Variant #0000251083 (NC_000007.13:g.44104788A>C, NM_000290.3:c.341T>G (PGAM2))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44104788A>C
DNA change (hg38) g.44065189A>C
Published as PGAM2(NM_000290.3):c.341T>G (p.(Ile114Ser)), PGAM2(NM_000290.4):c.341T>G (p.I114S)
ISCN -
DB-ID PGAM2_000002 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) 0.0271 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.341T>G r.(?) p.(Ile114Ser)
DBNL NM_014063.6 -/. - c.*4273A>C r.(=) p.(=)


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