122202935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972354-T-C

122202981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972402-T-C

122203025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972445-C-T

122203194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972594-G-A

122203194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972594-G-T

122203643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972959-G-T

122203661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35972974-T-C

122203869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973185-G-A

122203869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973185-G-T

122203878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973194-G-A

122203878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973194-G-T

122203915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973231-G-T

122203995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973298-C-G

122204259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973557-C-T

122204327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973625-G-T

122204454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973751-G-A

122204454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973751-G-T

122204473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973774-G-A

http://identifiers.org/hco/9/GRCh38#122204643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35973952-C-A

122204643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973952-C-G

122204643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3 prime UTR variant
orthologous variants: 35973952-C-T

122204861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35974164-G-C

122204861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35974164-G-T

122204899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35974202-A-G

122206094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35974865-C-T

122206161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35974935-G-A

122206253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35975022-C-T

http://identifiers.org/hco/9/GRCh38#122206367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35975109-A-C

122206459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35975208-C-T

122206500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35975248-G-C

122206862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35975573-C-T

122207190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35975859-T-C

122207454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35976102-C-T

122209595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977361-C-T

122209635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35977401-C-T

122209641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35977407-A-G

122209646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, missense_variant
orthologous variants: 35977412-T-C

122209758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977524-G-A

122209758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977524-G-T

122209781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977548-G-A

122209781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977548-G-T

122209812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977570-G-T

http://identifiers.org/hco/9/GRCh38#122209819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35977577-C-A

122209819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977577-C-T

122209831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35977589-C-T

122212152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35979606-G-C

122212156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35979610-A-G

122212662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35980063-C-G

122212662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35980063-C-T

122213477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35980850-G-A

122213477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35980850-G-C

122213477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35980850-G-T

http://identifiers.org/hco/9/GRCh38#122213610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35980978-A-C

http://identifiers.org/hco/9/GRCh38#122213832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35981202-C-A

http://identifiers.org/hco/9/GRCh38#122213887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35981242-C-A

122213887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35981242-C-G

122213887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35981242-C-T

122214124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981459-G-A

122214124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981459-G-T

http://identifiers.org/hco/9/GRCh38#122214183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35981521-C-A

122214183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981521-C-T

http://identifiers.org/hco/9/GRCh38#122214211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35981550-C-A

122214236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981575-C-T

http://identifiers.org/hco/9/GRCh38#122214258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35981592-C-A

122214258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981592-C-G

122214258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981592-C-T

122214259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981593-G-A

122214259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981593-G-C

122214259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981593-G-T

122214440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35981776-G-T

122214659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35981922-C-T

122214765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35982048-A-G

122214769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35982052-G-A

122215045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35982426-T-C

http://identifiers.org/hco/9/GRCh38#122215118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35982512-A-C

122216059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983300-G-A

122216059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983300-G-T

122216253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983509-C-G

122216253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983509-C-T

122216359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983640-G-A

122216485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983781-A-T

122216756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983983-G-C

122216801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35983998-T-G

122216895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35984061-A-T

122216917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35984082-A-G

122216917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35984082-A-T

122216972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35984136-A-G

122216998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35984163-T-C

122217090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35984247-G-A

122217138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35984295-G-A

122217138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35984295-G-C

122217138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35984295-G-T

122217207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 35984364-G-A

122217222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 35984379-A-T

122217230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 35984387-G-T

http://identifiers.org/hco/9/GRCh38#122217352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35984508-C-A

122217352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35984508-C-T

http://identifiers.org/hco/9/GRCh38#122217364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35984520-C-A

122217364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35984520-C-T

http://identifiers.org/hco/9/GRCh38#122217365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35984521-C-A

122217365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35984521-C-T

122217443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35984578-C-T

122217945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35985114-G-C

122217945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35985114-G-T

122217964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35985133-G-A

122218096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35985293-G-A

122218491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35985629-C-T

http://identifiers.org/hco/9/GRCh38#122218733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35985878-C-A

122218784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35985926-C-T

122218956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35986081-C-T

http://identifiers.org/hco/9/GRCh38#122219090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35986192-C-A

122219308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35986608-G-C

122219308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35986608-G-T

122219684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35986938-T-C

122219691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35986945-C-T

122220233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35987359-T-C

122220303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35987402-T-A

122220517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35987619-C-T

122220543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35987652-C-T

122220613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35987711-G-T

http://identifiers.org/hco/9/GRCh38#122220965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35988027-C-A

122220965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35988027-C-T

122220977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35988039-T-C

122221135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988188-A-G

122221172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988225-T-C

122221172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988225-T-G

122221195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988251-G-A

122221196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988252-G-A

122221196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988252-G-C

http://identifiers.org/hco/9/GRCh38#122221203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35988259-C-A

122221203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988259-C-T

http://identifiers.org/hco/9/GRCh38#122221236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35988310-C-A

122221255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988329-G-A

122221255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988329-G-T

http://identifiers.org/hco/9/GRCh38#122221372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35988448-C-A

122221372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988448-C-T

122221499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988565-G-A

122221499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988565-G-T

http://identifiers.org/hco/9/GRCh38#122221569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35988656-A-C

122221569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988656-A-G

http://identifiers.org/hco/9/GRCh38#122221570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35988657-C-A

122221570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988657-C-G

122221570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988657-C-T

122221599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988672-C-T

122221715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35988777-C-T

122221834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35988933-T-A

122222106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35989169-T-A

122222106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35989169-T-C

122222277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35989341-G-C

122222704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35989651-G-A

122222704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35989651-G-T

http://identifiers.org/hco/9/GRCh38#122222834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35989785-C-A

http://identifiers.org/hco/9/GRCh38#122223334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35990314-A-C

122223334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35990314-A-G

122223443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35990405-C-G

122223469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35990431-G-T

http://identifiers.org/hco/9/GRCh38#122223575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35990538-C-A

122223575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35990538-C-T

http://identifiers.org/hco/9/GRCh38#122223602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35990563-C-A

122223615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35990577-C-T

122223803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35990761-T-C

122224964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991491-C-T

122224980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991507-A-G

122224994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991517-C-G

122224994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991517-C-T

122225169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991666-G-A

122225192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991688-G-T

122225244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991754-T-C

122225325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991854-A-G

122225444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35991957-T-A

122225489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992008-C-T

122225530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992053-T-C

122225621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992148-C-G

122225843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992358-G-A

122225920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992435-C-T

122225957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992476-C-T

122226146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992644-G-A

122226146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992644-G-T

122226236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992725-G-A

122226236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992725-G-T

122226352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35992846-G-A

http://identifiers.org/hco/9/GRCh38#122226357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35992851-C-A

122226551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993045-G-A

122226551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993045-G-T

122226710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993207-G-A

122226710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993207-G-T

122226727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993233-G-A

122226727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993233-G-T

http://identifiers.org/hco/9/GRCh38#122226747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35993253-C-A

122226747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35993253-C-T

122226997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35993507-G-T

122227042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35993552-G-A

122227042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35993552-G-T

http://identifiers.org/hco/9/GRCh38#122227278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35993774-C-A

122227278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35993774-C-G

122227278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35993774-C-T

122227335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35993831-G-A

122227335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron variant
orthologous variants: 35993831-G-T

http://identifiers.org/hco/9/GRCh38#122227579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35994074-C-A

122227579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35994074-C-T

http://identifiers.org/hco/9/GRCh38#122228087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35994569-C-A

122228087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35994569-C-T

122228124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35994598-G-A

122228124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35994598-G-C

122228124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35994598-G-T

http://identifiers.org/hco/9/GRCh38#122228183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35994657-C-A

122228183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35994657-C-T

http://identifiers.org/hco/9/GRCh38#122228338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35994813-C-A

122228338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35994813-C-G

122228338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35994813-C-T

http://identifiers.org/hco/9/GRCh38#122228579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35995057-A-C

122228579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995057-A-T

122228647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995126-G-A

122228647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995126-G-C

122228647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995126-G-T

122228746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35995225-G-A

122228746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35995225-G-C

122228746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35995225-G-T

122228747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35995226-G-A

122228747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35995226-G-T

http://identifiers.org/hco/9/GRCh38#122228915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35995393-C-A

122228970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995448-G-A

122228970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995448-G-T

http://identifiers.org/hco/9/GRCh38#122229059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#35995552-C-A

122229059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995552-C-T

122229350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995829-A-G

122229350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35995829-A-T