http://identifiers.org/hco/16/GRCh38#12661316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11620769-C-A

http://identifiers.org/hco/16/GRCh38#12661414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11620865-C-A

12661509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11620951-T-C

http://identifiers.org/hco/16/GRCh38#12662071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#11621474-C-A

12662154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11621555-G-T

12662236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11621614-G-C

http://identifiers.org/hco/16/GRCh38#12663414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11621958-C-A

12663530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11622060-A-G

http://identifiers.org/hco/16/GRCh38#12664083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11622592-C-A

12664281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11622725-T-G

12664328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11622780-C-G

12664328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11622780-C-T

http://identifiers.org/hco/16/GRCh38#12664568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11622930-A-C

http://identifiers.org/hco/16/GRCh38#12664582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11622942-C-A

http://identifiers.org/hco/16/GRCh38#12664628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11622988-C-A

12664628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11622988-C-G

12664702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11623053-T-C

12664702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11623053-T-G

http://identifiers.org/hco/16/GRCh38#12664704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11623055-C-A

12664780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11623125-T-C

http://identifiers.org/hco/16/GRCh38#12664805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11623149-C-A

12664883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11623216-G-A

12664883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3 prime UTR variant
orthologous variants: 11623216-G-C

12664915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 11623247-C-G

12664915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 11623247-C-T

12664928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 11623260-T-C

12665096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11623428-T-A

12665096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11623428-T-C

12665151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11623484-G-A

12665151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11623484-G-T

12674317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625279-C-G

12674381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625333-G-A

12674381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625333-G-T

http://identifiers.org/hco/16/GRCh38#12674406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11625359-C-A

12674423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625376-T-C

12674586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625505-G-A

12674657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625564-G-A

12674777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625653-C-T

12674797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625673-G-A

12674810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625686-C-T

12675009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625851-G-A

12675068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11625910-T-C

12675181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11626021-T-C

12675265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11626103-G-C

12675284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11626122-T-C

12675462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11626278-G-A

12675809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11626586-T-A

12675812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11626589-G-A

12678036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11627361-T-C

12679635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11631936-T-G

12679669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11631971-C-T

http://identifiers.org/hco/16/GRCh38#12681422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11632482-C-A

12681562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11632598-T-C

12681890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11632905-T-C

12682006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633027-T-C

12682565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633250-G-A

12682571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633256-C-T

12682590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633281-A-G

12682794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633466-C-T

12682844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633516-G-A

12682873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11633545-G-T

12685645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11634905-T-C

12685673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11634925-T-C

12685675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11634927-C-T

12685819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11635053-A-T

http://identifiers.org/hco/16/GRCh38#12686026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11635242-C-A

12686096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11635297-G-A

12686096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11635297-G-T

12694306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11638984-G-C

12694507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639183-G-C

12694520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639196-G-C

http://identifiers.org/hco/16/GRCh38#12694584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11639257-C-A

12694584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639257-C-T

12694718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639386-G-A

http://identifiers.org/hco/16/GRCh38#12694728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11639396-A-C

12695945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639601-G-C

12695976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639632-A-G

12696218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639820-C-T

12696338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639905-G-C

12696421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11639979-T-C

12698742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11642265-T-C

12698745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11642268-T-A

12699090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11642622-G-A

http://identifiers.org/hco/16/GRCh38#12699225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11642756-A-C

12699340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11642870-G-A

12699619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643160-T-C

12699619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643160-T-G

12699761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643302-G-A

http://identifiers.org/hco/16/GRCh38#12699938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11643476-A-C

12699938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643476-A-G

12699985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643530-G-A

http://identifiers.org/hco/16/GRCh38#12699994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11643539-C-A

12700038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643581-G-A

12700137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643664-C-G

12700137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643664-C-T

12700163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643683-G-C

12700177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11643697-C-G

12703934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645440-G-A

12704121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645644-A-G

12704140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645663-G-A

12704215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645741-G-A

12704391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645854-C-G

12704399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645862-C-T

12704500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645962-T-A

12704500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645962-T-C

12704500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11645962-T-G

12704609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11646026-G-A

12704667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, missense_variant
orthologous variants: 11646082-G-C

12704667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, missense_variant
orthologous variants: 11646082-G-T

12704814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11646226-G-A

12704832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11646244-C-T

12704895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11646307-A-G

12704931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11646343-G-A

12704931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11646343-G-C

12704931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11646343-G-T

12711026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651121-T-C

12711063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651167-G-C

12711155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651265-A-T

12711180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651288-G-A

http://identifiers.org/hco/16/GRCh38#12711371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11651476-C-A

12711603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651610-T-C

12711686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651686-T-G

12711697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651697-G-A

12711880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651848-T-C

12711881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651849-G-A

12711881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651849-G-C

12712034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651968-G-T

12712075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11651985-T-C

12712271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11652072-A-G

12713049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11652754-A-G

http://identifiers.org/hco/16/GRCh38#12713163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11652861-C-A

http://identifiers.org/hco/16/GRCh38#12721203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11655197-C-A

12721277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655272-A-G

12721324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655318-A-G

12721356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655350-C-T

12721533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655488-T-A

12721533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655488-T-G

12721569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655520-A-G

12721861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655788-A-T

http://identifiers.org/hco/16/GRCh38#12721867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11655794-C-A

12721889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11655816-T-C

12722130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11656034-C-G

12723232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11656528-T-C

12723391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11656689-G-A

12723391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11656689-G-C

12723734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11656944-C-T

12723806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11657002-G-A

12723806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11657002-G-T

12723880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11657071-G-A

12723896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11657089-C-T

12735813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11660129-T-A

12735951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11660270-C-T

12736088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11660369-T-C

12736124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11660404-A-G

12738174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11663295-G-C

12738177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11663298-C-T

12738366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11663481-T-G

12738729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11663833-A-G

12738994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11664084-C-T

12739068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11664157-G-A

12740721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11664816-G-C

12740721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11664816-G-T

12740969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670661-G-A

12741043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670719-C-T

12741167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670845-G-C

12741269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670938-G-A

12741269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670938-G-T

http://identifiers.org/hco/16/GRCh38#12741270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11670939-C-A

12741270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670939-C-T

12741330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11670987-A-T

12741709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11671347-T-C

12741740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11671379-G-A

12742167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11671945-C-G

12742275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11672028-G-T

12742312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11672065-G-A

12742499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11672251-T-C

12742831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11672572-G-C

12742951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11672642-C-T

12743023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11672701-G-A

12751460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11675872-C-T

12751658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11676067-T-G

12751832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11676233-T-C

12751930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11676325-T-C

12752043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11676446-A-T

http://identifiers.org/hco/16/GRCh38#12752209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11676580-C-A

12752385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11676744-C-T

12757386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11684959-C-T

12757941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11685467-G-A

12757969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11685489-T-C

12758029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11685530-A-G

http://identifiers.org/hco/16/GRCh38#12758185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11685674-C-A

12760386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688741-G-A

12760386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688741-G-T

12760398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688753-G-A

12760447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688795-T-C

12760472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688819-A-T

12760530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688830-G-A

12760530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688830-G-C

12760530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688830-G-T

12760634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688920-T-C

12760639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11688925-A-G

12760969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11689237-G-T

12761004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11689276-A-G

12761043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11689319-G-C

12761043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11689319-G-T

12761516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11689920-G-A

12765264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11690630-C-T

http://identifiers.org/hco/16/GRCh38#12765752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11692772-A-C

12765886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11692901-A-G

12765978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11692991-C-G

http://identifiers.org/hco/16/GRCh38#12766063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11693067-A-C

12766070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11693074-C-T

12766127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11693129-T-C

12766147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11693149-C-G

12766152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11693154-G-A

12766164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11693163-G-A

12768238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11694049-T-C

12768264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11694080-A-G

http://identifiers.org/hco/16/GRCh38#12768450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11694283-C-A

12768450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11694283-C-T

12769423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11696884-C-T

12769427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11696885-G-A

http://identifiers.org/hco/16/GRCh38#12769612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11697070-C-A

12769612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697070-C-G

12769685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697143-G-A

12769829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697270-T-C

12769829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697270-T-G

12770241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697645-T-C

12770250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697651-T-C

12770253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697654-T-C

12770469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697853-G-A

12770510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11697884-G-A

12770606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698005-T-C

12770640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698035-T-C

12770805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698133-G-A

12770882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698211-A-G

12770888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698217-G-A

12770888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698217-G-C

12770890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698219-G-A

12770891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698220-G-A

12770891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698220-G-C

12770978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698244-G-A

12771260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698346-T-A

http://identifiers.org/hco/16/GRCh38#12771485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11698474-C-A

12771485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698474-C-T

http://identifiers.org/hco/16/GRCh38#12771486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11698475-C-A

12771644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698632-T-C

12771706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698694-C-T

12771730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698719-C-T

http://identifiers.org/hco/16/GRCh38#12771803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11698796-C-A

12771837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698830-T-A

12771882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11698855-G-A

http://identifiers.org/hco/16/GRCh38#12771983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11698878-C-A

http://identifiers.org/hco/16/GRCh38#12772420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11699104-A-C

12772578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11699254-G-C

12772759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11699439-A-G

12772788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11699468-C-G

12773250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11699912-C-T

12773400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11700062-T-C

http://identifiers.org/hco/16/GRCh38#12777154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11700941-A-C

12777164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11700951-G-A

12777198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11700983-T-C

http://identifiers.org/hco/16/GRCh38#12777332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11701113-A-C

12777332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11701113-A-G

12777529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11701311-T-C

12777572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11701345-A-G

12777576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11701349-G-A

12777744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11701468-T-C

12778780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11701851-G-C

12779154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11702199-C-T

12779205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11702243-G-A

12780005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron variant
orthologous variants: 11703505-G-A

12781041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11705302-A-G

12781041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11705302-A-T

http://identifiers.org/hco/16/GRCh38#12781064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11705325-C-A

12781064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11705325-C-G

12781064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11705325-C-T

12781098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11705354-T-G

http://identifiers.org/hco/16/GRCh38#12781099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11705355-C-A

12781099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11705355-C-T

12781178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 11705435-G-C

12781275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11705532-G-A

12781308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11705565-T-C

12781315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11705572-G-C

12781342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11705599-C-G

12781394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11705651-C-T

12781437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11705675-A-G

12781482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11705720-T-C

12781482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11705720-T-G

http://identifiers.org/hco/16/GRCh38#12781620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11705858-C-A

12781620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11705858-C-T

12781635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11705873-T-A

12781697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11705935-A-G

12782049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11706292-C-T

12787407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11711526-T-C

12787429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11711546-G-T

12787741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11711847-G-C

12787775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11711881-T-C

12787832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11711938-T-C

http://identifiers.org/hco/16/GRCh38#12788215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11712221-C-A

12788222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712228-A-G

http://identifiers.org/hco/16/GRCh38#12788435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11712547-C-A

12788435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712547-C-T

12788711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712739-A-T

12788796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712825-T-C

12788796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712825-T-G

12788797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712826-G-A

12788863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11712894-C-T

12790302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11714020-A-G

http://identifiers.org/hco/16/GRCh38#12790433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11714143-C-A

12790433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11714143-C-G

12790510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11714216-T-G

12790517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11714223-A-G

12793512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11717275-T-A

http://identifiers.org/hco/16/GRCh38#12793524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#11717287-A-C

http://identifiers.org/hco/16/GRCh38#12793632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11717364-C-A

http://identifiers.org/hco/16/GRCh38#12793924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11717645-C-A

12794004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11717724-T-C

http://identifiers.org/hco/16/GRCh38#12794088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11717789-C-A

12794099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11717800-T-C

12794206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11717886-G-C

12794396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718015-G-A

12794402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718021-G-A

http://identifiers.org/hco/16/GRCh38#12794416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11718035-A-C

http://identifiers.org/hco/16/GRCh38#12794443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11718048-A-C

12794443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718048-A-G

http://identifiers.org/hco/16/GRCh38#12794463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11718064-A-C

12794463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718064-A-T

12794513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718104-G-A

http://identifiers.org/hco/16/GRCh38#12794563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11718120-C-A

http://identifiers.org/hco/16/GRCh38#12794755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11718185-A-C

12794829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718221-A-G

12794920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718309-G-A

12795686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718686-A-G

12795747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718723-G-A

12795784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11718747-A-T

12798196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11722918-A-G

12798219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11722941-C-T

12798242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11722964-G-A

12798242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11722964-G-C

http://identifiers.org/hco/16/GRCh38#12798747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11724115-A-C

http://identifiers.org/hco/16/GRCh38#12798950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11724285-C-A

http://identifiers.org/hco/16/GRCh38#12799041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11724370-A-C

12801509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11725312-G-A

http://identifiers.org/hco/16/GRCh38#12801585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#11725389-C-A

12801658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11725451-T-C

12801709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11725500-A-G

12801800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11725589-G-A

12801807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11725596-T-A

12801864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11725646-C-T

12802061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11725809-C-G

http://identifiers.org/hco/16/GRCh38#12803088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#11726640-A-C

12803316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11726794-G-A

12803316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11726794-G-T

12803579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11726998-G-A

12803579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11726998-G-T

12803627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11727046-G-A

12803627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11727046-G-T

12803644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11727063-G-A

12803644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11727063-G-T

12803674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11727093-G-A

12803674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11727093-G-T

12803830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25632
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11727247-G-A