Variant #0000894761 (NC_000019.9:g.11533433_11533435del, NM_001001329.1:c.-13172_-13170del (PRKCSH))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11533433_11533435del
DNA change (hg38) -
Published as ODAD3(NM_145045.5):c.1213_1215delGAG (p.E405del)
ISCN -
DB-ID CCDC151_000015
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.-13172_-13170del r.(?) p.(=)
RGL3 NM_001035223.2 ?/. - c.-3479_-3477del r.(?) p.(=)
CCDC151 NM_145045.4 ?/. - c.1213_1215del r.(?) p.(Glu405del)


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