Variant #0000804447 (NC_000010.10:g.53921640G>A, NC_000010.10(NM_006258.3):c.1002-9G>A (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.53921640G>A
DNA change (hg38) -
Published as PRKG1(NM_001098512.3):c.957-9G>A, PRKG1(NM_006258.4):c.1002-9G>A
ISCN -
DB-ID PRKG1_000020 See all 3 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) 0.00022 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 2021-09-17 14:40:49 +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.1002-9G>A r.(=) p.(=)
CSTF2T NM_015235.2 -?/. - c.-462331C>T r.(?) p.(=)


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