43527847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660576-G-T

43527882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660610-T-C

43527915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660635-G-A

43527915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660635-G-C

http://identifiers.org/hco/17/GRCh38#43527969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101660660-C-A

http://identifiers.org/hco/17/GRCh38#43527989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101660678-A-C

43528001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660688-A-G

43528001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660688-A-T

43528012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660695-T-C

43528074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660748-G-A

43528074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660748-G-T

http://identifiers.org/hco/17/GRCh38#43528186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101660867-C-A

43528214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660890-T-A

43528214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660890-T-C

http://identifiers.org/hco/17/GRCh38#43528258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101660938-A-C

http://identifiers.org/hco/17/GRCh38#43528280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101660956-A-C

43528280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660956-A-G

43528283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660959-G-A

43528283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660959-G-C

43528283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660959-G-T

43528293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660969-A-G

43528311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660984-T-C

43528311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660984-T-G

43528314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101660991-G-T

http://identifiers.org/hco/17/GRCh38#43528323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101661000-C-A

http://identifiers.org/hco/17/GRCh38#43528327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101661004-C-A

43528327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101661004-C-T

43528367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101661043-G-A

43528439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101661114-G-T

43528591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 101661264-C-T

43528645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 101661318-C-T

43528779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661448-G-A

43528779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661448-G-C

43528782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661451-G-A

43528782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661451-G-T

43528811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661468-G-T

43528817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661474-G-A

http://identifiers.org/hco/17/GRCh38#43528867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101661527-C-A

43528867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661527-C-G

43528867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661527-C-T

http://identifiers.org/hco/17/GRCh38#43528868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101661528-C-A

43528880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661541-T-A

43528880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661541-T-C

43528880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661541-T-G

43528906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661564-T-G

43528955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661614-C-T

http://identifiers.org/hco/17/GRCh38#43529038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101661664-A-C

43529038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661664-A-T

43529064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661689-G-A

43529064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661689-G-T

43529074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661699-C-T

http://identifiers.org/hco/17/GRCh38#43529228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101661888-C-A

43529264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661930-G-A

43529270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101661936-A-G

http://identifiers.org/hco/17/GRCh38#43529338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101662003-A-C

43529338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662003-A-G

43529362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662020-G-A

43529362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662020-G-T

43529725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662363-C-G

43529725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662363-C-T

43529784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662411-A-G

43529805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662432-C-G

43530019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662652-G-A

43530019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662652-G-T

43530025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662658-C-G

43530043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101662678-C-G

43530271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662861-T-A

43530292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662882-T-C

http://identifiers.org/hco/17/GRCh38#43530308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101662898-C-A

43530308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662898-C-T

http://identifiers.org/hco/17/GRCh38#43530326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101662903-C-A

43530326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662903-C-T

43530393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662966-T-A

43530393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662966-T-C

43530406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 101662979-A-G

43530563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663130-A-G

43530574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663141-T-C

43530576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663143-A-G

43530577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663144-G-A

43530577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663144-G-C

43530577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663144-G-T

43530587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663154-T-G

43530609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663176-C-T

43530646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101663219-G-A

43532002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101664213-A-G

43532659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, undefined
orthologous variants: 101664417-A-G

http://identifiers.org/hco/17/GRCh38#43532715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101664476-A-C

http://identifiers.org/hco/17/GRCh38#43532814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101664575-C-A

43533303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 101665026-A-G

43533306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 101665029-G-A

43533439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101665162-A-T

43533594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101665892-T-C

43533753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666036-G-A

43533753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666036-G-T

43533935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 101666220-G-A

43533989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 101666274-T-C

43534047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666324-T-C

43534161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666427-A-G

43534585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666555-T-C

43535155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666801-A-G

43535215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666863-C-T

43535267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666926-G-A

43535299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101666962-A-G

43536020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667513-A-G

43536181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667668-T-C

http://identifiers.org/hco/17/GRCh38#43536184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101667671-C-A

43536236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667705-A-G

http://identifiers.org/hco/17/GRCh38#43536271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101667731-C-A

43536271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667731-C-G

43536271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667731-C-T

43536283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667745-T-A

43536283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667745-T-C

43536286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667748-A-G

43536287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667749-G-T

http://identifiers.org/hco/17/GRCh38#43536310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101667772-C-A

43536310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667772-C-G

43536310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667772-C-T

43536340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667825-G-T

http://identifiers.org/hco/17/GRCh38#43536400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101667887-C-A

43536400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667887-C-G

43536494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101667989-C-T

43536508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101668003-G-C

http://identifiers.org/hco/17/GRCh38#43536511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101668006-C-A

43536511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101668006-C-T

43536516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101668011-C-T

43536573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101668071-A-G

43539137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101669143-A-T

43539138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101669144-T-C

http://identifiers.org/hco/17/GRCh38#43539572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101669566-A-C

43540900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101670769-G-A

43540900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101670769-G-T

43541133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101670978-C-T

43541630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101671478-A-G

43541683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101671539-C-T

43541951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101671802-G-A

43542056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101671885-T-C

43542149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101671973-G-C

43542376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101672201-T-A

43542486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101672314-C-T

43542735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101672557-T-G

43542857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101672682-G-T

43543076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101672886-G-A

43543201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673002-T-C

43543201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673002-T-G

43543298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673106-A-T

http://identifiers.org/hco/17/GRCh38#43543354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101673172-C-A

43543354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673172-C-T

43543788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673600-T-A

http://identifiers.org/hco/17/GRCh38#43543861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101673674-C-A

43543864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673677-A-G

43543875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673688-C-T

43544043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673877-G-A

43544093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673933-T-G

43544099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101673939-G-T

http://identifiers.org/hco/17/GRCh38#43544162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101674002-C-A

43544162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 101674002-C-T

http://identifiers.org/hco/17/GRCh38#43544613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101674458-C-A

43544613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674458-C-G

43544613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674458-C-T

43544663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674509-T-G

http://identifiers.org/hco/17/GRCh38#43544670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101674516-C-A

http://identifiers.org/hco/17/GRCh38#43544837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101674696-C-A

43544926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674745-G-T

43544927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674746-T-A

43544927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674746-T-C

43544951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674770-A-G

43544980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674798-G-A

43545087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674899-C-G

43545087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101674899-C-T

43545239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675025-G-A

43545239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675025-G-T

43545250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675036-C-T

43545341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 101675123-G-T

http://identifiers.org/hco/17/GRCh38#43545472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101675256-C-A

43545472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675256-C-T

http://identifiers.org/hco/17/GRCh38#43545741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101675517-C-A

43546215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675964-G-A

43546215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675964-G-T

43546245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675997-A-G

http://identifiers.org/hco/17/GRCh38#43546247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
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/11/GRCm39#101675999-C-A

43546247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675999-C-T

43546269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676021-G-A

43546269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676021-G-T

43546482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676231-G-T

43546486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676235-G-C

43546486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676235-G-T

43546520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676269-G-A

43546520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676269-G-T

http://identifiers.org/hco/17/GRCh38#43546521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101676270-C-A

43546521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676270-C-T

43546650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676401-G-A

43546978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676745-G-A

43547002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676770-C-T

43547056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101676811-C-G

43547870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101677417-G-T

43547986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101677513-G-A

43549064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101678044-G-C

43549293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101678237-A-T

43549296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101678240-C-T

43549312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101678248-A-G

43549644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101678485-A-T

43549713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101678554-A-G

43550104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101679412-T-C

43550137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101679446-T-C

43550152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101679451-G-A

43550152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101679451-G-C

43550230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101679567-T-C

43550325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101679672-C-T

43552457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101681938-T-C

43552533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682015-G-A

43552674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682156-C-T

43552800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682268-G-A

43553401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682460-A-G

43553513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682551-G-T

43553518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682571-C-T

http://identifiers.org/hco/17/GRCh38#43553526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101682579-C-A

43553526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682579-C-T

43553555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682608-C-T

43553579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682670-T-C

43553924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682920-G-A

43553951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101682947-T-C

http://identifiers.org/hco/17/GRCh38#43554802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101684281-C-A

43554933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101684397-A-G

43555097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101684545-C-T

http://identifiers.org/hco/17/GRCh38#43560067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101688846-C-A

43560315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101689115-G-A

43562522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101690863-A-G

43562536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101690876-G-A

43562935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101692310-C-T

43563249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101692627-A-G

43563950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101693304-G-A

43563967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101693321-T-A

43564266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101695302-G-C

43564268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101695304-T-C

43564765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101695749-A-G

43569184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101697465-T-C

43569310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101697590-G-A

43569424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101697713-G-T

43569726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101697969-A-G

43570840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101698415-G-T

43572440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101698603-A-T

43572649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101698792-T-C

43573426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101699882-G-A

43573673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101700061-T-C

http://identifiers.org/hco/17/GRCh38#43574051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101700450-C-A

43574178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101700556-T-C

http://identifiers.org/hco/17/GRCh38#43574352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101700791-C-A

43574352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101700791-C-T

43574965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101701459-G-T

http://identifiers.org/hco/17/GRCh38#43575241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101701710-C-A

43575696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101702252-T-C

43575865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101702427-G-A

43575865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101702427-G-C

43576134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101702796-C-T

43576139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101702801-C-T

43576169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101702828-G-A

43576661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101703791-G-A

43576865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101704320-C-T

43576968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101704438-G-A

43576975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101704445-C-T

43577049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101704520-C-T

43577116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101704646-G-A

43577192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101704765-A-G

43577686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101705367-T-C

43578258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101705906-G-A

43578442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706077-G-A

43579152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706770-G-T

43579155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706773-A-G

http://identifiers.org/hco/17/GRCh38#43579162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101706780-C-A

43579162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706780-C-G

43579162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706780-C-T

http://identifiers.org/hco/17/GRCh38#43579265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101706846-C-A

43579265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706846-C-T

43579385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706920-G-A

43579385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706920-G-T

43579412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101706963-T-C

http://identifiers.org/hco/17/GRCh38#43579482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101707031-C-A

43579482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101707031-C-T

http://identifiers.org/hco/17/GRCh38#43579564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101707102-C-A

http://identifiers.org/hco/17/GRCh38#43579566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3493
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#101707104-C-A