Variant #0000864877 (NC_000016.9:g.67201734G>T, NM_001374675.1:c.966G>T (HSF4))

Chromosome 16
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.67201734G>T
DNA change (hg38) -
Published as HSF4(NM_001040667.2):c.966G>T (p.P322=)
ISCN -
DB-ID FBXL8_000016
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_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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0895L NM_001040715.1 -?/. - c.*8980C>A r.(=) p.(=)
HSF4 NM_001374675.1 -?/. - c.966G>T r.(?) p.(Pro322=)
FBXL8 NM_018378.2 -?/. - c.*4011G>T r.(=) p.(=)


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