Genomic variant #0000088243

Individual ID 00057936
Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.3293407T>C
DNA change (hg38) g.3243407T>C
Published as -
ISCN -
DB-ID MEFV_000008 See all 55 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00023 View details
Owner Wided Kelmemi




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
MEFV NM_000243.2 +?/. 10 c.2080A>G - r.(?) p.(Met694Val)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000057899 DNA SEQ White Blood Cells - MEFV 2 Wided Kelmemi