Variant #0000692675 (NC_000019.9:g.11557949G>A, NM_001001329.1:c.823G>A (PRKCSH))

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.11557949G>A
DNA change (hg38) -
Published as PRKCSH(NM_001289103.1):c.823G>A (p.A275T)
ISCN -
DB-ID ELAVL3_000010
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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
PRKCSH NM_001001329.1 -?/. - c.823G>A r.(?) p.(Ala275Thr)
ELAVL3 NM_001420.3 -?/. - c.*7392C>T r.(=) p.(=)


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