Variant #0000928323 (NC_000002.11:g.179312283T>C, NM_003690.4:c.266A>G (PRKRA))

Chromosome 2
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.179312283T>C
DNA change (hg38) -
Published as PRKRA(NM_003690.5):c.266A>G (p.H89R)
ISCN -
DB-ID DFNB59_000057
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNB59 NM_001042702.3 ?/. - c.-4236T>C r.(?) p.(=)
PRKRA NM_003690.4 ?/. - c.266A>G r.(?) p.(His89Arg)


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