Variant #0000566796 (NC_000019.9:g.30193654T>C, NM_001256047.1:c.391A>G (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.30193654T>C
DNA change (hg38) g.29702747T>C
Published as C19orf12(NM_001031726.3):c.424A>G (p.K142E), C19orf12(NM_001282931.2):c.199A>G (p.K67E), C19orf12(NM_001282931.3):c.199A>G (p.K67E), C19orf12(NM_0...)
ISCN -
DB-ID C19orf12_000013 See all 4 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) 0.00229 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.391A>G r.(?) p.(Lys131Glu)


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