chr21:33040830:G>A Detail (hg19) (SOD1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr21:33,040,830-33,040,830 |
hg38 | chr21:31,668,517-31,668,517 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000454.4:c.404G>A | NP_000445.1:p.Ser135Asn |
Ensemble | ENST00000270142.11:c.404G>A | ENST00000270142.11:p.Ser135Asn |
ENST00000389995.4:c.347G>A | ENST00000389995.4:p.Ser116Asn |
Summary
MGeND
Clinical significance |
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Variant entry | 1 |
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 |
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Review star | ![]() |
Show details |
Disease area statistics
MGeND
Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
---|---|---|---|---|---|---|---|---|---|
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amyotrophic lateral sclerosis |
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MGS000082
(TMGS000165) |
Kenjiro Kosaki Kenjiro Kosaki |
Keio University Mutation View |
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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1997-01-01 | no assertion criteria provided | amyotrophic lateral sclerosis type 1 |
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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 | |
0.438 | amyotrophic lateral sclerosis | Analysis of the 35 patients with sporadic ALS revealed a previously known SOD1 m... | BeFree | 18852346 | Detail |
0.520 | AMYOTROPHIC LATERAL SCLEROSIS 1 | S134N copper-zinc superoxide dismutase (SOD1) is one of the many mutant SOD1 pro... | BeFree | 16105836 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000454.5(SOD1):c.404G>A (p.Ser135Asn) AND Amyotrophic lateral sclerosis type 1 | ClinVar | Detail |
NA | DisGeNET | Detail |
Analysis of the 35 patients with sporadic ALS revealed a previously known SOD1 mutation, S134N, a no... | DisGeNET | Detail |
S134N copper-zinc superoxide dismutase (SOD1) is one of the many mutant SOD1 proteins known to cause... | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
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Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs121912451 dbSNP
- Genome
- hg19
- Position
- chr21:33,040,830-33,040,830
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
- 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))
- rs121912451
- 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))
- 2
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 8652
- 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)
- 121354
- 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)
- 8.240354664864776E-6
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