chr6:32358268:G>A Detail (hg38) (TSBP1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr6:32,326,045-32,326,045 View the variant detail on this assembly version. |
hg38 | chr6:32,358,268-32,358,268 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_006781.4:c.218-2599C>T | |
NM_001286475.1:c.197-2599C>T | ||
NM_001286474.1:c.218-2599C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.434 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
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 |
---|---|---|---|---|---|
0.007 | Diabetes Mellitus, Insulin-Dependent | NA | GAD | Detail |
Annotation
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs2395150 dbSNP
- Genome
- hg38
- Position
- chr6:32,358,268-32,358,268
- 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))
- rs2395150
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4342
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 7277
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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