Variant #0000606367 (NC_000002.11:g.179315141_179315142insAAGGTCC, NC_000002.11(NM_003690.4):c.66-4_66-3insGGACCTT (PRKRA))

Chromosome 2
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.179315141_179315142insAAGGTCC
DNA change (hg38) -
Published as PRKRA(NM_001139517.1):c.29_30insGGACCTT (p.C10Wfs*12), PRKRA(NM_001139517.1):c.30_31insCGTCCCTTCTCGCCCTGTCCCAGAGCAGGCACCGCCGAGGCCCCGCCGCTGGAGCGCGAG...
ISCN -
DB-ID DFNB59_000012 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNB59 NM_001042702.3 -?/. - c.-1378_-1377insAAGGTCC r.(?) p.(=)
PRKRA NM_003690.4 -?/. - c.66-4_66-3insGGACCTT r.spl? p.?


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