chr11:67586108:> Detail (hg38) (GSTP1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:67,353,579-67,353,579 |
hg38 | chr11:67,586,108-67,586,108 |
HGVS
Type | Transcript | Protein |
---|---|---|
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2010-12-30 | no assertion criteria provided | GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE A |
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Detail |
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1997-04-11 | no assertion criteria provided | GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE B |
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Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000852.4(GSTP1):c.[313=;341=] AND GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE A | ClinVar | Detail |
NM_000852.4(GSTP1):c.[313A>G;341=] AND GLUTATHIONE S-TRANSFERASE PI POLYMORPHISM, TYPE B | ClinVar | 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
- chr11:67,586,108-67,586,108
- Variant Type
- snv
Genome browser