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 |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2020-09-09 | criteria provided, single submitter | TNF receptor-associated periodic fever syndrome (TRAPS) |
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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
Descrption | Source | Links |
---|---|---|
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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