Variant #0000000544 (NC_000016.9:g.3293257C>A, NM_000243.2:c.2230G>T (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.3293257C>A
Reference -
DB-ID MEFV_000021
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00184 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 13:54:57 +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.2230G>T r.(?) p.(Ala744Ser)