Variant #0000889155 (NC_000010.10:g.54011419T>C, NM_006258.3:c.1166T>C (PRKG1))

Chromosome 10
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.54011419T>C
DNA change (hg38) -
Published as PRKG1(NM_001098512.3):c.1121T>C (p.V374A), PRKG1(NM_006258.4):c.1166T>C (p.V389A)
ISCN -
DB-ID CSTF2T_000004 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 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKG1 NM_006258.3 ?/. - c.1166T>C r.(?) p.(Val389Ala)
CSTF2T NM_015235.2 ?/. - c.-552110A>G r.(?) p.(=)


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