chr9:87339190:G>A Detail (hg19) (NTRK2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr9:87,339,190-87,339,190 |
hg38 | chr9:84,724,275-84,724,275 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001018065.2:c.772G>A | NP_001018075.1:p.Asp258Asn |
NM_001018064.2:c.772G>A | NP_001018074.1:p.Asp258Asn | |
NM_001018066.2:c.772G>A | NP_001018076.1:p.Asp258Asn |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_006180.6(NTRK2):c.772G>A (p.Asp258Asn) AND not provided | ClinVar | Detail |
NM_006180.6(NTRK2):c.772G>A (p.Asp258Asn) AND NTRK2-related disorder | 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
- hg19
- Position
- chr9:87,339,190-87,339,190
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
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