Variant #0000721851 (NC_000008.10:g.145541990G>A, NM_005526.2:c.*3997G>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.145541990G>A
DNA change (hg38) -
Published as DGAT1(NM_012079.5):c.610C>T (p.L204F)
ISCN -
DB-ID DGAT1_000012
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) 5.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
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.*3997G>A r.(=) p.(=)
DGAT1 NM_012079.4 ?/. - c.610C>T r.(?) p.(Leu204Phe)


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