http://identifiers.org/hco/1/GRCh38#179741989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156033927-A-C

179742459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156033516-G-A

179742616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156033382-C-T

179742627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156033370-G-A

179742631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156033366-G-T

179742843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156033064-G-T

179743019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032921-A-G

179743024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032916-G-A

179743024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032916-G-T

179743055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032885-G-A

179743103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032835-T-C

179743114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032821-G-A

179743189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032758-G-A

http://identifiers.org/hco/1/GRCh38#179743335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#156032622-C-A

179743335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 156032622-C-T

http://identifiers.org/hco/1/GRCh38#179743414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156032535-C-A

http://identifiers.org/hco/1/GRCh38#179743428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156032521-C-A

179743428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156032521-C-T

http://identifiers.org/hco/1/GRCh38#179743460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156032491-C-A

179743460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156032491-C-T

179743810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032264-C-G

179743833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156032241-C-G

179744148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156031917-G-A

179744583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156031483-A-T

http://identifiers.org/hco/1/GRCh38#179744705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156031346-C-A

179745094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156030941-A-T

179745383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156030516-G-A

179745645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156030255-A-G

http://identifiers.org/hco/1/GRCh38#179745737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156030155-C-A

179745737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156030155-C-G

179745737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156030155-C-T

179746115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156029781-G-A

179746757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156028897-C-T

179746774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156028884-T-C

http://identifiers.org/hco/1/GRCh38#179746791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156028867-C-A

179746945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156028740-T-G

179747058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156028636-G-C

179747134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156028576-T-G

179747164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156028546-T-A

http://identifiers.org/hco/1/GRCh38#179747312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156027842-C-A

179747312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027842-C-G

179747357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027799-C-T

179747377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027780-G-A

179747396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027761-G-A

179747597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027595-G-A

179747633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027566-C-T

179747650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027550-C-T

179747699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027502-C-T

179747700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027501-G-A

179747700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027501-G-T

179747858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027350-G-T

179747904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027308-G-A

179748026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027240-G-A

179748026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027240-G-T

179748236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156027069-G-C

179748544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156026782-C-T

179748572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156026754-G-A

179748588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156026738-C-T

179748755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156026600-G-A

179748770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156026585-T-G

179749189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025919-A-G

http://identifiers.org/hco/1/GRCh38#179749239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156025866-A-C

179749239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025866-A-T

179749406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025695-C-G

179750055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025353-C-T

179750082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025331-T-C

179750102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025312-A-G

179750198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025217-A-G

179750334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156025090-T-A

179753711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156021218-T-C

179753785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156021168-G-A

179753785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156021168-G-T

179754031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020924-A-T

179754071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020884-C-T

179754260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020592-G-A

http://identifiers.org/hco/1/GRCh38#179754300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156020552-A-C

179754389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020458-C-T

179754461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156020386-C-G

179754474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020373-A-G

179754679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020180-T-C

179754742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156020117-G-A

179755196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019962-A-G

179755290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019899-G-A

179755318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019870-T-C

179755429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019760-A-G

179755559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019648-A-G

179755583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019636-G-A

179755825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019293-A-T

179755865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019254-C-T

179755882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019237-C-T

179755921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019198-A-T

179756108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156019035-G-C

179757947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156018165-A-G

179758196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156017947-G-A

179758409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156017741-T-C

179759004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016395-C-G

179759089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016324-G-C

179759091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016322-G-A

179759104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016315-A-G

179759108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016311-T-G

179759128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016297-G-T

179759244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016200-G-A

179759364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016092-C-T

179759464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156016030-A-G

179760967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156013598-C-T

179761856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156011575-G-A

179761857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156011574-C-T

179762003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156011433-C-T

179762035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156011400-G-A

179762436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156010989-C-T

179762920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156010499-A-G

179762923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156010496-G-A

179762958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156010472-G-A

179763060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156010310-G-A

179763064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156010306-T-C

179763368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156009574-G-A

179763369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156009573-G-A

http://identifiers.org/hco/1/GRCh38#179763441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156009495-C-A

179763441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156009495-C-G

http://identifiers.org/hco/1/GRCh38#179763594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156009363-C-A

179763673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156009328-T-C

179763893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156009112-G-A

179764021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156008916-G-A

http://identifiers.org/hco/1/GRCh38#179764080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156008853-C-A

179765787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156008189-G-A

179767088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007882-C-T

179767103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007867-T-A

http://identifiers.org/hco/1/GRCh38#179767255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156007725-C-A

179767381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007601-C-T

179767426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007556-G-C

179767483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007493-T-A

179767647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007319-G-A

179767788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007132-G-A

179767788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007132-G-C

179767816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156007104-G-C

http://identifiers.org/hco/1/GRCh38#179768184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156003542-C-A

179768200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156003526-A-G

179768576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156003218-G-A

179770816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156001550-A-G

179770876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156001485-T-C

179770876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156001485-T-G

179771193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156001221-A-G

179771263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156001159-C-T

http://identifiers.org/hco/1/GRCh38#179771281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156001141-C-A

http://identifiers.org/hco/1/GRCh38#179771288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156001134-C-A

http://identifiers.org/hco/1/GRCh38#179771364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156001063-C-A

179771387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156001039-T-C

179771580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156000436-T-G

179771921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155999081-C-T

179772282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155998762-C-T

179772290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155998757-C-T

179772623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155998407-T-C

179772869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155998154-C-T

179772906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155998117-A-G

179773197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155997822-G-T

179773257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155997661-T-C

179773377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155997564-A-T

179773721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155997397-G-T

179773919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155997305-G-A

179774061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155997167-C-T

179776586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155994444-G-A

179776623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155994401-C-T

179777302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993861-T-C

179777425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993689-G-A

179777445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993669-G-A

179777461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993653-G-A

179777461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993653-G-C

179777465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993649-T-A

179777522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155993601-G-T

179778533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155990801-G-A

179778535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155990799-A-G

179778768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155990548-G-A

179778811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155990527-C-T

179779090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155990264-T-A

179779621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155989884-G-T

179779676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155989835-G-A

179779686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155989828-G-C

179779686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155989828-G-T

179779825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155989677-C-T

179780101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155989347-T-A

http://identifiers.org/hco/1/GRCh38#179780401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155989062-C-A

179780478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988873-C-T

http://identifiers.org/hco/1/GRCh38#179780604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155988732-C-A

179780604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988732-C-T

179780664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988686-C-T

179780971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988370-G-A

179781002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988339-A-G

179781011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988330-C-T

179781083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988278-G-A

179781105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988255-C-G

179781105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988255-C-T

179781174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988193-T-C

179781401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155988123-T-A

http://identifiers.org/hco/1/GRCh38#179782121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155987724-C-A

179782328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155987520-C-T

179782568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155987319-A-G

179782649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155987241-C-T

179782985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155986929-C-G

179784904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155984765-G-A

179785267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155984412-A-G

179785412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155984272-G-C

179785471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155984213-T-A

179786778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155982684-T-C

http://identifiers.org/hco/1/GRCh38#179787202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155982341-A-C

179787630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155981682-C-T

http://identifiers.org/hco/1/GRCh38#179787631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155981681-C-A

179787631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155981681-C-T

179787728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155981585-G-C

179788379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155980929-T-C

179788400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155980908-C-T

179788454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155980870-G-C

179790571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155979722-A-G

179791360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155978774-G-A

179791372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155978762-G-A

179791439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155978686-G-A

http://identifiers.org/hco/1/GRCh38#179793488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155974413-A-C

179793500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155974398-G-A

179794332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155973660-A-G

179794332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155973660-A-T

179795837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155971017-C-T

179795924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155970880-C-T

179796057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155970759-A-G

179796719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155969159-A-G

179803047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155966182-T-C

179803372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965849-T-C

179803433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965801-G-A

179803461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965771-G-C

179804038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965640-G-T

179804063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965615-G-T

http://identifiers.org/hco/1/GRCh38#179804114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155965547-C-A

179804114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965547-C-T

179804121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965540-G-T

http://identifiers.org/hco/1/GRCh38#179804149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155965511-C-A

179804149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965511-C-T

179804151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965509-A-G

179804153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155965499-A-G

179805923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964703-G-A

179806108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964525-G-C

http://identifiers.org/hco/1/GRCh38#179806282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155964357-A-C

179806282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964357-A-G

179806290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964335-A-G

179806294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964332-T-A

179806296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964330-A-T

179806303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155964284-G-T

179806579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155963949-G-T

179806598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155963933-G-A

179808027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155963393-T-C

179808030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155963390-G-T

179808148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155963273-G-A

179808265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155963149-T-C

179808671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155962680-G-A

179809880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155961880-C-T

179809951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155961801-G-C

179810077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155961665-C-T

179811429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155958249-G-A

179811909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155957224-G-A

http://identifiers.org/hco/1/GRCh38#179812092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155957175-C-A

179812153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155957114-T-C

179812268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155957011-C-T

http://identifiers.org/hco/1/GRCh38#179812276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155957003-C-A

http://identifiers.org/hco/1/GRCh38#179812446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155956876-A-C

179812573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155956826-G-A

179812573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155956826-G-C

http://identifiers.org/hco/1/GRCh38#179812738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155956647-C-A

179812779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155956620-C-T

179812803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155956597-T-A

179812803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155956597-T-C

179813035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155955852-G-A

179813035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155955852-G-T

179813104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155955782-G-T

http://identifiers.org/hco/1/GRCh38#179813199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155955687-C-A

179813199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955687-C-T

179813224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955662-A-G

179813225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955661-G-A

179813226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955660-G-A

http://identifiers.org/hco/1/GRCh38#179813272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155955603-C-A

http://identifiers.org/hco/1/GRCh38#179813371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155955504-C-A

179813535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955334-G-T

179813554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955300-A-T

179813609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955262-C-T

http://identifiers.org/hco/1/GRCh38#179813679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155955166-C-A

179813679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955166-C-G

179813679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955166-C-T

179813680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955165-T-C

179813729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955113-G-A

179813759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: intron variant
orthologous variants: 155955081-C-T

179813833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954997-G-C

179813848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954979-A-G

179813863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954964-C-T

179813888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954939-A-G

179813896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954931-G-T

179813906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954921-G-A

179814011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954819-C-T

179814033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: synonymous variant
orthologous variants: 155954797-G-C

179814033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: synonymous variant
orthologous variants: 155954797-G-T

179814055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: missense variant
orthologous variants: 155954775-T-C

179814082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: stop gained
orthologous variants: 155954748-G-T

http://identifiers.org/hco/1/GRCh38#179814201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155954630-C-A

179814225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3 prime UTR variant
orthologous variants: 155954607-G-A

179814259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3 prime UTR variant
orthologous variants: 155954572-A-G

http://identifiers.org/hco/1/GRCh38#179814314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155954520-C-A

179814314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954520-C-T

179814374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954462-G-A

179814374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954462-G-T

179814466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954375-G-T

http://identifiers.org/hco/1/GRCh38#179814477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155954365-A-C

179814496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954346-A-G

179814496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954346-A-T

179814559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954287-G-A

179814559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155954287-G-T

179814611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155954235-G-T

179814631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155954225-G-A

179814631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155954225-G-C

http://identifiers.org/hco/1/GRCh38#179814674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155954180-A-C

http://identifiers.org/hco/1/GRCh38#179814699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155954156-C-A

179814699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155954156-C-T

179814785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155954094-G-A

179814785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155954094-G-T

http://identifiers.org/hco/1/GRCh38#179814801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155954078-A-C

179814902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953964-G-T

http://identifiers.org/hco/1/GRCh38#179814907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155953959-C-A

179814907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953959-C-G

179814942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953936-C-T

179815008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953868-A-G

179815053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953827-G-A

179815053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953827-G-T

179815071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953809-G-A

179815071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953809-G-T

179815186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953731-T-C

179815251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953666-C-T

179815267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155953650-T-C

179815415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953513-G-T

179815422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953506-A-G

179815455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953475-T-A

179815490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953422-A-G

179815641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953214-T-C

179815706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953146-G-A

http://identifiers.org/hco/1/GRCh38#179815709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155953143-A-C

179815709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953143-A-G

179815794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953084-G-A

179815794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953084-G-T

179815815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953063-G-A

179815815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953063-G-T

179815901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953026-G-A

179815901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155953026-G-T

http://identifiers.org/hco/1/GRCh38#179815959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155952966-C-A

179815995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155952925-A-G

179815998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155952922-C-T

http://identifiers.org/hco/1/GRCh38#179816080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155952864-C-A

179816080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155952864-C-T

179816104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155952840-G-T

179816158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28274
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155952786-G-A