Variant #0000998322 (NC_000010.10:g.54011333T>C, NM_006258.3:c.1080T>C (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.54011333T>C
DNA change (hg38) -
Published as PRKG1(NM_001098512.3):c.1035T>C (p.Y345=), PRKG1(NM_006258.4):c.1080T>C (p.Y360=)
ISCN -
DB-ID PRKG1_000024 See all 2 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) 0.00136 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 2024-08-28 13:16:32 +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     
PRKG1 NM_006258.3 -/. - c.1080T>C r.(?) p.(Tyr360=)
CSTF2T NM_015235.2 -/. - c.-552024A>G r.(?) p.(=)


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