420247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393058-C-T

13420647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393397-G-A

13420714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393439-G-T

13420808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393528-A-T

13421566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393876-T-C

13421585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393893-C-T

13421656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43393964-G-A

13422224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43395307-A-G

13422332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43395581-G-T

13422376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43395623-T-C

13422663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43395905-C-G

13422665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43395907-G-A

13422728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43395969-T-C

13422953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396211-T-A

13422977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396236-T-C

13423054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396313-G-A

13423181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396406-A-G

13423213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396438-C-T

13423374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396652-C-T

13423508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396803-T-G

13423635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396935-T-C

13423663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396959-T-G

13423698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43396995-G-C

13423810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43397103-G-A

13425466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43397352-G-A

13425512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43397398-A-G

13425531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43397417-G-A

13426127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43397775-C-T

13426336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43397964-C-T

13426505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43398168-G-A

13426506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43398169-T-C

http://identifiers.org/hco/6/GRCh38#13426544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43398202-C-A

13426546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43398204-C-T

13426646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43398373-T-C

13426936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43398629-G-A

13427042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43398726-A-G

13427721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399312-T-C

13427803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399387-C-T

13427822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399409-G-A

13427828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399415-G-C

13427987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399571-G-A

13427987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399571-G-T

13428072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399654-C-G

13428072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43399654-C-T

13428404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43400461-C-T

13428752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43401182-A-T

13429007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43401434-G-C

13429056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43401482-G-A

13431921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403658-A-G

13431970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403709-C-T

13431987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403725-T-G

13432018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403756-G-A

13432039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403780-C-G

13432039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403780-C-T

http://identifiers.org/hco/6/GRCh38#13432050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43403791-C-A

13432050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403791-C-T

13432451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43403936-T-G

13432649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43404097-C-T

13432691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43404142-C-T

13432739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43404182-T-C

13432801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43404250-T-C

13433986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43404997-G-A

http://identifiers.org/hco/6/GRCh38#13434415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43405088-C-A

13434474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43405147-G-A

http://identifiers.org/hco/6/GRCh38#13434708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43405209-A-C

13434896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43405572-G-T

13436504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43406428-A-G

http://identifiers.org/hco/6/GRCh38#13436881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43406803-A-C

13437060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43406977-A-T

13437208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43407050-T-C

13437519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43407256-C-T

http://identifiers.org/hco/6/GRCh38#13437618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43407348-C-A

13439228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43408158-A-G

http://identifiers.org/hco/6/GRCh38#13439313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43408235-A-C

13439705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43408529-T-C

13440524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43409550-C-T

13440553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43409579-T-C

http://identifiers.org/hco/6/GRCh38#13440559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43409614-C-A

13440559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43409614-C-G

13440630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43409675-C-G

13440761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43409844-C-T

13445150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411433-C-T

13445153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411436-G-A

13445187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411468-G-A

13445279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411570-A-T

13445326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411614-T-C

13445394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411684-G-C

13445420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43411710-C-T

13445794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43412060-A-G

13445795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43412061-T-G

13446084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43412461-C-G

13446214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43412591-G-T

http://identifiers.org/hco/6/GRCh38#13446225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43412602-A-C

13446225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43412602-A-G

13446886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414410-C-T

13446919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414443-C-G

13446957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414481-T-C

13447001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414516-T-A

13447085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414607-C-T

13447108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414630-G-A

13447187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43414682-G-C

http://identifiers.org/hco/6/GRCh38#13448579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43415823-C-A

13448579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43415823-C-G

13448625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43415869-C-G

13448717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43415979-T-C

13450535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43417267-C-T

13450607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43417333-A-T

13450629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43417355-T-C

13450785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43417510-G-A

http://identifiers.org/hco/6/GRCh38#13451092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43417719-C-A

13451092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43417719-C-G

13451170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43417810-C-T

13451357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43418266-C-T

13451358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43418267-G-A

13451524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43418439-C-T

13453277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43418787-T-C

13453300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43418807-C-G

13453429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43418934-G-A

13454570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43421386-A-G

13454685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43421501-C-T

13454852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43421657-T-C

13454852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43421657-T-G

13454900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, undefined
orthologous variants: 43421680-C-T

13455034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43421814-G-C

13455083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43421855-C-T

13455104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43421859-C-T

13455473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43422243-C-T

13456561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43424564-G-A

13456574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43424577-C-G

13456712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43424670-G-A

13456993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43424918-G-T

13456996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43424921-G-A

13457134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425115-G-A

13457274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425245-G-A

13457315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425290-T-G

13457319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425294-G-T

13457389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425368-G-T

13457541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425499-G-A

13457561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425518-G-A

13457784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425686-G-C

13457804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43425706-G-A

13461837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43426018-C-T

13461876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43426057-G-A

13461878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43426059-C-T

13461904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43426087-G-A

13462810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43427109-A-G

13462956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43427478-C-T

13463060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43427585-C-G

13463118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43427634-T-C

13463529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428002-T-A

13463675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428114-C-T

http://identifiers.org/hco/6/GRCh38#13463782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43428174-C-A

13464180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428370-G-A

13464256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428444-G-C

13464318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428492-G-T

13464440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428627-C-T

13464644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428846-G-C

13464677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43428877-T-C

http://identifiers.org/hco/6/GRCh38#13464908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43429252-A-C

13464908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43429252-A-G

13464989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43429329-C-T

13465551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43430271-T-A

13465610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43430348-G-C

13466518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43438554-G-A

13466518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43438554-G-C

13466725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43438723-T-C

13466827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43438832-C-T

13467130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43439105-T-A

13467303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43439266-C-T

13467381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43439334-G-A

13467408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43439358-C-G

13467853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43440304-A-G

13467897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43440359-G-A

13467900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43440363-T-C

13467976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43440437-G-A

http://identifiers.org/hco/6/GRCh38#13468265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43441286-C-A

13468338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43441371-T-A

13468498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43441508-C-T

13468526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43441537-G-A

13468760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43441793-A-G

13468826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43441851-T-C

13469004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442029-C-T

13469055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442078-A-T

13469169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442224-A-G

13469174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442228-A-G

http://identifiers.org/hco/6/GRCh38#13469219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43442272-C-A

13469219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442272-C-T

http://identifiers.org/hco/6/GRCh38#13469221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43442274-C-A

13469221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442274-C-G

13469221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron variant
orthologous variants: 43442274-C-T

13469285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43442340-A-T

http://identifiers.org/hco/6/GRCh38#13469309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43442364-C-A

http://identifiers.org/hco/6/GRCh38#13470286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43442688-C-A

13470286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43442688-C-T

13470302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43442704-G-A

13470302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43442704-G-T

13470412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43442816-G-A

13470412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43442816-G-C

13470443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43442847-A-G

13470507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43442913-G-A

13470582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43442981-T-C

13470621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43443019-T-C

http://identifiers.org/hco/6/GRCh38#13470686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43443082-C-A

13470710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443101-T-G

13470729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443118-G-A

13470729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443118-G-C

13470729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443118-G-T

http://identifiers.org/hco/6/GRCh38#13470763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43443153-A-C

13470769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443159-A-G

13470805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443195-G-C

13470847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443237-G-T

13471018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43443572-G-A

http://identifiers.org/hco/6/GRCh38#13471477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43444285-C-A

13471660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43444457-T-C

13471675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43444476-C-T

13473561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43444913-A-G

13479465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43449260-A-G

13479465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43449260-A-T

13480262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450020-G-A

13480363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450123-G-A

13480431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450189-C-T

http://identifiers.org/hco/6/GRCh38#13480979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43450454-C-A

13481016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450490-G-T

13481249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450687-C-G

13481249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450687-C-T

http://identifiers.org/hco/6/GRCh38#13481260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43450698-A-C

http://identifiers.org/hco/6/GRCh38#13481263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43450701-C-A

13481263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450701-C-T

13481292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450726-G-C

13481318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43450820-G-C

http://identifiers.org/hco/6/GRCh38#13481797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43451415-A-C

13481804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43451422-C-T

13481855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43451477-A-G

13481892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43451512-T-G

13482459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452245-C-G

13482459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452245-C-T

13482466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452254-G-T

13482467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452255-C-T

13482473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452261-G-A

13483318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452907-T-C

13483323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452971-A-G

13483329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452977-G-A

13483329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43452977-G-C

13483405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43453165-A-T

13483409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43453169-G-A

13483517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43453274-A-G

13483527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43453284-T-C

13483882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43453615-T-C

13483884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43453617-T-C

13484279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43454430-A-T

13484941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43455491-T-C

13484980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43455531-T-C

13485820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43456035-G-A

13485830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43456045-C-T

http://identifiers.org/hco/6/GRCh38#13486281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43456428-C-A

13486281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43456428-C-T

13486377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43456516-G-A

13486377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43456516-G-C

13486377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43456516-G-T

http://identifiers.org/hco/6/GRCh38#13486385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#43456524-C-A

13486385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43456524-C-G

13486385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43456524-C-T

13486386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43456525-A-G

13486386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43456525-A-T

13486492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43456624-G-A

13486492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43456624-G-T

13486520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43456653-G-A

13486520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43456653-G-T

13486946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457029-C-T

13486964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457047-C-G

http://identifiers.org/hco/6/GRCh38#13487005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43457090-C-A

13487005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457090-C-T

13487016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457101-G-A

13487016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457101-G-C

13487016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457101-G-T

13487076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457168-G-A

13487076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457168-G-C

13487076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457168-G-T

13487135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43457227-G-A

13487135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 43457227-G-T

http://identifiers.org/hco/6/GRCh38#13487159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43457251-A-C

13487159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457251-A-G

13487214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457306-G-A

13487214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457306-G-C

http://identifiers.org/hco/6/GRCh38#13487232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43457324-C-A

13487232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457324-C-G

13487232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457324-C-T

13487239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457331-C-T

http://identifiers.org/hco/6/GRCh38#13487487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#43457517-C-A

13487487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21096
most severe consequence: 5 prime UTR variant
orthologous variants: 43457517-C-G