Product Details
- SNP ID
-
rs184194750
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:98797454 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGTGGCTGGTCCAAGGTCCCCCTCC[A/G]CTTCTGCCGAGTGACGGTGATCCAG
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
KIAA1211L
PubMed Links
Gene Details
- Gene
- KIAA1211L
- Gene Name
- KIAA1211 like
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_207362.2 |
2794 |
Missense Mutation |
CGG,TGG |
R834W |
NP_997245.2 |
XM_005263923.3 |
2794 |
Missense Mutation |
CGG,TGG |
R862W |
XP_005263980.1 |
XM_005263924.3 |
2794 |
Missense Mutation |
CGG,TGG |
R862W |
XP_005263981.1 |
XM_005263926.3 |
2794 |
Missense Mutation |
CGG,TGG |
R834W |
XP_005263983.1 |
XM_011511093.1 |
2794 |
Missense Mutation |
CGG,TGG |
R848W |
XP_011509395.1 |
XM_011511094.1 |
2794 |
Missense Mutation |
CGG,TGG |
R834W |
XP_011509396.1 |
XM_011511095.2 |
2794 |
Missense Mutation |
CGG,TGG |
R834W |
XP_011509397.1 |
XM_011511096.1 |
2794 |
Missense Mutation |
CGG,TGG |
R701W |
XP_011509398.1 |
XM_017003971.1 |
2794 |
Missense Mutation |
CGG,TGG |
R848W |
XP_016859460.1 |
XM_017003972.1 |
2794 |
Missense Mutation |
CGG,TGG |
R848W |
XP_016859461.1 |
XM_017003973.1 |
2794 |
Intron |
|
|
XP_016859462.1 |
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