chr12:6334108:C>G Detail (hg38) (TNFRSF1A)

Information

Genome

Assembly Position
hg19 chr12:6,443,274-6,443,274 View the variant detail on this assembly version.
hg38 chr12:6,334,108-6,334,108

HGVS

Type Transcript Protein
RefSeq NM_001065.3:c.176G>C NP_001056.1:p.Cys59Ser
Ensemble ENST00000162749.7:c.176G>C ENST00000162749.7:p.Cys59Ser
ENST00000440083.7:c.176G>C ENST00000440083.7:p.Cys59Ser
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

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

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 191190 OMIM
HGNC 11916 HGNC
Ensembl ENSG00000067182 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
Pathogenic 2020-09-09 criteria provided, single submitter TNF receptor-associated periodic fever syndrome (TRAPS) germline not provided Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.582 TNF receptor-associated periodic fever syndrome (TRAPS) NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_001065.4(TNFRSF1A):c.176G>C (p.Cys59Ser) AND TNF receptor-associated periodic fever syndrome (TRA... 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
rs104895223 dbSNP
Genome
hg38
Position
chr12:6,334,108-6,334,108
Variant Type
snv
Reference Allele
C
Alternative Allele
G
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)
121412
Allele Counts in All Race (ExAC)
1
Heterozygous Counts in All Race (ExAC)
1
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
8.236418146476461E-6
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