Variant #0000299100 (NC_000010.10:g.52913020G>A, NM_006258.3:c.408G>A (PRKG1))

Chromosome 10
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.52913020G>A
DNA change (hg38) g.51153260G>A
Published as PRKG1(NM_001098512.3):c.363G>A (p.P121=)
ISCN -
DB-ID PRKG1_000011
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) 0.01732 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKG1 NM_006258.3 -/. - c.408G>A r.(?) p.(Pro136=)
CSTF2T NM_015235.2 -/. - c.*544439C>T r.(=) p.(=)


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