24848701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21048486-C-T

24849028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21048813-G-T

24849235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049030-G-A

24849359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049153-T-G

24849424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049211-A-G

http://identifiers.org/hco/10/GRCh38#24849595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21049378-C-A

24849595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049378-C-T

24849629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049405-G-T

24849658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049434-T-C

http://identifiers.org/hco/10/GRCh38#24849661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21049437-C-A

24849661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049437-C-T

24849757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049531-C-T

24849761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049534-G-A

24849761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049534-G-T

24849763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049536-G-A

24849794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049567-A-G

24849820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3 prime UTR variant
orthologous variants: 21049599-C-T

24849874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: synonymous_variant, undefined
orthologous variants: 21049649-A-G

24849959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21049835-A-G

http://identifiers.org/hco/10/GRCh38#24850009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21049885-A-C

24850947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21050891-C-T

24851156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051083-T-C

http://identifiers.org/hco/10/GRCh38#24851316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21051174-C-A

24851316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051174-C-G

24851316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051174-C-T

24851342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051211-A-T

24851369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051235-A-T

24851399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21051265-T-G

24851415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21051281-A-G

24851425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, missense_variant
orthologous variants: 21051291-T-C

http://identifiers.org/hco/10/GRCh38#24851435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21051301-C-A

24851435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, missense_variant
orthologous variants: 21051301-C-G

24851445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21051311-T-C

24851573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051417-G-T

24851709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051533-G-C

24851925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051743-T-C

24851970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051788-A-G

24851997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21051815-T-C

24852747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21052096-T-C

24852757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21052106-A-G

24855091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21052809-T-C

http://identifiers.org/hco/10/GRCh38#24855264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21052913-C-A

24855264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21052913-C-T

24855371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21053022-T-A

24855371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 21053022-T-C

http://identifiers.org/hco/10/GRCh38#24856624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21053193-A-C

24856630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053199-C-T

24856673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053241-G-A

24856803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053355-T-A

24856862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053394-T-G

24856930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: missense variant
orthologous variants: 21053459-G-T

24857044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053570-A-G

24857134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053661-G-A

24857134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053661-G-T

24857142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053669-T-C

24857144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053671-T-C

24857261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053778-T-C

24857264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053781-A-G

24857369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053895-A-G

24857408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21053934-C-T

24857514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21054034-G-A

24857572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21054094-G-A

24857671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21054193-G-T

http://identifiers.org/hco/10/GRCh38#24857695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21054216-C-A

24857884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21054338-A-G

24857937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21054378-T-C

24858188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21054610-G-A

24858371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21054788-G-A

24858406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: missense_variant, undefined
orthologous variants: 21054824-C-T

24858481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21054925-G-T

http://identifiers.org/hco/10/GRCh38#24858517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#21054961-C-A

24858663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055314-G-A

24858928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055539-G-A

24858976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055588-A-G

24858976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055588-A-T

24858988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055600-G-A

24858988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055600-G-C

24859845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055750-A-G

http://identifiers.org/hco/10/GRCh38#24859934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21055830-A-C

24859934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055830-A-G

24860013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21055905-C-G

24860454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21056221-T-C

24860506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21056265-T-G

24860899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21056606-T-A

24861014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21056719-T-G

24861067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21056812-A-T

24861096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21056836-T-C

24865684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21058790-T-G

24865951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059032-G-A

24866223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059163-T-C

24867190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059657-T-A

24867327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059753-G-C

24867458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059925-T-C

24867463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059930-T-C

24867480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21059935-T-C

http://identifiers.org/hco/10/GRCh38#24868307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21060185-C-A

24868307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21060185-C-T

24868383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21060279-G-C

24870584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21063805-T-G

24870599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21063820-T-A

24870707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21063922-T-C

24870779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21063979-A-G

24871198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21064129-T-C

24871448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21064389-G-A

24871479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21064420-G-A

24871521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21064546-A-G

http://identifiers.org/hco/10/GRCh38#24871895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21064895-A-C

24872147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21065160-T-C

24872365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21065359-T-C

24872447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21065440-C-T

24872616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21065582-A-T

24873205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21065697-G-T

24873486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21065990-T-C

http://identifiers.org/hco/10/GRCh38#24873572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21066076-C-A

24873596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066098-C-T

24873700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066197-G-C

24873707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066204-T-C

24873807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066262-A-G

24873841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066274-G-A

http://identifiers.org/hco/10/GRCh38#24873862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21066295-C-A

http://identifiers.org/hco/10/GRCh38#24873906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21066307-A-C

24873906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066307-A-T

24873926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066321-G-A

24873926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066321-G-T

24873928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066323-G-A

24873928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066323-G-T

24874422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21066913-G-C

http://identifiers.org/hco/10/GRCh38#24874509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21066986-C-A

24875646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067310-T-C

http://identifiers.org/hco/10/GRCh38#24875731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21067407-C-A

24875775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067440-C-G

24875795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067460-A-G

24875877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067611-A-G

24875877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067611-A-T

http://identifiers.org/hco/10/GRCh38#24875890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21067624-C-A

24875890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067624-C-T

24875892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067626-G-A

24875892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067626-G-T

24875903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067642-T-C

24875927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067659-C-T

24875928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067660-T-C

24876012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21067734-C-T

http://identifiers.org/hco/10/GRCh38#24876030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21067752-C-A

24878317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21070613-C-T

24878329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21070625-G-A

24878548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21070796-T-A

24879039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21071191-A-T

24879065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21071217-A-T

24879116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21071264-C-T

24879364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21071524-A-T

24879590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21071693-T-C

24879596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21071699-C-T

24879973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21072026-T-A

24879973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21072026-T-C

24879996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21072049-C-T

24880008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21072067-G-A

24880024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21072083-C-T

24880115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21072174-T-C

http://identifiers.org/hco/10/GRCh38#24883440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21074675-C-A

http://identifiers.org/hco/10/GRCh38#24883478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21074712-A-C

http://identifiers.org/hco/10/GRCh38#24883721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21074918-A-C

24883721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21074918-A-G

24888828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21076722-A-G

24888862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21076756-G-A

24889012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21076871-G-A

24889028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21076877-C-T

24889037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21076886-G-A

24889037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21076886-G-C

24889419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21077338-T-C

24889705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21077632-T-C

24890050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21077984-G-A

24890097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21078039-A-G

24890353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21078278-A-G

24890517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21078417-C-T

24890537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21078432-A-G

24890614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21078494-C-T

24890634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21078515-A-G

24890942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21086851-C-T

24891037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21086930-G-A

24891047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21086940-A-G

24891076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21086968-G-A

24893130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21088473-C-T

24893149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21088493-A-G

24893901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21088991-T-C

24893916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089006-T-A

24894392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21089145-G-A

http://identifiers.org/hco/10/GRCh38#24894510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#21089267-C-A

24894785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089510-C-T

24894910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089647-G-A

24894910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089647-G-C

24894913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089650-T-C

24895690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089679-T-G

24895731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089719-G-A

24895731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089719-G-C

24895731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089719-G-T

24895880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21089839-C-G

24897376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21090379-C-G

24897376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21090379-C-T

http://identifiers.org/hco/10/GRCh38#24897560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#21090567-A-C

24897563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21090570-G-A

24897587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21090594-T-A

24897606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21090613-G-A

24897608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21090615-A-G

24897719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21090734-T-C

24897797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21090804-T-C

24898112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21091059-A-G

24898124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21091073-G-A

24899180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21092699-A-G

24899330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21092835-T-A

24899491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21092972-G-A

24899530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21093011-G-T

24899616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21093088-C-T

24899660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21093129-C-T

24899769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21093215-G-A

24899813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21093259-G-A

24899869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21093314-C-T

24900795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21094548-C-T

24901169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21095562-C-T

24901298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21095743-G-A

24901365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21095834-A-G

24901993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21096397-G-A

24902000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21096404-G-T

24902012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21096416-T-C

24902078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21096482-C-T

24902311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21096701-C-T

24902396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21096787-T-A

24902396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21096787-T-C

http://identifiers.org/hco/10/GRCh38#24902405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#21096796-A-C

24902776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21097145-C-G

http://identifiers.org/hco/10/GRCh38#24904060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21098092-C-A

24904131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098156-A-G

24904143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098168-C-G

24904148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098173-G-C

24904387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098447-G-A

24904456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098518-T-A

24904577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098637-C-T

24904761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21098988-C-T

http://identifiers.org/hco/10/GRCh38#24904823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21099041-C-A

24905661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21099243-G-A

24905664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21099246-T-C

24905817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21099395-T-A

24906141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21101712-C-T

24906279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21101850-A-G

24906574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102112-G-A

24906592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102129-G-C

24906681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102227-C-T

24906685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102231-T-C

24906761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102299-T-C

http://identifiers.org/hco/10/GRCh38#24906771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21102309-C-A

24906824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102353-T-A

24907685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102700-G-A

24907747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102760-T-C

24907824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21102825-C-G

24908175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21103173-G-A

24908175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21103173-G-T

http://identifiers.org/hco/10/GRCh38#24908188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21103186-C-A

24908188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21103186-C-G

24908188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21103186-C-T

http://identifiers.org/hco/10/GRCh38#24908267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21103266-C-A

24908268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21103267-T-G

http://identifiers.org/hco/10/GRCh38#24908490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21103454-C-A

24908490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 21103454-C-T

24908503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21103467-C-T

24908507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, missense_variant
orthologous variants: 21103475-T-C

24909678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21104578-A-G

24909818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21104717-A-G

24910409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21105101-A-G

24910991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21105665-G-A

24910995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21105669-T-C

24911010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21105687-T-A

24911033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21105710-G-A

24911269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21105953-A-G

24911354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21106036-G-A

24911354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21106036-G-T

24911558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21106233-C-G

24912443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21106449-G-A

24912954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21106940-G-A

24913140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21107121-T-C

24913356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21107312-T-C

http://identifiers.org/hco/10/GRCh38#24913423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21107379-A-C

24913720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21107638-G-A

24914108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21107982-A-G

24914203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21108070-T-G

http://identifiers.org/hco/10/GRCh38#24914340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21108206-A-C

24914379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21108245-T-C

24914438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21108304-G-A

24914529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21108392-C-T

24915245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21110346-T-C

24915311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21110421-G-A

24915368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21110471-G-A

24915403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21110506-T-G

24915422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21110525-G-T

24915522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21110720-A-G

24915676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111104-T-C

24915676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111104-T-G

24915731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111214-G-T

24915769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111256-C-G

24915959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111402-G-A

24916007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111447-T-G

http://identifiers.org/hco/10/GRCh38#24916249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21111637-C-A

24916249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111637-C-T

24916403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21111729-C-T

24916841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112139-G-A

24916961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112243-G-A

24917206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112486-G-A

24917375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112653-G-A

24917382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112660-T-A

24917432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112704-A-G

24917466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112734-T-C

24917515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21112774-A-G

24917917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21113731-A-T

24917930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21113744-C-G

http://identifiers.org/hco/10/GRCh38#24918407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21114161-C-A

24920883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21114990-T-C

24920916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21115019-C-G

http://identifiers.org/hco/10/GRCh38#24920938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21115040-C-A

24920938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21115040-C-T

24921092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21115646-T-C

24921517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21116491-G-C

http://identifiers.org/hco/10/GRCh38#24921626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#21116621-C-A

24921626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21116621-C-T

24921652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21116647-G-T

24921718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21116706-A-G

http://identifiers.org/hco/10/GRCh38#24935210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21122770-A-C

24935242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21122811-G-A

24935347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21122909-G-A

24935429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21123259-C-T

24935801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21123987-G-T

24935917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124107-C-T

24936126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124287-G-A

24937093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124541-T-A

http://identifiers.org/hco/10/GRCh38#24937291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21124731-C-A

24937389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124834-T-C

24937464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124884-T-C

24937477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124897-G-A

24937477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124897-G-C

24937477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124897-G-T

http://identifiers.org/hco/10/GRCh38#24937485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21124905-C-A

24937485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21124905-C-T

http://identifiers.org/hco/10/GRCh38#24937494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21124914-C-A

24937861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21125878-T-C

24942088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129671-T-C

24942098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129680-T-A

24942098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129680-T-C

24942181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129753-T-G

http://identifiers.org/hco/10/GRCh38#24942217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21129787-C-A

24942217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129787-C-G

24942217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129787-C-T

24942246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129802-G-A

24942246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129802-G-T

24942247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129803-G-A

24942247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129803-G-C

24942247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129803-G-T

24942256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129812-G-T

24942257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129813-T-C

24942257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129813-T-G

http://identifiers.org/hco/10/GRCh38#24942258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21129814-A-C

24942258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129814-A-G

24942287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129842-G-A

http://identifiers.org/hco/10/GRCh38#24942302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21129854-C-A

24942314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21129863-A-G

24942334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: missense variant
orthologous variants: 21129887-C-T

24942410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: missense variant
orthologous variants: 21129968-G-C

24942449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21130007-T-C

24942477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21130033-G-A

http://identifiers.org/hco/10/GRCh38#24942497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21130056-C-A

24942573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21130180-A-G

24942573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21130180-A-T

24943253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21130834-G-C

24943974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21131232-T-C

24944879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21133604-C-T

24945188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134149-C-T

24945269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134229-T-C

http://identifiers.org/hco/10/GRCh38#24945339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21134283-A-C

24945395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134336-G-T

24945749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134385-G-C

24945807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134425-C-T

http://identifiers.org/hco/10/GRCh38#24945815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21134433-C-A

24945928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134533-T-C

24946122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134689-T-C

24946165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134727-G-A

24946188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21134751-A-T

24946543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21135880-A-G

24946565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21135902-A-G

24946594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21135931-A-G

24946594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21135931-A-T

http://identifiers.org/hco/10/GRCh38#24946604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21135941-C-A

24946828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136101-T-A

24947104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136171-C-T

24947248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136281-T-C

24947450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136486-G-T

24947575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136596-G-T

24947761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136967-T-C

24947796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21136993-G-T

24947861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21137047-C-T

24947978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21137126-A-G

24948006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21137148-A-G

24948079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21137179-G-T

24948107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21137199-T-C

24948153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21137237-G-A

24948189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: 21137279-T-C

http://identifiers.org/hco/10/GRCh38#24948260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21137333-A-C

http://identifiers.org/hco/10/GRCh38#24948355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#21137422-A-C

24950719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21144430-G-A

24950719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21144430-G-C

24950832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21144555-G-A

24950832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21144555-G-T

24951060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21144748-G-A

24951113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21144804-A-G

24951512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21145844-T-C

24951631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21145981-C-T

24951667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146011-T-C

24952033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146222-G-C

24952033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146222-G-T

24952174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146348-G-A

24952224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146395-C-T

24952355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146526-G-A

24952355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146526-G-T

http://identifiers.org/hco/10/GRCh38#24952380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21146551-C-A

24952411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21146582-A-G

24952412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21146583-G-A

24952412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21146583-G-T

http://identifiers.org/hco/10/GRCh38#24952440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21146609-C-A

24952440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21146609-C-G

24952440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21146609-C-T

24952480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146658-G-A

24952480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146658-G-C

24952480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron variant
orthologous variants: 21146658-G-T

http://identifiers.org/hco/10/GRCh38#24952530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#21146720-C-A

24952530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23333
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 21146720-C-T