Variant #0001065728 (NC_000012.11:g.48528601C>T, NM_000289.5:c.736C>T (PFKM))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48528601C>T
DNA change (hg38) -
Published as PFKM(NM_000289.6):c.736C>T (p.(Arg246*))
ISCN -
DB-ID PFKM_000021
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 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 2026-01-20 18:57:21 +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.736C>T r.(?) p.(Arg246*)
PFKM NM_001166686.1 +?/. - c.949C>T r.(?) p.(Arg317*)
SENP1 NM_001267594.1 +?/. - c.-28835G>A r.(?) p.(=)


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