Variant #0000912757 (NC_000007.13:g.44104896C>T, NM_000290.3:c.233G>A (PGAM2))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44104896C>T
DNA change (hg38) -
Published as PGAM2(NM_000290.4):c.233G>A (p.W78*)
ISCN -
DB-ID DBNL_000011
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) 0.00051 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGAM2 NM_000290.3 +/. - c.233G>A r.(?) p.(Trp78*)
DBNL NM_014063.6 +/. - c.*4381C>T r.(=) p.(=)


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