Variant #0000566022 (NC_000019.9:g.11558370_11558372dup, NM_001001329.1:c.966_968dup (PRKCSH))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11558370_11558372dup
DNA change (hg38) g.11447555_11447557dup
Published as PRKCSH(NM_001289103.1):c.966_968dupGGA (p.E325dup), PRKCSH(NM_002743.3):c.966_968dupGGA (p.E325dup)
ISCN -
DB-ID ELAVL3_000005 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKCSH NM_001001329.1 -/. - c.966_968dup r.(?) p.(Glu325dup)
ELAVL3 NM_001420.3 -/. - c.*6998_*7000dup r.(=) p.(=)


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