Variant #0000693756 (NC_000023.10:g.77369596T>C, NM_000291.3:c.356T>C (PGK1))

Chromosome X
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.77369596T>C
DNA change (hg38) -
Published as PGK1(NM_000291.3):c.356T>C (p.(Leu119Pro)), PGK1(NM_000291.4):c.356T>C (p.L119P)
ISCN -
DB-ID PGK1_000036 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) 0.00068 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGK1 NM_000291.3 -?/. - c.356T>C r.(?) p.(Leu119Pro)


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