Variant #0000725761 (NC_000016.9:g.3293447C>G, NM_000243.2:c.2040G>C (MEFV))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3293447C>G
DNA change (hg38) -
Published as MEFV(NM_000243.2):c.2040G>C (p.M680I), MEFV(NM_000243.3):c.2040G>C (p.(Met680Ile), p.M680I)
ISCN -
DB-ID MEFV_000012 See all 35 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00011 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEFV NM_000243.2 +/. - c.2040G>C r.(?) p.(Met680Ile)


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