Variant #0000879677 (NC_000011.9:g.63974955C>T, NM_031471.5:c.119C>T (FERMT3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.63974955C>T
DNA change (hg38) g.64207483C>T
Published as -
ISCN -
DB-ID FERMT3_000056
Variant remarks -
Reference PubMed: Roos 2023, Journal: Roos 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Dirk Roos
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-09-27 17:12:21 +02:00 (CEST)
Date last edited 2025-01-23 20:45:08 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FERMT3 NM_031471.5 -/. - c.119C>T r.(?) p.(Ser40Leu)


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