Variant #0000018011 (NC_000003.11:g.196733596C>T, NM_005929.5:c.1762G>A (MFI2))

Chromosome 3
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.196733596C>T
DNA change (hg38) g.197006725C>T
Published as -
ISCN -
DB-ID MFI2_000006
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00083 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-08 23:53:32 +02:00 (CEST)
Date last edited 2024-03-26 14:54:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFI2 NM_005929.5 ?/? ? c.1762G>A r.(?) p.(Glu588Lys)



Screenings

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