Variant #0000951202 (NC_000019.9:g.11533276C>A, NM_001001329.1:c.-13329C>A (PRKCSH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.11533276C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CCDC151_000019
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-11-27 17:35:39 +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.-13329C>A r.(?) p.(=)
RGL3 NM_001035223.2 +?/. - c.-3322G>T r.(?) p.(=)
CCDC151 NM_145045.4 +?/. - c.1297G>T r.(?) p.(Glu433*)


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