Variant #0000679536 (NC_000012.11:g.48527131G>C, PFKM(NM_000289.5):c.461G>C)

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.48527131G>C
DNA change (hg38) -
Published as PFKM(NM_001354736.1):c.770G>C (p.S257T)
ISCN -
DB-ID PFKM_000012
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKM NM_000289.5 ?/. - c.461G>C r.(?) p.(Ser154Thr)
PFKM NM_001166686.1 ?/. - c.674G>C r.(?) p.(Ser225Thr)
SENP1 NM_001267594.1 ?/. - c.-27365C>G r.(?) p.(=)