Variant #0000808658 (NC_000019.9:g.11541831C>T, NM_001001329.1:c.-4774C>T (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.11541831C>T
DNA change (hg38) -
Published as CCDC151(NM_001302453.1):c.92G>A (p.(Arg31Gln)), CCDC151(NM_145045.4):c.254G>A (p.R85Q)
ISCN -
DB-ID CCDC151_000011 See all 3 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) 0.00367 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +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.-4774C>T r.(?) p.(=)
CCDC151 NM_145045.4 -?/. - c.254G>A r.(?) p.(Arg85Gln)


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