Variant #0000894764 (NC_000019.9:g.11547014_11547021dup, NC_000019.9(NM_001001329.1):c.76_79+4dup (PRKCSH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.11547014_11547021dup
DNA change (hg38) -
Published as PRKCSH(NM_002743.3):c.79_80insGTGAACCA (p.N27Sfs*117)
ISCN -
DB-ID CCDC151_000018
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.76_79+4dup r.spl? p.?
CCDC151 NM_145045.4 +/. - c.-1184_-1177dup r.(?) p.(=)


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