Variant #0000000542 (NC_000016.9:g.3293403T>C, NM_000243.2:c.2084A>G (MEFV))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.3293403T>C
Reference -
DB-ID MEFV_000019
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00532 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 13:54:05 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEFV NM_000243.2 +/+ 10 c.2084A>G r.(?) p.(Lys695Arg)