Variant #0000000535 (NC_000016.9:g.3293880A>G, NM_000243.2:c.1772T>C (MEFV))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.3293880A>G
Reference -
DB-ID MEFV_000013
Frequency -
Average frequency (gnomAD v.2.1.1) 0.01063 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-05-07 13:47:27 +00:00 (UTC)
Date last edited 2025-07-29 10:41:25 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
MEFV NM_000243.2 -?/-? 9 c.1772T>C r.(?) p.(Ile591Thr) likely benign