chr16:3243403:T>A Detail (hg38) (MEFV, LOC126862264)

Information

Genome

Assembly Position
hg19 chr16:3,293,403-3,293,403 View the variant detail on this assembly version.
hg38 chr16:3,243,403-3,243,403

HGVS

Type Transcript Protein
RefSeq NM_000243.2:c.2084A>T NP_000234.1:p.Lys695Met
NM_001198536.1:c.*288A>T
Ensemble ENST00000219596.6:c.2084A>T ENST00000219596.6:p.Lys695Met
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Uncertain significance
Review star
Show details
Links
Type Database ID Link
Gene MIM 608107 OMIM
HGNC 6998 HGNC
Ensembl ENSG00000103313 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Uncertain significance 2019-05-28 criteria provided, single submitter familial Mediterranean fever not provided unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.753 familial Mediterranean fever NA CLINVAR Detail
0.064 amyloidosis We compared the frequencies of seven MEFV mutations (M694V, M680I, V726A, M694I,... BeFree 11029479 Detail
0.753 familial Mediterranean fever Mutational analysis of the PRYSPRY domain of pyrin and implications for familial... UNIPROT 16730661 Detail
0.753 familial Mediterranean fever MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever. UNIPROT 10612841 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000243.3(MEFV):c.2084A>T (p.Lys695Met) AND Familial Mediterranean fever ClinVar Detail
NA DisGeNET Detail
We compared the frequencies of seven MEFV mutations (M694V, M680I, V726A, M694I, K695R, R761H, E148Q... DisGeNET Detail
Mutational analysis of the PRYSPRY domain of pyrin and implications for familial mediterranean fever... DisGeNET Detail
MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever. DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs104895094 dbSNP
Genome
hg38
Position
chr16:3,243,403-3,243,403
Variant Type
snv
Reference Allele
T
Alternative Allele
A
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