Product Details
- SNP ID
-
rs139894245
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
5
- Location
-
Chr.1:156807268 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGTGGGGGAGGGTGTGTCTCCAGGC[A/G]GGTGGGGGCTGGTGGGGCAGGGGAG
- Phenotype
-
MIM: 191315
MIM: 179755
MIM: 604514
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NTRK1
PubMed Links
Gene Details
- Gene
- NTRK1
- Gene Name
- neurotrophic receptor tyrosine kinase 1
There are no transcripts associated with this gene.
- Gene
- PRCC
- Gene Name
- papillary renal cell carcinoma (translocation-associated)
There are no transcripts associated with this gene.
- Gene
- SH2D2A
- Gene Name
- SH2 domain containing 2A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001161441.1 |
1208 |
Silent Mutation |
CCC,CCT |
P370P |
NP_001154913.1 |
NM_001161442.1 |
1208 |
Silent Mutation |
CCC,CCT |
P342P |
NP_001154914.1 |
NM_001161443.1 |
1208 |
Silent Mutation |
CCC,CCT |
P332P |
NP_001154915.1 |
NM_001161444.1 |
1208 |
Silent Mutation |
CCC,CCT |
P360P |
NP_001154916.1 |
NM_003975.3 |
1208 |
Silent Mutation |
CCC,CCT |
P360P |
NP_003966.2 |
XM_006711615.2 |
1208 |
Silent Mutation |
CCC,CCT |
P366P |
XP_006711678.1 |
XM_017002762.1 |
1208 |
Silent Mutation |
CCC,CCT |
P376P |
XP_016858251.1 |
XM_017002763.1 |
1208 |
Silent Mutation |
CCC,CCT |
P372P |
XP_016858252.1 |
XM_017002764.1 |
1208 |
Silent Mutation |
CCC,CCT |
P356P |
XP_016858253.1 |
XM_017002765.1 |
1208 |
Silent Mutation |
CCC,CCT |
P352P |
XP_016858254.1 |
XM_017002766.1 |
1208 |
Silent Mutation |
CCC,CCT |
P348P |
XP_016858255.1 |
XM_017002767.1 |
1208 |
Silent Mutation |
CCC,CCT |
P280P |
XP_016858256.1 |
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