Product Details
- SNP ID
-
rs1062633
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:49887507 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TGCTCCACCTCCCCCACTAGTACTC[C/T]GAAGGTGGGTCGCACTGCTGGGTCT
- Phenotype
-
MIM: 600168
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
MST1R
PubMed Links
Gene Details
- Gene
- MST1R
- Gene Name
- macrophage stimulating 1 receptor
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001244937.2 |
4029 |
Missense Mutation |
AGA,GGA |
R1286G |
NP_001231866.1 |
NM_001318913.1 |
4029 |
Missense Mutation |
AGA,GGA |
R1229G |
NP_001305842.1 |
NM_002447.3 |
4029 |
Missense Mutation |
AGA,GGA |
R1335G |
NP_002438.2 |
XM_005265170.4 |
4029 |
Missense Mutation |
AGA,GGA |
R1336G |
XP_005265227.2 |
XM_011533739.2 |
4029 |
Missense Mutation |
AGA,GGA |
R1296G |
XP_011532041.1 |
XM_011533740.2 |
4029 |
Missense Mutation |
AGA,GGA |
R1287G |
XP_011532042.1 |
XM_011533741.2 |
4029 |
Missense Mutation |
AGA,GGA |
R1267G |
XP_011532043.1 |
XM_011533742.2 |
4029 |
Missense Mutation |
CAG,CGG |
Q1290R |
XP_011532044.1 |
XM_011533743.2 |
4029 |
Missense Mutation |
AGA,GGA |
R1235G |
XP_011532045.1 |
XM_011533744.2 |
4029 |
Missense Mutation |
AGA,GGA |
R1230G |
XP_011532046.1 |
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