http://identifiers.org/hco/6/GRCh38#75084327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79506274-C-A

75084418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79506365-T-G

75084638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79506592-C-T

http://identifiers.org/hco/6/GRCh38#75084814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79506763-A-C

75084932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79506863-G-A

75084932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79506863-G-T

http://identifiers.org/hco/6/GRCh38#75085029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79506956-C-A

75085075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79507003-G-C

75085075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79507003-G-T

http://identifiers.org/hco/6/GRCh38#75085130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79507061-C-A

75085130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79507061-C-G

75085133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79507064-T-A

75085136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79507067-A-G

75085259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79507180-C-G

75085259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79507180-C-T

75085280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 79507204-G-C

75085280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 79507204-G-T

75085325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79507249-G-C

75085325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79507249-G-T

75085455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507373-G-A

75085455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507373-G-C

75085455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507373-G-T

http://identifiers.org/hco/6/GRCh38#75085457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79507375-A-C

http://identifiers.org/hco/6/GRCh38#75085777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79507703-C-A

75085778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507704-G-A

75085778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507704-G-T

75085856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507775-T-C

http://identifiers.org/hco/6/GRCh38#75085876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79507794-C-A

75085876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507794-C-T

http://identifiers.org/hco/6/GRCh38#75085896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79507814-C-A

75085974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79507890-G-T

http://identifiers.org/hco/6/GRCh38#75085987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79507903-A-C

75086148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508068-C-T

75086247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508165-C-T

75086282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508200-T-C

75086287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508203-G-T

75086544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508448-G-A

75086544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508448-G-C

75086544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79508448-G-T

75086617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79508528-T-A

75086993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79508894-C-T

75087128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79509025-G-A

75087128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79509025-G-T

75087280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509196-A-T

75087281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509197-G-A

75087281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509197-G-T

75087315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509239-A-G

75087316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509240-G-C

75087316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509240-G-T

75087457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509380-G-T

http://identifiers.org/hco/6/GRCh38#75087490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79509413-C-A

75087490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509413-C-T

75087550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79509455-G-A

75087771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79509701-T-C

75087802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79509730-G-A

75087817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79509751-T-A

http://identifiers.org/hco/6/GRCh38#75087828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79509762-C-A

75087828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79509762-C-T

http://identifiers.org/hco/6/GRCh38#75088305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79510292-C-A

75088320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79510310-G-A

http://identifiers.org/hco/6/GRCh38#75088457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79510418-C-A

http://identifiers.org/hco/6/GRCh38#75088469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79510431-C-A

75089712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511229-C-G

75089924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511419-A-G

75090014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511541-T-G

75090055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511583-T-A

75090305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79511870-G-A

75090305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79511870-G-C

75090428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79511959-T-C

75090428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79511959-T-G

75090588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79512114-G-A

http://identifiers.org/hco/6/GRCh38#75091603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79512946-C-A

75091603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79512946-C-T

75091619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79512962-T-C

75091633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79512976-G-A

75091633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79512976-G-T

75091916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79513209-T-C

75093724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79513903-T-C

75094486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79514606-T-C

75094487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79514607-G-A

http://identifiers.org/hco/6/GRCh38#75094958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79515555-C-A

75094958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515555-C-T

http://identifiers.org/hco/6/GRCh38#75095014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79515611-C-A

75095021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515618-A-G

75095062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515660-T-C

75095095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515692-G-A

75095095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515692-G-C

75095095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515692-G-T

75095117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79515711-A-G

75095175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 79515769-C-G

75095175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 79515769-C-T

75095196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515789-G-A

75095196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515789-G-C

75095204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515797-G-A

75095204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515797-G-T

75095246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515843-T-C

http://identifiers.org/hco/6/GRCh38#75095846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79516085-C-A

75095846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516085-C-T

75096481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516690-C-T

75097053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516911-A-T

75097210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517060-G-A

75097210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517060-G-T

75097212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517062-G-A

75097212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517062-G-T

75097223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517071-G-A

75097223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517071-G-T

75097233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517076-G-A

75097233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517076-G-T

http://identifiers.org/hco/6/GRCh38#75097256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79517099-C-A

75097256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79517099-C-T

75097263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79517106-G-A

75097263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79517106-G-C

75097312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79517155-G-T

75097349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517189-G-A

75097349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517189-G-C

75097349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517189-G-T

75097431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517267-G-A

75097436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517272-G-A

75097436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517272-G-T

http://identifiers.org/hco/6/GRCh38#75097465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79517311-A-C

75097526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517373-A-T

75097565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79517411-C-T

http://identifiers.org/hco/6/GRCh38#75097598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79517444-A-C

75097838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516228-T-C

75097959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516347-A-G

75098062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516447-T-C

75098132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516507-G-A

75098132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516507-G-T

75098208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516585-C-T

75098951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79517815-C-T

75099429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79518370-G-T

75099680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79518606-C-T

75099711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79518642-T-C

75099978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79518816-C-G

75100266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519112-G-T

75100409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519248-G-A

75100409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519248-G-T

75100489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519325-A-G

http://identifiers.org/hco/6/GRCh38#75100641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79519469-C-A

75100699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519525-A-G

75101462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519570-A-G

75101464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519572-A-G

75101484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519584-G-T

75101490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519590-C-T

http://identifiers.org/hco/6/GRCh38#75101498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79519598-A-C

75101498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519598-A-G

75101498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519598-A-T

75101523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519634-T-A

75101700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519778-G-T

75101747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79519834-A-G

75101853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79519936-G-A

75101853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79519936-G-T

75101896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79519979-T-C

75101898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79519981-C-G

75101914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79519996-T-C

75101930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520012-A-G

http://identifiers.org/hco/6/GRCh38#75101938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79520131-A-C

75101978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520180-G-A

75101978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520180-G-T

http://identifiers.org/hco/6/GRCh38#75102153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79520349-C-A

75102153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520349-C-T

75102161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520357-A-G

http://identifiers.org/hco/6/GRCh38#75102178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79520375-C-A

75102178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520375-C-G

75102178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520375-C-T

75102243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520440-C-T

75102248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520445-G-A

75102481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520662-A-G

75102481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520662-A-T

75102512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520690-T-G

75102513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520691-T-A

75102513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520691-T-C

75102547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79520992-T-C

75102557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521003-T-A

75102603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521049-T-A

75102603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521049-T-C

75102624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521070-G-A

75102624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521070-G-T

75102651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521097-G-A

75102651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521097-G-T

75102708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521155-G-A

75102708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521155-G-C

75102708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521155-G-T

75102711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521158-A-G

75102763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521213-A-G

75102770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521220-A-G

75102783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521233-G-A

75102783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521233-G-T

http://identifiers.org/hco/6/GRCh38#75102790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79521239-A-C

http://identifiers.org/hco/6/GRCh38#75102820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79521269-C-A

75102820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521269-C-T

http://identifiers.org/hco/6/GRCh38#75102826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79521275-C-A

75102826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521275-C-T

75102934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521397-T-A

http://identifiers.org/hco/6/GRCh38#75103016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79521470-A-C

75103626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521512-T-G

75103645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521530-A-G

http://identifiers.org/hco/6/GRCh38#75103654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79521539-C-A

75103656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521541-G-A

75103799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521673-A-G

75103799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79521673-A-T

75103839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521717-G-A

75103839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521717-G-T

75103899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521777-T-C

http://identifiers.org/hco/6/GRCh38#75103942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79521821-C-A

75103942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521821-C-T

75103953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79521832-T-C

http://identifiers.org/hco/6/GRCh38#75104133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79522044-C-A

75104266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522168-C-T

75104281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522183-G-A

75104445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522308-T-C

75104599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522470-G-A

75104625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522503-A-G

75104714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522591-G-A

75104814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79522705-G-C

75105070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523155-T-C

75105072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523157-G-A

75105072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523157-G-T

75105137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523225-A-G

75105137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523225-A-T

http://identifiers.org/hco/6/GRCh38#75105194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79523293-C-A

75105194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523293-C-T

75105245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79523344-T-C

75105272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79523371-A-G

75105316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523415-A-T

http://identifiers.org/hco/6/GRCh38#75105381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79523483-C-A

75105383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523485-G-T

75105586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523691-T-C

75105669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523904-G-C

75105669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523904-G-T

75105679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79523914-A-G

75105917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524501-C-T

75106029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524597-T-C

75106029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524597-T-G

http://identifiers.org/hco/6/GRCh38#75106040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79524608-A-C

75106044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524612-G-T

75106309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524876-G-T

75106380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524948-T-A

75106380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524948-T-C

75106384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79524952-A-T

http://identifiers.org/hco/6/GRCh38#75106584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79525243-C-A

75106584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79525243-C-T

75106742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79525392-G-A

75108829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527037-C-G

75108852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527065-T-A

http://identifiers.org/hco/6/GRCh38#75108944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79527148-C-A

75108944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527148-C-G

http://identifiers.org/hco/6/GRCh38#75108967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79527166-C-A

75108967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527166-C-T

75108968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527167-A-G

75108969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527168-T-C

75109007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527212-G-A

75109007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527212-G-C

75109021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79527226-G-A

75109063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79527268-A-G

75109180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527385-T-C

75109214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527417-A-G

75109214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527417-A-T

75109284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527607-A-T

75109365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527680-T-C

75109437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527749-C-T

75109574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527890-C-T

75109636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527926-A-G

75109659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79527950-T-G

75109867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79528149-T-C

75109910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79528191-A-G

75110382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79528641-T-A

75110434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79528692-A-G

75110454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79528711-G-C

75110454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79528711-G-T

75111267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79530322-G-A

http://identifiers.org/hco/6/GRCh38#75112509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79533389-C-A

75112510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79533390-T-A

75112520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79533394-A-G

75112613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79533479-A-G

75112885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79533716-G-T

http://identifiers.org/hco/6/GRCh38#75112989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79533988-C-A

http://identifiers.org/hco/6/GRCh38#75113081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79534151-C-A

75113081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79534151-C-T

75113160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79534226-T-A

75113160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79534226-T-C

http://identifiers.org/hco/6/GRCh38#75113169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79534236-C-A

75113169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79534236-C-T

75113182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79534249-T-C

75113225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: 79534292-T-A

75113270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79534337-G-A

75113270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79534337-G-C

75113270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79534337-G-T

75113309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79534376-A-G

75113317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79534384-T-A

75113317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79534384-T-C

75113342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79534412-T-C

http://identifiers.org/hco/6/GRCh38#75113498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79535543-C-A

http://identifiers.org/hco/6/GRCh38#75113509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79535554-A-C

http://identifiers.org/hco/6/GRCh38#75113525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79535571-C-A

75113525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79535571-C-T

http://identifiers.org/hco/6/GRCh38#75113582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79535623-C-A

75113696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79535743-T-C

75113720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79535767-A-G

75113720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79535767-A-T

75113764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79535813-A-G

75113771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79535820-A-G

75113838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79535843-T-C

75113838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79535843-T-G

75114102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536062-T-C

75114214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536179-G-C

http://identifiers.org/hco/6/GRCh38#75114255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79536215-C-A

75114608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536542-T-C

75114608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536542-T-G

75114707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536656-T-C

75114753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536717-A-G

75114822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536773-A-G

75114892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536843-C-T

75114952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536893-G-A

75115055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79536989-G-T

75115191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537124-C-T

75115274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537208-G-T

75115295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537229-A-T

75115334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537267-A-G

75115366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537299-C-G

75115468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537411-G-A

75115579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537560-G-A

75115582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537563-G-A

75115618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537599-T-C

http://identifiers.org/hco/6/GRCh38#75115667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79537646-C-A

75115667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537646-C-T

75115744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79537723-A-G

75116117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538094-C-T

75116142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538119-T-C

75116148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538125-A-T

http://identifiers.org/hco/6/GRCh38#75116164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79538145-C-A

75116936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538369-A-G

75117131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538529-G-A

75117332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538726-T-C

75117355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538743-T-C

http://identifiers.org/hco/6/GRCh38#75117356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79538744-A-C

75117373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538761-G-A

75117392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79538780-A-G

75117473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79538861-A-G

75117503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79538891-A-G

75117556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538943-A-G

75117590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538975-T-A

75117590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538975-T-C

75117591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538976-G-T

75117602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538988-T-A

75117602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79538988-T-C

75117629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79539033-G-A

75117629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79539033-G-T

http://identifiers.org/hco/6/GRCh38#75117658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79539062-C-A

75117658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79539062-C-T

75117721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79539144-T-C

75117985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79539384-C-T

75118392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540012-A-G

75118844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540465-A-G

75118986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540569-G-A

75118991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540574-C-T

75118999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540582-A-G

http://identifiers.org/hco/6/GRCh38#75119005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79540586-A-C

75119112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79540693-A-G

75119140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79540721-G-A

75119204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540784-G-A

75119264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79540837-T-C

75119414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79540974-A-G

75119476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79541036-G-A

75119587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541125-A-T

http://identifiers.org/hco/6/GRCh38#75119597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79541135-A-C

75119621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541151-T-G

75119683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541213-G-C

75119703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541411-T-C

75119842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541555-G-A

75119895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541604-G-A

75120017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541718-G-C

75120151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79541863-T-A

75120786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542130-G-A

75120887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542230-T-C

75121057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542371-G-C

http://identifiers.org/hco/6/GRCh38#75121126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79542440-C-A

75121126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542440-C-T

75121189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542501-T-C

75121191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542503-G-A

75121191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542503-G-C

75121191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542503-G-T

75121217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542528-T-C

http://identifiers.org/hco/6/GRCh38#75121248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79542594-C-A

75121248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542594-C-G

75121248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542594-C-T

http://identifiers.org/hco/6/GRCh38#75121287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79542657-C-A

75121287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542657-C-T

75121401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79542771-A-G

http://identifiers.org/hco/6/GRCh38#75121505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79542873-C-A

75121506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79542874-A-G

75121803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79544197-A-G

75121857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79544247-C-T

75122392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79544519-G-C

75122485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79544593-G-A

75123100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545509-C-T

75123140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545549-A-G

75123436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545832-C-G

75123436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545832-C-T

75123466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545865-T-A

75123499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545886-A-G

75123540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545926-T-C

75123545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79545930-T-C

75123685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79546066-C-G

75123800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79546859-G-A

75123869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79546903-G-A

75123869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79546903-G-T

http://identifiers.org/hco/6/GRCh38#75123882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79546908-C-A

75123882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79546908-C-T

75124090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79547096-T-C

75124090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79547096-T-G

75124207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547209-G-A

75124207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547209-G-C

75124230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547226-A-G

75124230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547226-A-T

75124402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547399-T-C

75124404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547401-G-A

75124404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547401-G-T

75124445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547445-T-A

75124487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547496-T-C

http://identifiers.org/hco/6/GRCh38#75124540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79547549-C-A

75124593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547773-T-C

75124641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547812-T-A

75124721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79547889-A-G

75124854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79548109-A-G

http://identifiers.org/hco/6/GRCh38#75125013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79548372-C-A

75125013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79548372-C-T

http://identifiers.org/hco/6/GRCh38#75125033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79548642-C-A

75125033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79548642-C-T

75125084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79548691-T-C

75125191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79548795-A-G

75125191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: 79548795-A-T

75125304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79548905-A-G

75125358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79548959-G-T

75125487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549077-G-A

75125514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549103-A-G

75125696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549283-C-T

75125704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549291-A-T

75125797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549374-A-G

75125898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549438-A-T

75126148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79549654-A-G

75126317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551115-A-G

75126499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551297-G-T

75126559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551316-A-G

75126559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551316-A-T

http://identifiers.org/hco/6/GRCh38#75126580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79551342-C-A

75126671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551429-T-C

75126685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551443-A-G

75126737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551486-G-C

75126801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551544-T-C

http://identifiers.org/hco/6/GRCh38#75127005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79551761-A-C

75127072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551824-A-G

75127202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79551944-A-G

75127589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552289-G-A

http://identifiers.org/hco/6/GRCh38#75127704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79552396-C-A

75127707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552399-A-G

75127711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552403-G-T

75127727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552409-C-T

75127802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552485-T-C

75127879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552535-G-A

75127920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552576-C-T

http://identifiers.org/hco/6/GRCh38#75128074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79552719-C-A

75128158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552800-T-C

75128270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552915-T-C

75128272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79552917-A-G

75128355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: 79553003-G-A

75128355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: 79553003-G-T

75128500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553149-T-C

75128503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553152-T-G

75128540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553180-T-G

75128560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553200-T-C

75128605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553245-T-C

75128718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79553363-G-C

75128742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79553380-A-G

75128769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79553393-A-T

75128942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553533-G-A

75128998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553596-C-T

75129093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553679-T-C

75129093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553679-T-G

75129225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553785-A-G

75129355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553915-G-A

75129427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553988-T-C

75129427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79553988-T-G

75129616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79554419-C-T

75129697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79554498-G-A

75129758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79554555-C-T

75130007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79554781-A-G

http://identifiers.org/hco/6/GRCh38#75130041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79554809-C-A

75130041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79554809-C-G

75130041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79554809-C-T

75130217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79554987-T-G

http://identifiers.org/hco/6/GRCh38#75130265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79555031-C-A

75130265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555031-C-T

75130335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555098-G-A

75130335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555098-G-C

75130335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555098-G-T

75130351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555113-T-A

75130497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555278-T-C

75130662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555739-G-A

75130662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79555739-G-T

75130910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79556001-G-A

75130910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: 79556001-G-T

75131262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79556320-C-T

75131291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79556348-T-G

75131852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557011-G-T

http://identifiers.org/hco/6/GRCh38#75132009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79557253-A-C

75132027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79557271-G-A

75132027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79557271-G-C

75132115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557359-A-T

75132183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557428-G-A

75132289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557514-C-T

75132405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557625-T-A

75132405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557625-T-C

75132438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79557765-A-G

http://identifiers.org/hco/6/GRCh38#75132954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79558488-A-C

75132954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558488-A-G

75133232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558607-G-A

75133232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558607-G-T

75133248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558623-G-A

75133248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558623-G-T

75133294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 79558665-T-C

75133294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 79558665-T-G

75133357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79558728-A-G

75133396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79558767-A-G

75133396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: stop gained
orthologous variants: 79558767-A-T

75133411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79558782-G-A

75133411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79558782-G-C

75133411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79558782-G-T

75133693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558985-A-G

75133699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79558991-G-T

75133815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79559095-C-G

75133878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: 79559237-C-T

75134097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79559455-G-A

75134097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79559455-G-T

http://identifiers.org/hco/6/GRCh38#75134106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79559464-C-A

75134106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79559464-C-G

75134106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79559464-C-T

75134703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79560573-A-G

75135101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79560967-C-T

75135390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79561245-G-T

75135566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79561421-C-G

75135566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79561421-C-T

75135705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79561570-T-C

75135770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79561645-G-A

75135893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79561767-T-C

75136633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562098-G-C

75136664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562124-G-A

75136714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562172-T-C

75136833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562247-G-A

75136835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562249-T-A

75136845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562259-A-G

75137142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562443-T-C

75137142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562443-T-G

75137282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562535-G-C

75137670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562941-T-A

75137670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562941-T-C

http://identifiers.org/hco/6/GRCh38#75137674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79562945-C-A

75137674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562945-C-G

75137674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562945-C-T

75137704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562975-T-A

75137715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562978-G-T

75137721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562984-G-T

75137731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562994-T-C

75137731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79562994-T-G

75137825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79563081-G-A

75138209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79563758-C-T

75138213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79563762-G-T

75138303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79563844-T-A

75138434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79563980-A-T

75138452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79563998-G-A

75138452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79563998-G-T

75138621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79564165-G-A

http://identifiers.org/hco/6/GRCh38#75138759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79564411-A-C

http://identifiers.org/hco/6/GRCh38#75138806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79564564-A-C

75138855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79564615-A-G

75138915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79564675-T-C

75138965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79564725-T-A

75138965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79564725-T-C

75138978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79564738-C-T

75139024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79564781-T-A

75139024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79564781-T-C

75139077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79564833-C-T

75139081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79564837-G-T

75139213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79565011-C-T

75139281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79565070-T-C

75139923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79566810-G-C

75139930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79566817-A-G

75139970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79566861-A-G

75140135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567020-G-T

75140291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567137-A-G

http://identifiers.org/hco/6/GRCh38#75140295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79567141-C-A

75140295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567141-C-T

75140610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567293-C-T

75140847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567397-A-G

75140856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567407-G-A

75140983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567511-A-G

75140986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567513-G-A

http://identifiers.org/hco/6/GRCh38#75141318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79567808-C-A

75141488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79567943-C-T

http://identifiers.org/hco/6/GRCh38#75141899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79568138-A-C

75141902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568141-A-G

75141964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568201-G-T

75141982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568219-G-T

75141985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568222-T-C

75141986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568223-G-A

75141988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568225-A-G

75142033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 79568267-G-C

75142045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79568279-A-G

75142159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 79568393-T-C

75142212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568445-G-T

75142239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568472-G-T

75142245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568478-G-A

75142245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568478-G-C

75142252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568485-T-C

75142274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568508-A-G

http://identifiers.org/hco/6/GRCh38#75142302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79568535-C-A

75142312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568545-G-A

75142312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568545-G-C

75142313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568546-A-G

75142313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568546-A-T

75142371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568603-A-G

75142396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568629-C-T

75142403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79568636-A-G

75142770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79569232-G-A

75142770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79569232-G-C

75142840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79569325-C-G

75143324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79569814-A-G

75144006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79578590-C-T

75144158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79578749-G-A

75144174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79578765-A-G

75144351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79578932-T-A

75144365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79578946-T-C

http://identifiers.org/hco/6/GRCh38#75144628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79579137-A-C

75144753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79579256-C-T

75144817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79579320-T-C

http://identifiers.org/hco/6/GRCh38#75144916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79579402-C-A

75145139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79579963-G-A

http://identifiers.org/hco/6/GRCh38#75145255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79580139-C-A

75145384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79580244-T-A

75145384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79580244-T-C

75145438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79580298-T-C

75145447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79580307-C-T

75145537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580394-A-T

http://identifiers.org/hco/6/GRCh38#75145983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79580506-A-C

75145983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580506-A-G

75146066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580603-G-T

75146277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79580812-G-A

75146277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79580812-G-C

75146308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79580829-G-A

75146308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79580829-G-T

http://identifiers.org/hco/6/GRCh38#75146327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79580845-A-C

75146327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79580845-A-G

http://identifiers.org/hco/6/GRCh38#75146391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79580910-C-A

http://identifiers.org/hco/6/GRCh38#75146400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79580917-A-C

75146448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79580962-C-T

http://identifiers.org/hco/6/GRCh38#75147703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79581367-A-C

75147703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79581367-A-G

75147745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79581409-T-C

75147871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581520-A-G

http://identifiers.org/hco/6/GRCh38#75147872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79581521-C-A

75147872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581521-C-G

75147872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581521-C-T

75147886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581534-G-A

75147886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581534-G-T

http://identifiers.org/hco/6/GRCh38#75147920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79581564-A-C

75147920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581564-A-G

75147974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581617-T-C

http://identifiers.org/hco/6/GRCh38#75148184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79581816-A-C

75148203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581835-C-T

75148237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581862-G-T

75148268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581874-G-T

http://identifiers.org/hco/6/GRCh38#75148270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79581876-C-A

75148270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79581876-C-T

75148500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79582105-A-T

75148536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582138-T-C

75148536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582138-T-G

75148538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582140-G-A

75148555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582157-T-C

75148555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582157-T-G

75148618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582217-A-G

75148691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582286-G-T

75148711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582307-T-C

75148725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582321-C-T

http://identifiers.org/hco/6/GRCh38#75149196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79582429-C-A

75149348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582538-G-T

75149590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582764-T-C

75149597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582771-A-G

75149818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79582974-C-T

75149866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583027-T-G

75150125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583292-A-G

75150126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583293-A-G

75150141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583308-A-T

75150307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583470-C-T

75150359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583520-T-C

75150362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583523-C-T

75150407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583570-C-T

http://identifiers.org/hco/6/GRCh38#75150416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79583579-C-A

http://identifiers.org/hco/6/GRCh38#75150421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79583584-C-A

75150612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583745-A-G

75150682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583829-G-A

75150698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79583845-G-A

75152258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79585669-G-T

75152270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79585681-A-G

75152286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79585697-G-A

http://identifiers.org/hco/6/GRCh38#75152298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79585709-A-C

75152412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: synonymous variant
orthologous variants: 79585822-C-G

http://identifiers.org/hco/6/GRCh38#75152503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79585913-C-A

75152509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79585919-A-G

75152715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586081-T-C

75152715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586081-T-G

75152724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586090-C-G

75152909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586273-T-G

75152957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586320-A-G

75153064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586424-C-T

75153419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586784-A-G

75153499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586858-C-T

75153514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586873-T-C

75153535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586894-A-G

75153567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79586923-G-A

75153694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587044-C-T

75153837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587189-T-C

75153920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587280-T-G

75154398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587557-T-C

75154406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587565-A-G

75154406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587565-A-T

75154408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79587567-T-C

75154576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587731-T-C

75154828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79587965-T-C

75154883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588018-G-A

http://identifiers.org/hco/6/GRCh38#75155094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79588223-A-C

75155320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588436-C-T

75155359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588475-A-T

75155583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588613-G-T

75155835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79588844-A-G

75155898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588908-G-A

75155898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588908-G-C

75155898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588908-G-T

75155918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588928-A-G

75155963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79588973-G-T

http://identifiers.org/hco/6/GRCh38#75155969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79588982-C-A

75155996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589010-G-A

75156005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589019-G-A

75156005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589019-G-T

75156129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589144-G-T

75156189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589218-G-C

75156189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589218-G-T

75156193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589222-T-A

75156193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589222-T-C

75156216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589255-T-G

http://identifiers.org/hco/6/GRCh38#75156218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79589257-A-C

75156218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589257-A-G

75156218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589257-A-T

75156222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589261-T-C

75156336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79589383-T-C

75156680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589753-G-C

75156718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79589791-C-T

http://identifiers.org/hco/6/GRCh38#75156743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79589816-A-C

75157302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79590357-T-C

75165244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591243-A-G

75165293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591295-G-T

75165425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591393-G-C

75165447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591415-G-C

75165496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591465-A-G

http://identifiers.org/hco/6/GRCh38#75165640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79591609-C-A

75165655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79591624-A-G

75165661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79591630-A-G

75165729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant
orthologous variants: 79591698-T-A

75165729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant
orthologous variants: 79591698-T-C

75165760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79591729-A-G

75165763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79591732-T-C

75165792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591761-T-C

75165815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591783-A-G

75165815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591783-A-T

75165848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591811-G-T

75165854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591817-G-A

75165854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591817-G-C

75165854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591817-G-T

75165891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79591854-G-T

http://identifiers.org/hco/6/GRCh38#75165895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79591858-A-C

75166106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79592058-T-C

75166161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79592113-G-A

http://identifiers.org/hco/6/GRCh38#75166641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79592599-C-A

75167320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79593211-A-T

75167633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79593521-T-A

75167633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79593521-T-C

http://identifiers.org/hco/6/GRCh38#75167911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79593799-C-A

75168123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79593998-C-T

75168198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79594202-A-T

75168277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79594299-A-G

75168303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79594324-C-T

75168461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79594482-G-T

75168875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79594936-A-G

75168986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79595025-C-T

75169045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79595093-G-A

75170329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79596734-T-C

75170388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79596795-G-T

75170587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79596969-G-A

75171463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79597861-T-A

75171466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79597864-A-G

75171536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79597926-G-A

75171750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598136-G-A

75171838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598224-A-G

75172005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598374-G-A

75172141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598523-G-C

75172156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598544-T-A

75172156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598544-T-C

75172156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79598544-T-G

75174591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79599085-G-A

http://identifiers.org/hco/6/GRCh38#75174882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79599296-A-C

75174938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79599355-T-C

75174938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79599355-T-G

http://identifiers.org/hco/6/GRCh38#75175024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79599428-A-C

75175024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79599428-A-T

75175031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79599435-T-C

75175031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79599435-T-G

75175201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79599605-G-A

75175414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79599837-A-G

75177688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79600671-T-C

http://identifiers.org/hco/6/GRCh38#75177690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79600673-A-C

75177690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79600673-A-G

75177813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79600796-C-T

75177916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79600899-G-A

75177916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79600899-G-T

75178639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79601305-C-T

75180873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79604618-A-G

75180994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79604738-C-T

http://identifiers.org/hco/6/GRCh38#75181080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79604824-C-A

75181080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79604824-C-T

75181093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79604837-A-G

75181218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79604962-A-G

75181218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79604962-A-T

75181436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79605154-A-G

75181437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79605155-C-T

75182708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79606116-C-T

75182766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79606171-A-G

http://identifiers.org/hco/6/GRCh38#75182883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79606283-A-C

75182949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79606398-C-T

75182951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79606400-T-C

75182952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79606401-G-A

75182952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79606401-G-T

http://identifiers.org/hco/6/GRCh38#75183114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79606595-A-C

75183240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 79606721-T-C

75183333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 79606814-T-A

75183624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79607105-G-A

75183699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607192-T-A

75183699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607192-T-C

75183717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607220-G-A

75183717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607220-G-T

75183730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607233-G-T

75183900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79607585-T-C

75184140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79607825-A-G

75184140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79607825-A-T

75184224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607917-A-G

75184244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79607937-T-A

75187913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79608692-C-T

75188010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79608803-A-G

75188214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79609381-G-T

75188229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79609394-A-T

75188265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79609409-G-A

75188265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79609409-G-C

75188265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79609409-G-T

75188417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79609563-G-A

75188548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79609694-A-G

75188548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79609694-A-T

75188571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79609718-G-A

75188652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79609797-C-G

75188929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79610298-G-A

75188964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79610333-T-G

75189079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79610452-T-A

75189147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79610511-T-C

75189180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79610543-G-C

75189180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79610543-G-T

http://identifiers.org/hco/6/GRCh38#75189865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79611219-A-C

http://identifiers.org/hco/6/GRCh38#75189867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79611229-C-A

75189928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79611270-T-A

75189936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79611278-T-C

75190080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79611413-G-T

75190121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79611454-C-T

http://identifiers.org/hco/6/GRCh38#75190612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79611896-A-C

75191261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612564-T-C

75191525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612676-A-G

75191604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612751-G-A

75191604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612751-G-C

75191604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612751-G-T

75191681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612826-A-G

75191776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612919-A-G

75191776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612919-A-T

75191777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612920-T-C

75191854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79612977-G-T

75191897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613015-G-A

75191897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613015-G-T

75191903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613021-T-A

75191959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613077-G-T

http://identifiers.org/hco/6/GRCh38#75192065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79613136-C-A

75192083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613154-G-T

http://identifiers.org/hco/6/GRCh38#75192088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79613159-C-A

75192088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613159-C-G

75192088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613159-C-T

75192288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 79613586-A-G

http://identifiers.org/hco/6/GRCh38#75192481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79613775-C-A

75192481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613775-C-T

http://identifiers.org/hco/6/GRCh38#75192500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79613794-C-A

75192543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79613838-G-A

http://identifiers.org/hco/6/GRCh38#75193099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79614198-A-C

75193099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79614198-A-G

http://identifiers.org/hco/6/GRCh38#75193462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79614728-C-A

75194281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79614873-A-G

75194761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79615033-G-A

75194761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79615033-G-T

http://identifiers.org/hco/6/GRCh38#75195006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79615273-A-C

75195802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79616047-A-G

http://identifiers.org/hco/6/GRCh38#75197060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79617310-C-A

75197206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron variant
orthologous variants: 79617454-A-T

http://identifiers.org/hco/6/GRCh38#75198055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79617949-A-C

75198587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79618264-C-T

75198720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79618454-G-A

75199446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79619821-T-C

75199525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79619890-A-G

http://identifiers.org/hco/6/GRCh38#75199709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79620081-C-A

75200001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620330-G-A

75200069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620403-T-C

75200086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620417-C-T

75200370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620665-C-T

75200769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620812-T-C

75200935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620948-G-A

75200935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620948-G-T

http://identifiers.org/hco/6/GRCh38#75200966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79620981-C-A

75200966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79620981-C-T

75201675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79621597-C-T

75201852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79621756-G-C

75201956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79621867-G-A

http://identifiers.org/hco/6/GRCh38#75202101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79622007-C-A

http://identifiers.org/hco/6/GRCh38#75202153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79622075-C-A

75202312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79622251-G-A

75202366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79622301-C-T

75202578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79622510-G-A

75202578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79622510-G-T

http://identifiers.org/hco/6/GRCh38#75202904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79622828-C-A

75203046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79622969-G-A

75203191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79623112-G-A

http://identifiers.org/hco/6/GRCh38#75203433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79623387-C-A

75203847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79623796-G-A

75203891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79623840-T-G

75204144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79624093-G-T

75204503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79624471-T-C

75204685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79624647-G-A

75204983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79624953-G-A

75205095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79625063-A-G

75205172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79625142-G-C

75205309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79625240-G-A

http://identifiers.org/hco/6/GRCh38#75205380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79625326-C-A

75205380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79625326-C-T

http://identifiers.org/hco/6/GRCh38#75205669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79625583-C-A

75205669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79625583-C-T

http://identifiers.org/hco/6/GRCh38#75205783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#79625707-C-A

75205783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79625707-C-G

75205783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79625707-C-T

75205890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79625783-G-T

http://identifiers.org/hco/6/GRCh38#75205908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79625801-C-A

75205908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79625801-C-T

http://identifiers.org/hco/6/GRCh38#75205925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79625818-C-A

75205925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79625818-C-T

75205963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79625849-G-T

http://identifiers.org/hco/6/GRCh38#75205967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#79625853-C-A

75205967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2188
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79625853-C-T