Variant #0000851838 (NC_000008.10:g.145541761G>A, NM_005526.2:c.*3768G>A (HSF1))

Chromosome 8
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.145541761G>A
DNA change (hg38) -
Published as DGAT1(NM_012079.5):c.748C>T (p.R250C)
ISCN -
DB-ID DGAT1_000017
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) 0.00017 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 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF1 NM_005526.2 ?/. - c.*3768G>A r.(=) p.(=)
DGAT1 NM_012079.4 ?/. - c.748C>T r.(?) p.(Arg250Cys)


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