Variant #0000562431 (NC_000017.10:g.56492800T>C, NM_017763.4:c.139A>G (RNF43))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56492800T>C
DNA change (hg38) g.58415439T>C
Published as RNF43(NM_017763.6):c.139A>G (p.I47V)
ISCN -
DB-ID HSF5_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) 0.41182 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF5 NM_001080439.1 -/. - c.*6921A>G r.(=) p.(=)
RNF43 NM_017763.4 -/. - c.139A>G r.(?) p.(Ile47Val)


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