chr7:116783354:A>T Detail (hg38) (MET)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:116,423,408-116,423,408 View the variant detail on this assembly version. |
hg38 | chr7:116,783,354-116,783,354 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001127500.2:c.3737A>T | NP_001120972.1:p.Asp1246Val |
NM_000245.3:c.3683A>T | NP_000236.2:p.Asp1228Val | |
NM_001324402.1:c.3683A>T | NP_001311331.1:p.Asp1228Val |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
---|---|---|---|---|---|---|---|---|---|
lung non-small cell carcinoma | Cabozantinib | C |
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Sensitivity/Response | Somatic | 4 | 27694386 | Detail |
lung non-small cell carcinoma | Savolitinib | C |
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Resistance | Somatic | 4 | 27694386 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Case report of a patient with lung adenocarcinoma harboring both a mutation in EGFR and an amplifica... | CIViC Evidence | Detail |
Case report of a patient with lung adenocarcinoma harboring both a mutation in EGFR and an amplifica... | CIViC Evidence | 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
- chr7:116,783,354-116,783,354
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- T
- Variant (CIViC) (CIViC Variant)
- D1228V
- Transcript 1 (CIViC Variant)
- ENST00000397752.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/798
Genome browser