Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | NTRK2 |
Variant | E371D |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | NTRK2 E371D lies within the extracellular domain of the Ntrk2 protein (UniProt.org). E371D has not been characterized in the scientific literature and therefore, its effect on Ntrk2 protein function is unknown (PubMed, Mar 2025). |
Associated Drug Resistance | |
Category Variants Paths |
NTRK2 mutant NTRK2 E371D |
Transcript | NM_001018064.3 |
gDNA | chr9:g.84727913G>C |
cDNA | c.1113G>C |
Protein | p.E371D |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001007097 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001007097.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001007097.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018064 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018064.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018064.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018065 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018065.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018065.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018066 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018066.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001018066.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369532.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369533.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369534.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369537.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369538.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369539.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369540.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369541.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369542.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369543.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369544.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369545.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369547.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369548.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_001369549.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_006180 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_006180.4 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
NM_006180.6 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252001 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252001.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252001.4 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252003 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252003.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252003.4 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252004 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252004.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252004.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252006 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252006.4 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252007 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_005252007.4 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_011518718 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_011518718.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_011518718.4 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_011518720 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_011518720.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014751 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014751.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014751.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014752 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014752.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014752.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014753 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014753.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014753.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014754 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014754.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014755 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014755.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014755.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014756 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014756.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014757 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014757.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014758 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014758.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014759 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014759.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014760 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014760.2 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014760.3 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014761 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_017014761.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_047423432.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
XM_047423433.1 | chr9:g.84727913G>C | c.1113G>C | p.E371D | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
No data available in table |
CKB CORE allows for only a limited number of monthly page views for un-registered users. However, registration is free and allows for unlimited browsing of the CKB CORE content.
You have reached the monthly page view limit. For continued free access to CKB CORE, please register below: