Variant #0000510334 (NC_000002.11:g.179312316_179312317insTGC, NC_000002.11(NM_003690.4):c.236-4_236-3insGCA (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.179312316_179312317insTGC
DNA change (hg38) g.178447589_178447590insTGC
Published as PRKRA(NM_001139517.1):c.203-4_203-3insGCA
ISCN -
DB-ID DFNB59_000004
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-09 19:35:13 +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.-4203_-4202insTGC r.(?) p.(=)
PRKRA NM_003690.4 -/. - c.236-4_236-3insGCA r.spl? p.?


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