Variant #0000655831 (NC_000007.13:g.44104494del, NM_000290.3:c.533del (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.44104494del
DNA change (hg38) g.44064895del
Published as PGAM2(NM_000290.3):c.533delG (p.G178Afs*31)
ISCN -
DB-ID DBNL_000004
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-22 15:46:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGAM2 NM_000290.3 +/. - c.533del r.(?) p.(Gly178AlafsTer31)
DBNL NM_014063.6 +/. - c.*3979del r.(?) p.(=)


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