Variant #0000863927 (NC_000015.9:g.63982763C>T, NM_003922.3:c.5914G>A (HERC1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.63982763C>T
DNA change (hg38) -
Published as HERC1(NM_003922.3):c.5914G>A (p.V1972I), HERC1(NM_003922.4):c.5914G>A (p.(Val1972Ile))
ISCN -
DB-ID HERC1_000090 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00027 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HERC1 NM_003922.3 ?/. - c.5914G>A r.(?) p.(Val1972Ile)


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