Variant #0001046728 (NC_000019.9:g.30193732C>T, NM_001256047.1:c.313G>A (C19orf12))

Chromosome 19
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.30193732C>T
DNA change (hg38) -
Published as C19orf12(NM_001031726.3):c.346G>A (p.V116M), C19orf12(NM_001031726.4):c.313G>A (p.V105M), C19orf12(NM_001282931.1):c.121G>A (p.V41M)
ISCN -
DB-ID C19orf12_000006 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) 0.00096 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 2025-07-08 13:22:38 +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     
C19orf12 NM_001256047.1 -?/. - c.313G>A r.(?) p.(Val105Met)


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