Product Details
- SNP ID
-
rs139960065
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:90885130 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGAGGCCGAGCTTCGTCTACTGGAG[C/G]GCATGAGAAAGTGGATGGCCCAGCG
- Phenotype
-
MIM: 190030
MIM: 136950
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
FES
PubMed Links
Gene Details
- Gene
- FES
- Gene Name
- FES proto-oncogene, tyrosine kinase
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001143783.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
NP_001137255.1 |
| NM_001143784.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
NP_001137256.1 |
| NM_001143785.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
NP_001137257.1 |
| NM_002005.3 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
NP_001996.1 |
| XM_005254880.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_005254937.1 |
| XM_005254882.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_005254939.1 |
| XM_017022005.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_016877494.1 |
| XM_017022006.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_016877495.1 |
| XM_017022007.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_016877496.1 |
| XM_017022008.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_016877497.1 |
| XM_017022009.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_016877498.1 |
| XM_017022010.1 |
212 |
Missense Mutation |
CGC,GGC |
R29G |
XP_016877499.1 |
- Gene
- FURIN
- Gene Name
- furin, paired basic amino acid cleaving enzyme
There are no transcripts associated with this gene.
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