Product Details
- SNP ID
-
rs188539443
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
5
- Location
-
Chr.1:94824529 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGGCTACTCGGTGGTGGCTGGAGCC[A/G]CGGGAAGACTCCTCTTTGGCTATGA
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
LINC01057
PubMed Links
Gene Details
- Gene
- LINC01057
- Gene Name
- long intergenic non-protein coding RNA 1057
There are no transcripts associated with this gene.
- Gene
- SLC44A3
- Gene Name
- solute carrier family 44 member 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001114106.2 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
NP_001107578.1 |
NM_001258340.1 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
NP_001245269.1 |
NM_001258341.1 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
NP_001245270.1 |
NM_001258342.1 |
174 |
Missense Mutation |
ACG,GCG |
T22A |
NP_001245271.1 |
NM_001258343.1 |
174 |
Missense Mutation |
ACG,GCG |
T22A |
NP_001245272.1 |
NM_001301079.1 |
174 |
Missense Mutation |
ACG,GCG |
T10A |
NP_001288008.1 |
NM_152369.4 |
174 |
Missense Mutation |
ACG,GCG |
T10A |
NP_689582.2 |
XM_005270440.2 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_005270497.1 |
XM_005270441.2 |
174 |
Missense Mutation |
ACG,GCG |
T10A |
XP_005270498.1 |
XM_005270442.1 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_005270499.1 |
XM_011540632.2 |
174 |
UTR 5 |
|
|
XP_011538934.1 |
XM_011540633.2 |
174 |
Intron |
|
|
XP_011538935.1 |
XM_011540635.2 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_011538937.1 |
XM_011540636.2 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_011538938.1 |
XM_017000262.1 |
174 |
Missense Mutation |
ACG,GCG |
T22A |
XP_016855751.1 |
XM_017000263.1 |
174 |
Missense Mutation |
ACG,GCG |
T10A |
XP_016855752.1 |
XM_017000264.1 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_016855753.1 |
XM_017000265.1 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_016855754.1 |
XM_017000266.1 |
174 |
Missense Mutation |
ACG,GCG |
T58A |
XP_016855755.1 |
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