21704938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5 prime UTR variant
orthologous variants: 10706874-C-T

21704988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10706928-G-A

21704988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10706928-G-T

21704991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10706931-G-T

21705050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10706955-A-G

21705075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10706975-G-A

21705075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10706975-G-T

21705162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10707043-G-A

21705162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10707043-G-T

21705276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10707152-A-G

21714350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10710165-T-G

21723917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10711256-G-T

21723932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10711271-G-A

21724252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10711585-G-T

21724262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10711595-A-G

http://identifiers.org/hco/18/GRCh38#21724304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10711637-A-C

http://identifiers.org/hco/18/GRCh38#21725195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10711868-C-A

21725287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10712292-A-G

21725807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10712742-G-T

21727836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10714109-G-A

21728086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10714338-G-A

21728135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10714382-G-A

21728622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10714546-G-C

21740591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10725389-A-G

21740686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10725475-G-C

21740686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10725475-G-T

21740801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10725563-T-C

http://identifiers.org/hco/18/GRCh38#21741221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#10725966-C-A

21741221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10725966-C-T

http://identifiers.org/hco/18/GRCh38#21741920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10726623-A-C

21741920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10726623-A-G

21741946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10726642-G-A

21741946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10726642-G-T

21742321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10726953-G-C

21742321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10726953-G-T

21742651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10727408-C-T

21743050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10727737-G-A

21743320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10728238-T-C

21743438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10728336-T-C

21743485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10728375-G-A

21743985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10728924-T-C

21744235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10729229-T-C

21746434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730339-A-G

21746726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730616-G-A

21746726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730616-G-C

21746808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730685-G-A

21746853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730729-C-T

http://identifiers.org/hco/18/GRCh38#21746990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10730848-C-A

21746990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730848-C-T

21747116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10730966-A-G

21747183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10731035-C-T

21749345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10732913-A-G

21749423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10732980-T-G

21758072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10734270-T-C

21758447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735009-G-A

21758447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735009-G-T

21758461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735015-G-T

21759435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735135-G-A

http://identifiers.org/hco/18/GRCh38#21759602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10735288-C-A

21759602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735288-C-T

21759603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735289-G-A

21759785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735459-A-G

21759992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735655-A-G

21760317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10735943-T-G

21760590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10736194-A-G

21760777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10736399-G-A

21760802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10736424-T-A

21760804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10736426-T-A

21760895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10736486-T-C

21760975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10736561-T-C

21764229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10737862-C-T

21764328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10737928-C-T

21765453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10739980-A-T

21765751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10740964-C-G

21765751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10740964-C-T

21765947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10741157-G-A

21765947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10741157-G-T

http://identifiers.org/hco/18/GRCh38#21766042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10741234-C-A

21766042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10741234-C-T

21766478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10742335-G-C

21766566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10742415-G-A

21766591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10742440-C-T

21766936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10742620-A-G

21766967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10742648-G-A

21768127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10743018-G-T

21768293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10743132-C-T

21768569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10743216-A-G

21768784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10743428-C-G

21772070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10745856-A-G

21772726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10746497-G-A

21772787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10746547-G-A

21772798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10746558-C-T

21773514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10747235-A-T

21773556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10747274-A-G

http://identifiers.org/hco/18/GRCh38#21773569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10747287-C-A

21773569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10747287-C-G

21773569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10747287-C-T

http://identifiers.org/hco/18/GRCh38#21773650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10747382-A-C

21773650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10747382-A-G

http://identifiers.org/hco/18/GRCh38#21773832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10747579-C-A

21773832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10747579-C-T

21774080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10747809-C-G

21775727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10748266-G-A

21775727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10748266-G-T

21775734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10748273-A-G

21775907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10748424-A-G

21777960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749195-A-G

21778011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749239-G-T

http://identifiers.org/hco/18/GRCh38#21778043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10749263-C-A

21778043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749263-C-G

21778091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749311-T-C

21778091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749311-T-G

http://identifiers.org/hco/18/GRCh38#21778441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10749650-A-C

21778472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749683-A-G

21778535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749746-A-G

21778598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749807-T-A

21778766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749959-G-A

21778766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10749959-G-T

http://identifiers.org/hco/18/GRCh38#21778873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10750037-C-A

21779103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10750217-G-T

21779441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10751787-G-A

21779629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10751971-T-A

21779730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10752069-T-C

21779802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10752141-G-A

21779823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10752163-A-G

21780075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10752755-T-G

21788035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10753027-C-T

21791229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10755347-G-A

21791229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10755347-G-T

21791253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10755372-A-G

21791282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10755401-A-G

21791282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10755401-A-T

http://identifiers.org/hco/18/GRCh38#21791358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10755488-A-C

21791358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10755488-A-G

http://identifiers.org/hco/18/GRCh38#21791655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10755797-C-A

21797966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10760711-T-G

21797983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10760728-A-G

21797983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10760728-A-T

21798245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10760962-G-A

http://identifiers.org/hco/18/GRCh38#21798249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10760966-C-A

21798305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10761150-A-G

21798439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10761486-T-C

21798439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10761486-T-G

21798795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10762156-A-G

21798963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10762435-G-A

21798963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10762435-G-T

http://identifiers.org/hco/18/GRCh38#21799104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10762562-A-C

21799216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10762663-T-C

http://identifiers.org/hco/18/GRCh38#21799830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10763178-A-C

21799830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10763178-A-G

21799830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10763178-A-T

21803814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10768040-A-G

http://identifiers.org/hco/18/GRCh38#21803879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10768104-C-A

21803879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10768104-C-T

21804035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10768257-T-C

http://identifiers.org/hco/18/GRCh38#21804071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10768286-C-A

21804175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10768404-G-A

21804186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10768421-A-G

21804272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10768478-A-G

21804330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10768524-A-G

21804942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10769039-T-C

21804993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10769092-A-G

http://identifiers.org/hco/18/GRCh38#21806538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10769840-C-A

21808705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10770884-A-G

http://identifiers.org/hco/18/GRCh38#21813114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10772890-C-A

http://identifiers.org/hco/18/GRCh38#21813224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10773583-C-A

21814501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10775225-T-C

21815534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10775455-G-A

21815795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10775708-C-T

21815876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10775787-A-G

21815884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10775795-T-C

21815920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10775809-T-C

21816865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776528-G-A

21816865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776528-G-T

21816951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776601-A-G

21817060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776706-C-T

21817094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776741-G-A

21817094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776741-G-T

21817129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10776761-T-C

http://identifiers.org/hco/18/GRCh38#21819468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10778111-C-A

21819468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10778111-C-T

21819649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778305-A-G

http://identifiers.org/hco/18/GRCh38#21819674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10778330-C-A

21819674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778330-C-G

21819674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778330-C-T

21819910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778465-T-G

21820257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778799-A-G

21820336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778935-G-A

21820377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10778973-T-G

http://identifiers.org/hco/18/GRCh38#21820560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10779206-A-C

21820722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10779353-G-A

21821900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10779832-C-T

21822430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10780096-T-A

21823273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10781276-G-T

21823318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10781317-T-C

http://identifiers.org/hco/18/GRCh38#21823400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10781397-C-A

http://identifiers.org/hco/18/GRCh38#21823406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10781403-A-C

21824840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10781848-A-G

21824853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10781861-A-G

21825292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10782251-A-G

21825323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10782516-C-T

21825789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10782988-G-A

21825951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10783099-G-T

21826010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10783128-T-C

21826010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10783128-T-G

21826349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10783554-A-G

http://identifiers.org/hco/18/GRCh38#21826402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10783629-C-A

http://identifiers.org/hco/18/GRCh38#21827062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10784330-C-A

21828481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785017-C-T

http://identifiers.org/hco/18/GRCh38#21828581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10785121-C-A

21828715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785261-T-C

http://identifiers.org/hco/18/GRCh38#21828990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10785461-C-A

21828990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785461-C-G

21828990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785461-C-T

21829048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785518-G-A

21829048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785518-G-T

21829348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10785790-A-G

21829963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10786281-T-C

21829969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10786287-G-A

21830339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10786607-A-T

21830342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10786610-C-G

21830350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10786629-T-G

http://identifiers.org/hco/18/GRCh38#21830695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10786950-A-C

21830756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787009-G-T

http://identifiers.org/hco/18/GRCh38#21830829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10787083-C-A

21830993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787262-G-A

http://identifiers.org/hco/18/GRCh38#21831056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10787327-C-A

http://identifiers.org/hco/18/GRCh38#21831105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10787384-C-A

21831109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787388-A-G

21831165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787452-T-C

21831209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787495-T-C

21831243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787529-T-C

21831309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787591-G-T

http://identifiers.org/hco/18/GRCh38#21831380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10787663-C-A

21831380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787663-C-T

21831388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787671-A-G

21831390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10787673-T-C

21831691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10787961-G-A

21832213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10788520-A-T

21832295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10788601-C-G

21832361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10788654-T-C

21832421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10788713-T-C

21832620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10788934-A-G

21833544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10789522-G-A

21833606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10789584-G-A

21833992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10789982-T-C

21834011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10790006-C-T

http://identifiers.org/hco/18/GRCh38#21834259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10790257-C-A

21836742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10791341-A-G

21836851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10791468-A-G

21837643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792300-T-C

21837643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792300-T-G

21837903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792514-T-C

21837903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792514-T-G

21838002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792602-A-G

http://identifiers.org/hco/18/GRCh38#21838246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10792755-C-A

21838246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792755-C-T

21838309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10792822-T-C

21838580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10793088-T-A

21838615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10793132-T-A

21838622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10793139-G-T

21842130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10793502-G-A

21842387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10793743-T-G

21842551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10793959-G-T

21842564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10793979-G-A

21842564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10793979-G-C

21842600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794011-T-C

21842646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794051-T-G

http://identifiers.org/hco/18/GRCh38#21842722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10794113-A-C

21842855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794227-C-G

21842855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794227-C-T

http://identifiers.org/hco/18/GRCh38#21842988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10794339-C-A

21842988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794339-C-T

21843004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794355-T-C

21843004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794355-T-G

21843027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794376-G-A

21843027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794376-G-C

21843027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794376-G-T

http://identifiers.org/hco/18/GRCh38#21843046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10794395-A-C

21843046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10794395-A-T

21844226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10795824-T-A

21844238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10795836-G-T

21844255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 10795853-T-G

21844264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10795862-A-G

http://identifiers.org/hco/18/GRCh38#21844277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10795874-C-A

21844287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10795884-G-A

21846227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10797751-G-A

21846227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10797751-G-C

21846335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10797863-G-A

21846507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798033-G-C

21846645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798129-A-G

21846813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798233-G-A

21846813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798233-G-T

21846829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798251-G-T

http://identifiers.org/hco/18/GRCh38#21846866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10798295-C-A

21846866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798295-C-T

21846872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798301-T-C

21846898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798303-T-C

http://identifiers.org/hco/18/GRCh38#21847027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10798435-C-A

21847027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10798435-C-T

21847172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798577-T-G

http://identifiers.org/hco/18/GRCh38#21847185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10798590-C-A

21847185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798590-C-T

21847673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10798913-A-G

21847791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10799050-T-C

21848894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10799547-T-C

21849171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10800031-G-A

21849171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10800031-G-T

21849280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10800140-G-A

21849280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10800140-G-C

http://identifiers.org/hco/18/GRCh38#21849402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10800274-A-C

21849402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10800274-A-G

21849458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10800312-T-G

21849648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10800495-A-T

21849666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10800508-G-C

21851767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10800957-A-G

21852307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10801444-G-A

21852311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10801456-G-T

21852455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10801651-A-G

21852564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10801742-G-T

21852565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10801743-C-G

http://identifiers.org/hco/18/GRCh38#21852639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10801829-C-A

21852927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10802097-T-C

21853098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10802224-T-A

21853175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10802296-A-G

21853236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10802358-A-G

21853254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10802376-T-C

http://identifiers.org/hco/18/GRCh38#21853338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10802456-C-A

21853338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10802456-C-G

21853710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10802896-G-A

21853776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10803192-C-T

21853798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10803207-A-G

21856844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10804350-A-G

21857088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10804647-A-G

21857105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10804669-A-G

21857199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10804756-T-C

http://identifiers.org/hco/18/GRCh38#21857330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10804875-C-A

http://identifiers.org/hco/18/GRCh38#21857364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10804909-C-A

21857364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10804909-C-T

http://identifiers.org/hco/18/GRCh38#21858676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10808161-C-A

21858676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10808161-C-T

21858710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10808195-A-G

21858712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10808197-T-C

21858744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10808235-G-A

http://identifiers.org/hco/18/GRCh38#21858785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10808272-A-C

21860666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10808661-A-G

http://identifiers.org/hco/18/GRCh38#21861094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10808991-C-A

21861158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10809056-A-G

http://identifiers.org/hco/18/GRCh38#21861175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10809073-A-C

21861175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10809073-A-G

21861175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10809073-A-T

21861190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10809088-A-G

21862642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10811076-T-A

21862702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10811131-G-T

21862931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10811307-T-A

21862931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10811307-T-C

21862958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10811334-A-G

21864474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10811928-A-G

21864582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10812041-C-G

21864582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 10812041-C-T

21864722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812181-G-C

21864722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812181-G-T

21864785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812267-G-T

21864855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812379-T-C

21864855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812379-T-G

21864922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812446-G-A

21864922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812446-G-T

21864972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812486-T-C

21865117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812625-T-A

21865119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812629-A-G

21865155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812667-A-G

21865155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10812667-A-T

21865562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10813058-G-T

21865874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10813321-T-C

21865898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10813348-T-C

21866033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10813481-A-G

21866454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814058-T-C

21866627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814213-T-C

21866627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814213-T-G

21866629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814215-G-A

21866629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814215-G-C

21866795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814387-G-T

21867313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814846-G-T

21867383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10814917-T-C

http://identifiers.org/hco/18/GRCh38#21867399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10814929-C-A

http://identifiers.org/hco/18/GRCh38#21867406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10814936-C-A

21867569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10815096-T-C

21867793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10815313-C-T

21867915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10815437-G-A

http://identifiers.org/hco/18/GRCh38#21868183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#10815793-C-A

21868201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10815811-C-T

21868224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10815832-G-T

21868414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10815994-C-T

21868728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10816302-A-G

21868994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10816569-C-T

21869171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10816752-C-T

21869218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10816800-A-G

21869547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10817116-G-T

21870198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10817777-A-G

21870440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10818019-T-C

21870539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10818145-C-T

21870612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10818252-G-T

21870870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10818493-G-T

21870896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21086
most severe consequence: 3 prime UTR variant
orthologous variants: 10818519-G-C