Variant #0000297140 (NC_000016.9:g.8904945C>A, NM_000303.2:c.357C>A (PMM2))

Chromosome 16
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.8904945C>A
DNA change (hg38) g.8811088C>A
Published as PMM2(NM_000303.2):c.357C>A (p.F119L, p.(Phe119Leu)), PMM2(NM_000303.3):c.357C>A (p.F119L)
ISCN -
DB-ID PMM2_000007 See all 28 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMM2 NM_000303.2 +/. - c.357C>A r.(?) p.(Phe119Leu)


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