Variant #0000000528 (NC_000016.9:g.3304626C>G, NM_000243.2:c.442G>C (MEFV))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.3304626C>G
Reference -
DB-ID MEFV_000006
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0708 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 13:42:24 +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 ?/? 2 c.442G>C r.(?) p.(Glu148Gln)