Variant #0000534180 (NC_000008.10:g.145535873_145535874dup, NM_005526.2:c.1085_1086dup (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.145535873_145535874dup
DNA change (hg38) g.144312187_144312188dup
Published as HSF1(NM_005526.2):c.1083_1084insCC (p.(Ser363ProfsTer15))
ISCN -
DB-ID HSF1_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF1 NM_005526.2 -?/. - c.1085_1086dup r.(?) p.(Ser363ProfsTer15)
DGAT1 NM_012079.4 -?/. - c.*4344_*4345dup r.(=) p.(=)


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