chr12:102174359:TCTG> Detail (hg19) (GNPTAB)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr12:102,174,359-102,174,362 |
hg38 | chr12:101,780,581-101,780,584 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_024312.4:c.609_612delCAGA | NP_077288.2:p.Thr206TyrfsTer6 |
Ensemble | ENST00000299314.12:c.609_612delCAGA | ENST00000299314.12:p.Thr206TyrfsTer6 |
ENST00000549940.5:c.609_612delCAGA | ENST00000549940.5:p.Thr206TyrfsTer6 |
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 | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.441 | MUCOLIPIDOSIS II ALPHA/BETA (disorder) | NA | CLINVAR | Detail |
Annotation
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
- hg19
- Position
- chr12:102,174,359-102,174,362
- Variant Type
- snv
- Reference Allele
- TCTG
- Alternative Allele
- -
- East Asian Chromosome Counts (ExAC)
- 8560
- 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)
- 118742
- Allele Counts in All Race (ExAC)
- 5
- Heterozygous Counts in All Race (ExAC)
- 5
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 4.210809991409948E-5
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