Product Details
- SNP ID
-
rs116401889
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:42417950 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTTGCGGGAGCGGATCCAGCCCAC[A/G]GCCACCACCGAGCCCACCTGTGGGA
- Phenotype
-
MIM: 158378
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC20A2
PubMed Links
Gene Details
- Gene
- SLC20A2
- Gene Name
- solute carrier family 20 member 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001257180.1 |
2244 |
Silent Mutation |
GCC,GCT |
A604A |
NP_001244109.1 |
NM_001257181.1 |
2244 |
Silent Mutation |
GCC,GCT |
A604A |
NP_001244110.1 |
NM_006749.4 |
2244 |
Silent Mutation |
GCC,GCT |
A604A |
NP_006740.1 |
XM_005273613.3 |
2244 |
Silent Mutation |
GCC,GCT |
A604A |
XP_005273670.1 |
XM_005273615.3 |
2244 |
UTR 3 |
|
|
XP_005273672.1 |
XM_006716390.3 |
2244 |
Silent Mutation |
GCC,GCT |
A557A |
XP_006716453.1 |
XM_006716391.3 |
2244 |
Silent Mutation |
GCC,GCT |
A467A |
XP_006716454.1 |
XM_017013748.1 |
2244 |
Silent Mutation |
GCC,GCT |
A604A |
XP_016869237.1 |
XM_017013749.1 |
2244 |
Silent Mutation |
GCC,GCT |
A557A |
XP_016869238.1 |
XM_017013750.1 |
2244 |
Silent Mutation |
GCC,GCT |
A467A |
XP_016869239.1 |
XM_017013751.1 |
2244 |
Silent Mutation |
GCC,GCT |
A467A |
XP_016869240.1 |
XM_017013752.1 |
2244 |
Silent Mutation |
GCC,GCT |
A467A |
XP_016869241.1 |
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