Variant #0000980281 (NC_000012.11:g.48526634T>A, NC_000012.11(NM_000289.5):c.238-17T>A (PFKM))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48526634T>A
DNA change (hg38) -
Published as PFKM(NM_000289.6):c.238-17T>A
ISCN -
DB-ID PFKM_000018
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) 8.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
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.238-17T>A r.(=) p.(=)
PFKM NM_001166686.1 -?/. - c.451-17T>A r.(=) p.(=)
SENP1 NM_001267594.1 -?/. - c.-26868A>T r.(?) p.(=)


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