Variant #0001054300 (NC_000012.11:g.48536638A>T, NM_000289.5:c.1727A>T (PFKM))

Chromosome 12
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.48536638A>T
DNA change (hg38) -
Published as PFKM(NM_000289.6):c.1727A>T (p.(Tyr576Phe))
ISCN -
DB-ID ASB8_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) 0.00018 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
PFKM NM_000289.5 ?/. - c.1727A>T r.(?) p.(Tyr576Phe)
PFKM NM_001166686.1 ?/. - c.1940A>T r.(?) p.(Tyr647Phe)
SENP1 NM_001267594.1 ?/. - c.-36872T>A r.(?) p.(=)
ASB8 NM_024095.3 ?/. - c.*6511T>A r.(=) p.(=)


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