Product Details
- SNP ID
-
rs143032407
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.21:31120498 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGCTTGCTTCTTGAGCTGTGCCATG[C/T]GGGACGCGTGACTATCCAGGGTTTT
- Phenotype
-
MIM: 600687
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TIAM1
PubMed Links
Gene Details
- Gene
- TIAM1
- Gene Name
- T-cell lymphoma invasion and metastasis 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003253.2 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
NP_003244.2 |
XM_005261037.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_005261094.1 |
XM_005261038.2 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_005261095.1 |
XM_005261040.2 |
5182 |
UTR 3 |
|
|
XP_005261097.1 |
XM_011529711.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_011528013.1 |
XM_011529712.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_011528014.1 |
XM_011529713.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_011528015.1 |
XM_017028447.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883936.1 |
XM_017028448.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883937.1 |
XM_017028449.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883938.1 |
XM_017028450.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883939.1 |
XM_017028451.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883940.1 |
XM_017028452.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883941.1 |
XM_017028453.1 |
5182 |
Missense Mutation |
CAC,CGC |
H1549R |
XP_016883942.1 |
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