161547096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42311714-A-G

161547097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42311713-G-A

161547097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42311713-G-T

161547100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42311710-G-C

161547100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42311710-G-T

161547203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311610-G-C

161547203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311610-G-T

161547277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311534-A-G

161547277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311534-A-T

161547321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42311488-G-T

161547731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42311064-T-A

161547739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42311058-A-G

http://identifiers.org/hco/5/GRCh38#161547784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#42311026-C-A

161547784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42311026-C-G

161547784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42311026-C-T

161547794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42311016-G-A

161547794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42311016-G-T

161547842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42310958-G-A

161547938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310810-C-G

161547938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310810-C-T

161547944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310804-G-A

161547944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310804-G-T

http://identifiers.org/hco/5/GRCh38#161548013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42310761-C-A

161548013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310761-C-G

161548013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310761-C-T

161548150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310639-T-C

http://identifiers.org/hco/5/GRCh38#161548188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42310610-C-A

161548188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310610-C-T

161548285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310547-G-T

http://identifiers.org/hco/5/GRCh38#161548306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42310526-C-A

161548306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310526-C-T

161548316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310516-T-C

http://identifiers.org/hco/5/GRCh38#161548335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42310496-C-A

161548335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310496-C-T

161548359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42310474-T-C

161548675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310206-G-A

161548839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42310049-G-A

161548895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42309998-G-T

161548958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42309942-G-A

http://identifiers.org/hco/5/GRCh38#161549005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42309897-C-A

http://identifiers.org/hco/5/GRCh38#161549047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#42309855-C-A

161549108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309773-G-A

161549108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309773-G-T

161549140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309744-G-A

161549140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309744-G-C

161549140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309744-G-T

161549185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309696-G-A

161549185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309696-G-T

161549307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309571-C-T

161549322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309556-C-G

161549349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309529-A-G

http://identifiers.org/hco/5/GRCh38#161549355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42309523-A-C

161549357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309521-G-A

161549718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42309187-G-A

161550123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42308919-A-G

161554198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42306228-G-T

161554271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42306152-A-T

161554387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42306045-A-T

161554642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305801-G-A

161554642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305801-G-T

161554665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305778-T-C

161554678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305764-C-G

161554817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305625-A-G

161554828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305611-T-A

161554828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42305611-T-C

161555787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304601-A-T

161556162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42304247-A-T

161556321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303983-C-T

161556374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303955-C-T

161556583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303731-A-T

161556779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303531-T-C

http://identifiers.org/hco/5/GRCh38#161556888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42303427-A-C

161557032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42303272-G-C

161557390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302584-T-G

161557441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302550-A-G

161557461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42302530-C-G

161559296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301627-G-A

161559296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301627-G-T

161559458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301484-A-G

161559511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301404-C-T

161559683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301240-G-A

161559683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301240-G-C

161559871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42301063-A-G

161560618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299856-T-C

161560749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299689-G-T

161560863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299627-G-A

161561363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299099-A-G

161561459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299017-G-A

161561459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42299017-G-T

http://identifiers.org/hco/5/GRCh38#161561491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42298990-C-A

161561491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298990-C-T

161561653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298824-T-A

161561653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298824-T-C

161561909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298593-C-G

http://identifiers.org/hco/5/GRCh38#161562278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42298288-A-C

161562278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298288-A-T

161562324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298265-T-C

161562337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42298252-T-C

http://identifiers.org/hco/5/GRCh38#161562441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42297684-C-A

161562441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42297684-C-G

http://identifiers.org/hco/5/GRCh38#161562804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42297266-A-C

161562856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42297220-G-A

161563165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296909-C-T

161563320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296751-G-C

161563351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296708-A-G

161563990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296091-C-G

161563991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296090-T-C

161563991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296090-T-G

161564059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42296024-A-G

161564133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42295947-G-A

161564239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42295848-A-G

161564284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42295807-T-G

http://identifiers.org/hco/5/GRCh38#161564302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42295789-C-A

161564326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42295761-A-G

161566133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42294675-A-G

http://identifiers.org/hco/5/GRCh38#161566153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42294657-A-C

http://identifiers.org/hco/5/GRCh38#161566204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42294598-A-C

161566204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42294598-A-G

161566261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42294544-T-C

161566313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42294493-C-T

161566455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42294359-T-C

161568754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42293495-C-T

161569047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42293190-T-A

161569047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42293190-T-C

161569429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292912-C-T

161569462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292909-A-G

161569477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292895-C-T

161569508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292864-T-C

161569517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292856-G-A

161569527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292845-T-C

http://identifiers.org/hco/5/GRCh38#161569711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42292670-C-A

161569711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292670-C-G

161569711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292670-C-T

161569784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292527-C-T

161569789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292522-T-A

161569797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292514-C-T

161569849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292466-C-T

161570002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292363-A-G

161570009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292356-A-G

161570009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292356-A-T

161570096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292279-G-A

161570759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292102-T-C

161570791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42292072-G-T

161570881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291990-C-T

161571079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291786-T-C

161571148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291740-C-T

161571451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291437-C-G

161571616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291271-A-G

http://identifiers.org/hco/5/GRCh38#161571640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42291246-C-A

161571640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291246-C-T

161571648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291238-G-C

161571648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42291238-G-T

http://identifiers.org/hco/5/GRCh38#161573120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42289752-C-A

161573237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288783-G-A

161573320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288703-G-A

http://identifiers.org/hco/5/GRCh38#161573486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42288586-A-C

161573593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288480-C-T

161573617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42288456-T-C

161577206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285168-C-T

http://identifiers.org/hco/5/GRCh38#161577283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42285076-A-C

161577332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42285033-A-G

http://identifiers.org/hco/5/GRCh38#161577776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42284473-C-A

http://identifiers.org/hco/5/GRCh38#161577795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42284454-C-A

161577795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284454-C-G

161577849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284400-G-A

161578139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42284028-A-G

161578440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283713-C-T

161578473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283679-G-T

161580065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42283028-G-A

161580390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282609-A-G

161580414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282585-G-A

161580570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282343-A-T

161580574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282339-T-C

161580621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42282209-A-G

161580852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281966-C-T

http://identifiers.org/hco/5/GRCh38#161580962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42281875-A-C

161581020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281825-T-A

161581020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281825-T-C

161581248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281595-T-C

161581724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42281081-G-A

161582877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279491-A-G

161583014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42279365-A-G

http://identifiers.org/hco/5/GRCh38#161584617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42277659-C-A

http://identifiers.org/hco/5/GRCh38#161585070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42277211-C-A

161585073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277208-T-C

161585148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277137-G-T

161585163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277120-T-C

161585276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42277008-T-C

http://identifiers.org/hco/5/GRCh38#161585332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42276979-C-A

161585339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276972-T-C

161585360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276951-A-G

http://identifiers.org/hco/5/GRCh38#161585427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42276886-A-C

161585514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276801-T-C

161585771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276557-G-A

161585800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276528-G-A

161586135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276183-T-C

161586285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42276035-C-T

http://identifiers.org/hco/5/GRCh38#161599390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42275249-C-A

161599668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42275000-G-A

161601594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273714-T-C

161601620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273688-G-A

161601769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273544-G-A

161602010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273310-T-C

161602051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273268-T-C

161602066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42273253-G-T

161602388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272919-T-A

161602388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272919-T-C

161602440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272866-G-A

http://identifiers.org/hco/5/GRCh38#161602616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42272702-A-C

161602719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42272605-A-G

161603156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42271202-G-A

161603303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42271053-T-G

http://identifiers.org/hco/5/GRCh38#161603417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42270938-A-C

161603441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42270914-A-G

161603473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42270882-T-C

http://identifiers.org/hco/5/GRCh38#161603486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42270871-C-A

161603486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42270871-C-T

161604612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42269897-T-A

161604878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42269624-T-C

161605091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42269390-T-G

161605097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42269383-A-G

161605425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42269088-G-A

161612590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42268494-C-T

http://identifiers.org/hco/5/GRCh38#161614045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42267235-C-A

161614131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42267158-C-T

161614215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42267089-A-G

161614298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42267008-T-G

161614322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42266981-A-G

http://identifiers.org/hco/5/GRCh38#161614353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42266950-A-C

161614542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42266692-T-C

161614751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42266514-C-T

http://identifiers.org/hco/5/GRCh38#161624301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42263169-A-C

161624638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262919-T-C

161624687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262867-T-A

161624788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262790-G-A

http://identifiers.org/hco/5/GRCh38#161624848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42262731-C-A

161625423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262249-A-G

161625641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42262038-T-C

161625705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261960-C-T

161625724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261933-G-T

161625808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261857-A-T

161626165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261535-A-G

http://identifiers.org/hco/5/GRCh38#161626319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42261372-A-C

161626397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42261286-T-C

161626807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260902-G-A

161626847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260861-A-G

161626919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260812-T-C

161627080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260658-G-A

161627288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42260051-A-G

161627465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259846-A-G

161627508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259795-A-G

161627574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259749-A-G

161627995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259137-A-T

161628098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42259044-C-G

161630056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258697-C-T

161636181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42258417-T-C

161636600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42257668-A-G

http://identifiers.org/hco/5/GRCh38#161636653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42257614-C-A

161636879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: non coding transcript exon variant
orthologous variants: 42257372-G-C

161636922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42257329-A-G

161637075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42257185-G-A

http://identifiers.org/hco/5/GRCh38#161637247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42257028-C-A

161637435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256890-G-T

161637800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256539-C-T

161637808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256531-A-T

161637858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256481-T-A

161637927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256417-T-C

161637947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256398-G-A

161638039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42256291-A-G

161638167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255954-G-A

161638167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255954-G-T

161638265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255851-A-G

161638377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42255739-T-G

161639442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254043-T-G

161639482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42254003-G-A

161639900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42252753-A-G

161642780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42247899-A-G

161642843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245766-G-A

161642881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245728-C-T

161642912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245700-G-A

161643019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245589-T-G

161643031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42245576-A-G

161665502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222524-C-T

161665547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222479-G-A

161665688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222333-T-C

161665729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222296-C-T

161665733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222292-A-G

http://identifiers.org/hco/5/GRCh38#161665775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42222246-A-C

161665937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222109-A-G

161668402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42222037-G-A

161668944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42221613-A-G

161669194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220938-G-A

161669232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220900-C-T

161669338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220808-G-T

161669401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220745-A-G

161669603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220530-A-G

161669809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220327-A-T

161669907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42220225-G-C

http://identifiers.org/hco/5/GRCh38#161670266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42219297-A-C

161671359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42218969-C-T

161676228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42217502-C-T

161676590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42217154-C-T

161676627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42217122-A-T

161676695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42217055-T-C

161676794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216957-G-T

http://identifiers.org/hco/5/GRCh38#161676910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42216830-C-A

161676989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216747-G-A

161676989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216747-G-T

161677034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216704-G-A

161677120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42216621-G-T

161677742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215909-T-G

http://identifiers.org/hco/5/GRCh38#161677761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42215871-A-C

161677783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215852-A-G

161677788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215847-A-T

161677946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215700-C-T

161678237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215427-G-T

161678286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215337-G-C

161678353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215280-T-G

161678566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215078-A-T

161678619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42215024-G-A

161678646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42214997-G-C

http://identifiers.org/hco/5/GRCh38#161681070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42213965-C-A

161681312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213750-G-A

161682147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42213039-C-G

161682335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212817-G-A

161682442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212708-G-A

161682723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212481-C-T

161682774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212435-T-C

161685438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212107-G-T

161685450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42212095-G-T

http://identifiers.org/hco/5/GRCh38#161685591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42211961-C-A

161685591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211961-C-T

http://identifiers.org/hco/5/GRCh38#161685639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42211913-C-A

161685639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211913-C-T

161685716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42211865-G-A

161685716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42211865-G-T

http://identifiers.org/hco/5/GRCh38#161685771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42211810-C-A

161685797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42211781-G-T

161685850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42211730-T-C

http://identifiers.org/hco/5/GRCh38#161686126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42211431-C-A

161686167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42211390-G-A

161686250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42211307-A-G

161686250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42211307-A-T

161686387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211165-T-C

161686390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211162-C-G

161686390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211162-C-T

161686392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211160-T-C

161686392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211160-T-G

161686398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211154-G-A

161686398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211154-G-C

161686398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211154-G-T

161686411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211141-G-T

161686449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211095-G-T

161686461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211086-G-C

161686461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211086-G-T

161686475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211070-G-A

161686475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211070-G-T

http://identifiers.org/hco/5/GRCh38#161686488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42211057-C-A

161686488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211057-C-T

http://identifiers.org/hco/5/GRCh38#161686489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42211056-A-C

161686489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42211056-A-T

http://identifiers.org/hco/5/GRCh38#161686794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42210694-C-A

161686794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210694-C-G

161686797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210691-G-C

http://identifiers.org/hco/5/GRCh38#161686896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42210600-C-A

161687013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210483-T-A

161687013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210483-T-C

161687049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210461-G-C

161687049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210461-G-T

161687069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210441-T-C

161687138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210387-G-A

161687138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42210387-G-T

http://identifiers.org/hco/5/GRCh38#161687570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42210044-C-A

http://identifiers.org/hco/5/GRCh38#161687647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42209966-C-A

161687647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 42209966-C-G

161687832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209755-A-G

161688253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209373-A-G

http://identifiers.org/hco/5/GRCh38#161688322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42209307-A-C

161688322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209307-A-T

161688409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209219-C-T

161688565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42209068-G-A

161688677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208947-T-C

161688846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42208700-T-C

161689161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42208391-C-T

161689424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron variant
orthologous variants: 42208140-A-G

161689446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron variant
orthologous variants: 42208118-G-A

http://identifiers.org/hco/5/GRCh38#161689475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42208096-C-A

161689475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron variant
orthologous variants: 42208096-C-T

http://identifiers.org/hco/5/GRCh38#161689600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42207974-A-C

161689600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42207974-A-G

161689788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42207781-T-C

161689829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42207751-G-A

http://identifiers.org/hco/5/GRCh38#161689966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42207629-A-C

161690016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42207583-A-G

161690062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42207546-T-G

161690140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42207463-A-G

161690344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42207264-A-T

161690373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207235-C-T

161690464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207137-G-A

161690464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207137-G-C

http://identifiers.org/hco/5/GRCh38#161690502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42207108-C-A

161690502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207108-C-T

161690542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42207065-A-T

161690775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206848-T-C

http://identifiers.org/hco/5/GRCh38#161690992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42206647-A-C

http://identifiers.org/hco/5/GRCh38#161691072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42206592-C-A

http://identifiers.org/hco/5/GRCh38#161691748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42206178-C-A

161691862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206101-T-C

161691868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206095-G-T

161691869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206094-A-T

161691926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206041-T-A

161691926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206041-T-C

161691926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206041-T-G

161691931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42206036-T-C

161692168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42205799-G-A

161692168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42205799-G-C

161692181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42205786-T-C

161692186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42205781-G-C

161692250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205716-A-T

161692264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205702-A-G

161692293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205674-G-A

161692293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205674-G-T

161692303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205664-G-A

161692303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205664-G-T

161692390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205583-T-A

161692656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42205311-G-A

http://identifiers.org/hco/5/GRCh38#161692675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42205293-C-A

161694085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42204834-A-G

161694521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42204233-G-A

161694870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203904-C-G

161694870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203904-C-T

161694871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203903-G-A

161694871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203903-G-C

161694909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203865-G-A

161696076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42203206-A-G

161696554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42202813-G-T

161696703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42202689-G-A

161697417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201718-T-C

161697485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201646-C-G

161697590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201531-T-A

161697777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201352-C-G

161697797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201332-C-T

161697801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42201328-C-T

161699224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200933-G-A

161699267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200893-A-G

161699415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200737-T-A

161699415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200737-T-G

161699417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200735-T-C

161699647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200572-A-G

161699893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200437-G-A

161700139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42200194-C-T

161700488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199845-A-T

161700573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199761-T-C

161700573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199761-T-G

161700580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199754-T-C

http://identifiers.org/hco/5/GRCh38#161700775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42199561-A-C

161700814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42199528-A-G

http://identifiers.org/hco/5/GRCh38#161701442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42198419-C-A

161701442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42198419-C-G

161701542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42198316-G-C

http://identifiers.org/hco/5/GRCh38#161702086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#42197744-A-C

161702563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4080
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42197293-A-T