3249449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130548265-G-T

3249634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130548446-G-A

http://identifiers.org/hco/20/GRCh38#3249912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130548703-C-A

http://identifiers.org/hco/20/GRCh38#3250046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130548802-C-A

3250084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130548838-T-C

http://identifiers.org/hco/20/GRCh38#3250260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130549000-A-C

3250260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549000-A-G

3250289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549048-G-A

3250289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549048-G-C

3250555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549256-G-A

3250555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549256-G-T

3250934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549636-T-C

3251100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130549945-T-C

http://identifiers.org/hco/20/GRCh38#3251202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130550047-C-A

3251202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550047-C-G

3251202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550047-C-T

3251507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550334-G-A

http://identifiers.org/hco/20/GRCh38#3251706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130550499-C-A

3251706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550499-C-T

http://identifiers.org/hco/20/GRCh38#3251808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130550595-C-A

3251896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550682-A-G

3251923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550709-A-G

http://identifiers.org/hco/20/GRCh38#3252221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130550808-C-A

3252221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550808-C-T

3252248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550826-G-A

3252280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550867-T-A

3252280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130550867-T-C

3252443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130551012-G-A

3252443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3 prime UTR variant
orthologous variants: 130551012-G-T

3252647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130551201-G-T

3252690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130551244-A-G

3252690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130551244-A-T

3252732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551286-G-A

3252732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551286-G-T

3252755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551356-T-G

3252756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551357-G-A

3252756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551357-G-T

3252764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551365-G-A

3252764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551365-G-T

http://identifiers.org/hco/20/GRCh38#3252794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130551405-C-A

3252797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551408-G-A

3252797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551408-G-C

3252797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551408-G-T

http://identifiers.org/hco/20/GRCh38#3252799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130551410-C-A

3252799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551410-C-T

3253643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551786-G-A

3253643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551786-G-T

3253712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130551843-T-C

3255169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552690-C-T

http://identifiers.org/hco/20/GRCh38#3255186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130552701-C-A

3255186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552701-C-T

3255211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130552724-G-A

3255211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130552724-G-T

3255294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552807-T-A

3255294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552807-T-C

3255295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552808-G-A

3255295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552808-G-T

http://identifiers.org/hco/20/GRCh38#3255316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130552827-C-A

3255316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552827-C-T

3255432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552953-T-A

3255432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552953-T-C

http://identifiers.org/hco/20/GRCh38#3255436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130552957-C-A

3255436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130552957-C-T

http://identifiers.org/hco/20/GRCh38#3255567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130553082-C-A

3255567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130553082-C-G

3255668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130553330-T-G

3255744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130553413-A-G

3255815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554008-G-A

http://identifiers.org/hco/20/GRCh38#3255865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130554056-C-A

3255865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554056-C-T

3255941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554133-G-A

3255941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554133-G-C

3255941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554133-G-T

3255972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554148-T-C

3256081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130554255-C-G

3256081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130554255-C-T

3256132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130554303-T-G

3256237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554406-C-T

3256344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554475-G-T

3259445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554847-T-C

3259445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130554847-T-G

http://identifiers.org/hco/20/GRCh38#3259490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130554882-C-A

3259490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130554882-C-T

3259615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555007-G-T

3259634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555026-G-A

3259645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555037-G-T

3259647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555039-A-T

3259894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555265-T-A

3259894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555265-T-C

3259894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555265-T-G

3259903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555298-C-T

3259947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130555342-C-T

3259961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130555356-G-A

3260050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130555445-T-C

3260629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130556389-T-A

3260828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130556490-T-C

3260875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130556557-G-T

3261104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130556809-T-C

3261214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130556924-T-C

3261393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130557110-G-T

3263477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130557536-T-C

http://identifiers.org/hco/20/GRCh38#3263686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130558554-A-C

3263722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130558590-T-A

3263727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130558595-T-C

3263745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130558613-C-T

3264088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130558904-G-A

http://identifiers.org/hco/20/GRCh38#3264303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130559061-C-A

3264303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559061-C-T

3264318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559076-T-C

http://identifiers.org/hco/20/GRCh38#3264338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130559096-C-A

3264338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559096-C-G

3264338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559096-C-T

3264384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559137-T-A

3264384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559137-T-C

3264388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559141-T-A

3264414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559157-T-C

3264443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130559186-A-G

3264451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130559194-T-C

3264455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130559198-A-G

3264488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130559231-A-G

http://identifiers.org/hco/20/GRCh38#3264536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130559277-C-A

3264536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559277-C-G

3264536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559277-C-T

3264565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559306-G-A

3264565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130559306-G-T

3268366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130560591-G-A

3268366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130560591-G-T

http://identifiers.org/hco/20/GRCh38#3268373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130560604-A-C

3268373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130560604-A-T

3268441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130560656-G-C

3268489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130560703-C-T

3270331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561683-T-C

3270331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561683-T-G

3270341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561693-G-A

3270341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561693-G-C

3270341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561693-G-T

3270371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561720-A-T

http://identifiers.org/hco/20/GRCh38#3270372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130561721-C-A

3270372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561721-C-G

3270372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561721-C-T

3270517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130561850-C-T

3270625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130561960-A-T

http://identifiers.org/hco/20/GRCh38#3270699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130562016-A-C

3270782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130562185-C-T

http://identifiers.org/hco/20/GRCh38#3270794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130562197-A-C

http://identifiers.org/hco/20/GRCh38#3270801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130562206-A-C

3270969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130562394-T-C

3270973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130562398-T-C

3271127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130562841-A-G

http://identifiers.org/hco/20/GRCh38#3271188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130562902-A-C

3271390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130563064-G-A

3271408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130563082-G-T

3271624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130563276-T-A

3271739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130563380-A-G

3271742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130563383-C-T

3275373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130565316-T-C

3275582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130565523-G-A

3275646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130565587-A-G

3276076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130566010-C-T

3276234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130566184-A-G

3276406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130566303-C-T

3277124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130567516-G-A

3277124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130567516-G-C

3277371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130567773-C-T

3277382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130567785-C-T

3277607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130567999-C-T

3277933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130568542-G-A

3278749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130568912-G-C

3278871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130569027-C-T

3278897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130569053-A-G

3278905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130569061-T-C

3279005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130569152-G-C

3279005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130569152-G-T

3279253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130569375-G-T

3280059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130571042-G-A

http://identifiers.org/hco/20/GRCh38#3280163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130571129-C-A

http://identifiers.org/hco/20/GRCh38#3280183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130571151-C-A

3280183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130571151-C-T

3280188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130571156-G-A

http://identifiers.org/hco/20/GRCh38#3280968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572055-C-A

3280991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572077-T-C

3281119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572160-C-T

http://identifiers.org/hco/20/GRCh38#3281277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572301-C-A

3281277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572301-C-T

3281306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572329-G-A

http://identifiers.org/hco/20/GRCh38#3281429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572538-A-C

http://identifiers.org/hco/20/GRCh38#3281565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572616-C-A

3281588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572639-T-C

3281588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572639-T-G

3281607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572656-T-A

http://identifiers.org/hco/20/GRCh38#3281646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572714-C-A

3281646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130572714-C-T

http://identifiers.org/hco/20/GRCh38#3281756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572824-C-A

3281778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572848-A-G

http://identifiers.org/hco/20/GRCh38#3281780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572850-A-C

3281801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572871-G-C

3281801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572871-G-T

3281841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572909-G-A

3281841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572909-G-T

3281842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572910-G-A

3281842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572910-G-T

http://identifiers.org/hco/20/GRCh38#3281869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130572934-C-A

3281869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572934-C-T

3281876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572946-G-C

3281876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572946-G-T

3281891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572957-T-C

3281893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572959-G-A

3281893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572959-G-C

3281893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130572959-G-T

3282393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130573461-C-T

http://identifiers.org/hco/20/GRCh38#3282403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130573463-C-A

3282524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130573583-T-C

3282540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130573599-A-G

3282572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130573630-G-A

3282616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130573670-T-C

3282726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130573774-G-C

3282782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, undefined
orthologous variants: 130573821-C-T

3283055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574195-G-A

3283083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574223-G-A

3283279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574392-T-G

http://identifiers.org/hco/20/GRCh38#3283311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130574425-C-A

3283311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574425-C-T

3283344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574457-T-C

3283444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574537-T-A

3283444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574537-T-G

3283452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574545-G-A

3283452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574545-G-T

3283457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574550-G-A

3283462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130574555-A-T

3286265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130576881-G-A

3286457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130577040-C-T

3286473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130577058-T-C

3286479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130577064-G-C

3286526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130577109-A-G

3286694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130577240-C-T

3286720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130577266-T-C

3287231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578050-T-C

3287253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578063-G-A

3287253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578063-G-C

3287253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578063-G-T

http://identifiers.org/hco/20/GRCh38#3287271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130578083-C-A

3287448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578249-A-G

3287504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578305-C-T

3287565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578325-T-C

3287743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 130578498-G-A

3287743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 130578498-G-C

3287827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578581-C-T

3287878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578632-G-T

http://identifiers.org/hco/20/GRCh38#3287887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130578641-C-A

3287887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578641-C-T

http://identifiers.org/hco/20/GRCh38#3287888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130578642-C-A

3287888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578642-C-T

http://identifiers.org/hco/20/GRCh38#3287929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130578677-C-A

3287929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130578677-C-T

http://identifiers.org/hco/20/GRCh38#3289995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130579157-A-C

3289995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579157-A-G

3290140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 130579310-C-T

3290238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579409-G-A

3290238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579409-G-T

3290288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579440-T-C

3290289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579441-G-T

http://identifiers.org/hco/20/GRCh38#3290305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130579457-C-A

3290305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579457-C-T

3290328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579480-T-C

3290328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130579480-T-G

3290635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130580063-C-T

3291291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130580337-G-A

3291319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130580365-T-C

3294157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130580919-G-A

3294157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130580919-G-T

http://identifiers.org/hco/20/GRCh38#3294177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130580939-C-A

3294280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581040-T-G

3294316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581076-C-T

3294381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581143-T-A

3294381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581143-T-G

3294535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130581298-G-A

3294535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130581298-G-T

3294549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130581312-G-C

3294549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130581312-G-T

3294598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130581358-G-T

3294617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130581377-T-A

3294617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130581377-T-C

3294660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581418-T-G

3294679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581436-T-A

3294679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581436-T-C

3294679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581436-T-G

3294707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130581464-T-C

3296731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130582191-G-A

3296731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130582191-G-T

3296875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130582335-C-T

3296893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130582353-C-G

3296893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130582353-C-T

http://identifiers.org/hco/20/GRCh38#3297038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130582496-C-A

3297065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130582522-T-A

3297065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130582522-T-C

http://identifiers.org/hco/20/GRCh38#3297066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130582523-A-C

3297066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130582523-A-G

3297080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130582537-T-C

3297197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130582653-G-C

3297464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130582901-G-A

3297580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130583039-A-T

3298155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 130583863-A-T

3298163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130583871-T-C

3298163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130583871-T-G

3298468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130584152-C-T

3298586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130584273-T-C

3303706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590007-C-T

3303720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590010-T-C

3303737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590027-C-G

3303737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590027-C-T

3304457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130590622-T-C

3304457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130590622-T-G

http://identifiers.org/hco/20/GRCh38#3304537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130590702-A-C

3304537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 130590702-A-G

3304588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590752-G-T

3304598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130590762-T-C

3311768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130601133-G-A

http://identifiers.org/hco/20/GRCh38#3312461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130601387-C-A

3312461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130601387-C-T

3312668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130601582-C-T

3312807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

3312951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130602464-C-T

3313180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130602689-T-C

3313366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130602853-C-G

3314399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130605866-G-T

3314555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130605998-C-T

3314587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606034-C-G

3314587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606034-C-T

3314592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606038-G-A

3314893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606260-A-T

http://identifiers.org/hco/20/GRCh38#3314913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130606282-C-A

3314950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606306-A-G

3314974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606330-G-A

3314974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606330-G-T

3315001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130606346-T-C

http://identifiers.org/hco/20/GRCh38#3315602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607071-C-A

3315602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130607071-C-T

3315665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130607136-A-T

3315700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130607163-A-G

3315700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130607163-A-T

http://identifiers.org/hco/20/GRCh38#3315895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607735-C-A

3315895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607735-C-T

http://identifiers.org/hco/20/GRCh38#3315909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607743-C-A

3315909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607743-C-G

3315909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607743-C-T

http://identifiers.org/hco/20/GRCh38#3315910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607744-C-A

3315910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607744-C-T

http://identifiers.org/hco/20/GRCh38#3315966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607799-C-A

3315978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607811-G-A

3315978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607811-G-T

http://identifiers.org/hco/20/GRCh38#3316005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607838-C-A

3316040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607872-G-A

3316040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607872-G-T

3316087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 130607918-G-T

http://identifiers.org/hco/20/GRCh38#3316098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130607922-A-C

http://identifiers.org/hco/20/GRCh38#3316579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130609393-C-A

3316579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130609393-C-T

3316676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130609484-G-T

3316692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130609499-G-A

3316692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130609499-G-T

3316768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130609575-G-A

3317987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612370-G-A

http://identifiers.org/hco/20/GRCh38#3318080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130612458-C-A

3318080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612458-C-T

3318216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612520-G-A

3318216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612520-G-T

3318251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612548-G-A

3318251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612548-G-C

3318251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612548-G-T

3318252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612549-G-A

3318252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612549-G-C

3318252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612549-G-T

http://identifiers.org/hco/20/GRCh38#3318329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130612632-A-C

3318411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130612719-T-C

3320474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130615406-C-T

3320553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130615481-G-A

3320701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130615978-C-T

3320765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130616041-T-C

3322181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130616936-A-G

3322181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130616936-A-T

3322399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617224-T-C

3322399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617224-T-G

http://identifiers.org/hco/20/GRCh38#3322401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130617226-C-A

3322401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617226-C-T

3322505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617322-T-C

3322508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617325-G-A

3322508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617325-G-T

3322554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617515-G-T

3322584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617542-C-T

3322587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617545-C-G

3322784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617799-G-C

3322784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617799-G-T

3322797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617812-G-C

3322797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130617812-G-T

3324291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130618591-C-T

3324412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130618722-T-C

3324570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130618833-C-T

3324840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130619073-T-C

http://identifiers.org/hco/20/GRCh38#3325242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130619435-A-C

3325407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130619610-T-C

3325551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130619747-T-C

3325793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130619984-G-C

3326136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130620276-G-C

3326136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130620276-G-T

3326318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130620458-G-T

3329926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130625941-C-T

3330078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626082-A-G

3330079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626083-T-C

3330169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626177-G-A

3330191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626199-C-T

3330521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626242-G-A

3330521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626242-G-T

http://identifiers.org/hco/20/GRCh38#3330524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130626245-C-A

3330524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626245-C-T

3330525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626246-G-A

3330525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130626246-G-T

3330664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130626362-G-A

3330664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130626362-G-T

3332051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130627175-G-C

http://identifiers.org/hco/20/GRCh38#3332128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130627240-C-A

3332128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130627240-C-T

3332150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130627262-G-A

3332367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 130627466-T-C

3332391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130627491-A-G

http://identifiers.org/hco/20/GRCh38#3332396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130627496-C-A

3340171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130632094-A-G

http://identifiers.org/hco/20/GRCh38#3340400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130633683-C-A

3340400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633683-C-T

3340473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633741-T-A

3340473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633741-T-C

3340473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633741-T-G

http://identifiers.org/hco/20/GRCh38#3340475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130633743-A-C

3340475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633743-A-G

http://identifiers.org/hco/20/GRCh38#3340477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130633745-C-A

3340477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633745-C-T

3340486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633754-G-T

3340582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130633850-A-G

3340702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633948-G-A

3340702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633948-G-T

3340713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633953-G-T

http://identifiers.org/hco/20/GRCh38#3340718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130633958-C-A

3340740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633971-G-A

3340740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633971-G-T

3340742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633973-G-A

3340742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633973-G-T

3340747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130633978-G-T

3340791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634021-G-A

3340791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634021-G-C

3340791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634021-G-T

3340801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634031-G-A

3340801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634031-G-T

3340819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634057-T-C

3341059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634458-A-G

3341131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130634517-C-T

3343436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635764-C-T

http://identifiers.org/hco/20/GRCh38#3343540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130635791-C-A

http://identifiers.org/hco/20/GRCh38#3343541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130635792-C-A

3343541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635792-C-T

3343543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635794-T-G

http://identifiers.org/hco/20/GRCh38#3343564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130635812-A-C

3343564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635812-A-G

http://identifiers.org/hco/20/GRCh38#3343616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130635854-C-A

3343616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635854-C-T

3343621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635858-C-T

3343639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130635876-T-C

3343701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130635934-T-A

3343780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636009-C-G

3343802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636027-T-C

3343802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636027-T-G

http://identifiers.org/hco/20/GRCh38#3343831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130636050-A-C

3343831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636050-A-G

3343831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636050-A-T

3343832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636051-G-C

3343832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636051-G-T

3343915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636082-T-A

3343915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636082-T-G

3344126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636287-A-G

3344301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636480-T-C

3344451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636632-G-T

3344492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130636669-T-C

3348145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130639539-G-A

http://identifiers.org/hco/20/GRCh38#3348384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130639814-A-C

3348505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640067-T-A

3348505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640067-T-C

http://identifiers.org/hco/20/GRCh38#3348510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130640072-C-A

3348510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640072-C-G

3348510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640072-C-T

http://identifiers.org/hco/20/GRCh38#3348511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130640073-C-A

3348511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640073-C-G

3348511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640073-C-T

http://identifiers.org/hco/20/GRCh38#3348648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130640206-C-A

3348648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640206-C-T

3348660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640215-T-C

3348895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640329-T-C

3348922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130640363-T-C

3356921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130642795-T-C

3356921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130642795-T-G

3356946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130642820-A-G

3356982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130642856-G-A

3357022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130642898-G-T

3358984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648346-G-T

3359141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648474-A-G

3359185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648514-A-G

http://identifiers.org/hco/20/GRCh38#3359434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130648709-A-C

3359434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648709-A-G

3359436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648711-T-G

3359542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130648817-T-A

3359542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: missense variant
orthologous variants: 130648817-T-C

3359605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648880-G-A

3359605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130648880-G-T

http://identifiers.org/hco/20/GRCh38#3359843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130649212-C-A

3359871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130649245-G-A

http://identifiers.org/hco/20/GRCh38#3359939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130649338-C-A

3359939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130649338-C-G

http://identifiers.org/hco/20/GRCh38#3359976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130649375-C-A

3371534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130650587-G-A

3371792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130650820-T-C

3371967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130650999-A-G

3372141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130651310-G-C

3372310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130651453-C-T

3373140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652239-C-G

3373140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652239-C-T

3373317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652365-C-T

3373361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652398-T-A

3373385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652422-G-A

3374105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130652799-T-C

3374105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130652799-T-G

http://identifiers.org/hco/20/GRCh38#3374215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130652901-C-A

http://identifiers.org/hco/20/GRCh38#3374220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130652906-C-A

3374220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652906-C-G

3374220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652906-C-T

3374292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652951-G-A

3374292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130652951-G-T

3374394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130653055-C-T

3374606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130653223-T-G

3374742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654242-T-A

http://identifiers.org/hco/20/GRCh38#3374897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130654397-C-A

3374897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654397-C-T

3374911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654415-T-A

3374911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654415-T-C

3374911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654415-T-G

3374922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654426-G-T

http://identifiers.org/hco/20/GRCh38#3374924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130654428-C-A

3374924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654428-C-G

3374924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130654428-C-T

http://identifiers.org/hco/20/GRCh38#3375195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130655010-C-A

3375195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655010-C-G

3375195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655010-C-T

3375254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655163-G-A

3375254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655163-G-T

http://identifiers.org/hco/20/GRCh38#3375269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130655178-C-A

3375779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655652-T-C

3375845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655694-C-T

3375846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655695-C-T

3376037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655970-A-T

3376053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655981-A-T

3376056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655984-G-A

3376056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130655984-G-T

3376077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130656005-A-G

3376115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130656057-A-G

3376115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130656057-A-T

3376187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130656108-G-A

3376187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: synonymous variant
orthologous variants: 130656108-G-T

http://identifiers.org/hco/20/GRCh38#3376367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130656283-C-A

3376367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130656283-C-T

http://identifiers.org/hco/20/GRCh38#3376392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130656426-C-A

3378379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130657305-G-C

3378394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130657319-G-T

3378622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130657535-G-A

3380129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130658969-G-A

3380226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130659046-C-T

3380320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130660303-C-T

3380518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130660816-T-C

3381137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130661406-A-G

3381337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662351-T-C

3381516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662526-C-T

3381569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662568-T-A

3381569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662568-T-C

http://identifiers.org/hco/20/GRCh38#3381641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130662620-C-A

3381641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662620-C-T

http://identifiers.org/hco/20/GRCh38#3381642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130662621-C-A

3381642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662621-C-T

3381645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662624-T-C

3381659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662639-C-T

3381696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662675-C-G

3381696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130662675-C-T

3381839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130663066-C-T

3381941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130663154-T-A

3382307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664244-G-C

3382307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664244-G-T

http://identifiers.org/hco/20/GRCh38#3382320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130664257-A-C

3382320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664257-A-G

http://identifiers.org/hco/20/GRCh38#3382332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130664269-C-A

3382332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664269-C-T

3382338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664275-T-C

3382342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664279-A-G

3382342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664279-A-T

http://identifiers.org/hco/20/GRCh38#3382346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130664282-C-A

3382346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664282-C-T

3382352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664288-T-C

3382361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664297-C-T

3382428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 130664342-T-C

3382547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664449-A-G

3382557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664459-G-T

3382639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664519-G-T

3382711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664573-G-C

3382786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664661-C-T

3383074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130664918-C-T

3390676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130669246-A-G

3390714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130669267-G-A

http://identifiers.org/hco/20/GRCh38#3390750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130669304-A-C

3391592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130670060-T-C

3391617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130670084-G-T

3391620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130670087-G-T

3391645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130670096-A-G

3391705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130670160-T-C

3398635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130673337-T-C

3398671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130673373-G-C

3399051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130673705-C-T

3399968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130674577-T-G

3400009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130674609-T-C

3400057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130674656-G-C

3400225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130674807-A-G

3400398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130674955-T-C

3400711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130675716-T-C

3404853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130676146-T-C

3405048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130677188-C-T

3405049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130677189-A-T

3405341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130677477-G-A

3406086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130680074-A-G

3406330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron variant
orthologous variants: 130680961-G-A

http://identifiers.org/hco/20/GRCh38#3406525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130681141-C-A

3407256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681708-C-T

3407422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681840-G-A

3407422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681840-G-C

3407422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681840-G-T

3407454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681863-G-A

3407454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681863-G-C

3407454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130681863-G-T

3407494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 130681903-G-A

3407494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 130681903-G-C

3407494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 130681903-G-T

http://identifiers.org/hco/20/GRCh38#3407520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#130681929-C-A

3407520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 130681929-C-T

3407544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 130681953-G-A

3407544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 130681953-G-T

3407579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130681981-G-A

3407579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130681981-G-C

3407579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17721
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 130681981-G-T