Variant #0000566017 (NC_000019.9:g.11557167T>C, NC_000019.9(NM_001001329.1):c.762+2T>C (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.11557167T>C
DNA change (hg38) g.11446352T>C
Published as -
ISCN -
DB-ID ELAVL3_000003
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 12:26:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKCSH NM_001001329.1 +/. - c.762+2T>C r.spl? p.?
ELAVL3 NM_001420.3 +/. - c.*8174A>G r.(=) p.(=)


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