chr21:31667271:T>C Detail (hg38) (SOD1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr21:33,039,584-33,039,584 View the variant detail on this assembly version. |
hg38 | chr21:31,667,271-31,667,271 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000454.4:c.253T>C | NP_000445.1:p.Leu85= |
Ensemble | ENST00000270142.11:c.253T>C | ENST00000270142.11:p.Leu85= |
ENST00000389995.4:c.196T>C | ENST00000389995.4:p.Leu66= |
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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2022-06-01 | criteria provided, single submitter | not provided |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.520 | AMYOTROPHIC LATERAL SCLEROSIS 1 | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000454.5(SOD1):c.253T>C (p.Leu85=) AND not provided | 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
- -
- Genome
- hg38
- Position
- chr21:31,667,271-31,667,271
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
- Heterozygous Counts in All Race (ExAC)
- 1
- East Asian Chromosome Counts (ExAC)
- 8608
- 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)
- 120754
- Allele Counts in All Race (ExAC)
- 1
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 8.281299170213822E-6
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