Variant #0000534186 (NC_000008.10:g.145540277G>A, NM_005526.2:c.*2284G>A (HSF1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145540277G>A
DNA change (hg38) g.144316614G>A
Published as DGAT1(NM_012079.5):c.1407C>T (p.V469=), DGAT1(NM_012079.6):c.1407C>T (p.V469=)
ISCN -
DB-ID HSF1_000007 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) 0.00112 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF1 NM_005526.2 -?/. - c.*2284G>A r.(=) p.(=)
DGAT1 NM_012079.4 -?/. - c.1407C>T r.(?) p.(Val469=)


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