Variant #0001065779 (NC_000012.11:g.64712543T>C, NC_000012.11(NM_001099676.2):c.488+12197A>G (C12orf56))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.64712543T>C
DNA change (hg38) -
Published as C12orf56(NM_001170633.2):c.706A>G (p.(Ile236Val))
ISCN -
DB-ID C12orf56_000004
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) 0.00025 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf56 NM_001099676.2 ?/. - c.488+12197A>G r.(=) p.(=)


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