Variant #0000297363 (NC_000002.11:g.179315738_179315739del, NM_003690.4:c.22_23del (PRKRA))

Chromosome 2
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.179315738_179315739del
DNA change (hg38) g.178451011_178451012del
Published as PRKRA(NM_003690.5):c.22_23delGC (p.A8Rfs*22)
ISCN -
DB-ID PRKRA_000028
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNB59 NM_001042702.3 -/. - c.-781_-780del r.(?) p.(=)
PRKRA NM_003690.4 -/. - c.22_23del r.(?) p.(Ala8ArgfsTer22)


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