Variant #0000540024 (NC_000010.10:g.54031101T>G, NC_000010.10(NM_006258.3):c.1174-9T>G (PRKG1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54031101T>G
DNA change (hg38) g.52271341T>G
Published as PRKG1(NM_001098512.3):c.1129-9T>G
ISCN -
DB-ID PRKG1_000048
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) 8.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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.1174-9T>G r.(=) p.(=)
CSTF2T NM_015235.2 -?/. - c.-571792A>C r.(?) p.(=)


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