Variant #0001046729 (NC_000019.9:g.30199335G>A, NC_000019.9(NM_001256047.1):c.-10-5C>T (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.30199335G>A
DNA change (hg38) -
Published as C19orf12(NM_001031726.3):c.24-5C>T, C19orf12(NM_001282931.1):c.-323-5C>T, C19orf12(NM_001282931.3):c.-323-5C>T
ISCN -
DB-ID C19orf12_000019 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) 0.00015 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.-10-5C>T r.spl? p.?


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