Variant #0001016621 (NC_000012.11:g.48531630G>A, NC_000012.11(NM_000289.5):c.1062+1G>A (PFKM))

Chromosome 12
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.48531630G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PFKM_000019
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs766042700
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-11-07 18:31:01 +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.1062+1G>A r.(?) p.(?)


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