Variant #0001042867 (NC_000019.9:g.36034590G>A, NM_032635.3:c.-2052G>A (TMEM147))

Chromosome 19
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.36034590G>A
DNA change (hg38) -
Published as GAPDHS(NM_014364.5):c.917G>A (p.(Arg306Gln))
ISCN -
DB-ID GAPDHS_000001
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
GAPDHS NM_014364.4 ?/. - c.917G>A r.(?) p.(Arg306Gln)
TMEM147 NM_032635.3 ?/. - c.-2052G>A r.(?) p.(=)


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