Variant #0000681355 (NC_000019.9:g.30196302C>T, NC_000019.9(NM_001256047.1):c.161-2418G>A (C19orf12))

Chromosome 19
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.30196302C>T
DNA change (hg38) -
Published as C19orf12(NM_001282931.1):c.-153-1G>A, C19orf12(NM_001282931.3):c.-153-1G>A
ISCN -
DB-ID C19orf12_000024 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C19orf12 NM_001256047.1 ?/. - c.161-2418G>A r.(=) p.(=)


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