Variant #0000926567 (NC_000017.10:g.56436044C>T, NM_017763.4:c.1093G>A (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.56436044C>T
DNA change (hg38) -
Published as RNF43(NM_017763.5):c.1093G>A (p.A365T), RNF43(NM_017763.6):c.1093G>A (p.A365T)
ISCN -
DB-ID RNF43_000024 See all 3 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) 0.00349 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
RNF43 NM_017763.4 -/. - c.1093G>A r.(?) p.(Ala365Thr)


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