chr16:3243529:C>T Detail (hg38) (MEFV, LOC126862264)

Information

Genome

Assembly Position
hg19 chr16:3,293,529-3,293,529 View the variant detail on this assembly version.
hg38 chr16:3,243,529-3,243,529

HGVS

Type Transcript Protein
RefSeq NM_000243.2:c.1958G>A NP_000234.1:p.Arg653His
NM_001198536.1:c.*162G>A
Ensemble ENST00000219596.6:c.1958G>A ENST00000219596.6:p.Arg653His
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:<0.001
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Conflicting classifications of pathogenicity
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 tgv54446009 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Conflicting interpretations of pathogenicity 2024-01-27 criteria provided, conflicting interpretations familial Mediterranean fever germline not provided unknown Detail
Pathogenic Likely pathogenic 2021-02-18 criteria provided, multiple submitters, no conflicts not provided germline Detail
Likely pathogenic 2023-10-24 criteria provided, single submitter Familial Mediterranean fever, autosomal dominant unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.753 familial Mediterranean fever NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000243.3(MEFV):c.1958G>A (p.Arg653His) AND Familial Mediterranean fever ClinVar Detail
NM_000243.3(MEFV):c.1958G>A (p.Arg653His) AND not provided ClinVar Detail
NM_000243.3(MEFV):c.1958G>A (p.Arg653His) AND Familial Mediterranean fever, autosomal dominant ClinVar Detail
NA 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
rs104895085 dbSNP
Genome
hg38
Position
chr16:3,243,529-3,243,529
Variant Type
snv
Reference Allele
C
Alternative Allele
T
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs104895085
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0001
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
8654
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
121204
Allele Counts in All Race (ExAC)
6
Heterozygous Counts in All Race (ExAC)
6
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
4.950331672222039E-5
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