Variant #0000690010 (NC_000007.13:g.44105095C>T, NM_000290.3:c.34G>A (PGAM2))

Chromosome 7
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.44105095C>T
DNA change (hg38) -
Published as PGAM2(NM_000290.3):c.34G>A (p.G12S)
ISCN -
DB-ID DBNL_000008
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
PGAM2 NM_000290.3 ?/. - c.34G>A r.(?) p.(Gly12Ser)
DBNL NM_014063.6 ?/. - c.*4580C>T r.(=) p.(=)


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