Product Details
- SNP ID
-
rs140355561
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:27256802 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCGACTCACCTTCCATGAGGATT[C/G]GAAGAACGTCTCGGAGGGTGGGAGC
- Phenotype
-
MIM: 602878
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SLC30A3
PubMed Links
Gene Details
- Gene
- SLC30A3
- Gene Name
- solute carrier family 30 member 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001318949.1 |
912 |
Missense Mutation |
CCA,CGA |
P285R |
NP_001305878.1 |
NM_001318950.1 |
912 |
Missense Mutation |
CCA,CGA |
P277R |
NP_001305879.1 |
NM_001318951.1 |
912 |
Missense Mutation |
CCA,CGA |
P277R |
NP_001305880.1 |
NM_003459.4 |
912 |
Missense Mutation |
CCA,CGA |
P290R |
NP_003450.2 |
XM_005264547.1 |
912 |
Missense Mutation |
CAA,GAA |
Q239E |
XP_005264604.1 |
XM_005264548.3 |
912 |
Missense Mutation |
CAA,GAA |
Q234E |
XP_005264605.1 |
XM_006712100.2 |
912 |
Missense Mutation |
CAA,GAA |
Q190E |
XP_006712163.1 |
XM_011533102.2 |
912 |
Missense Mutation |
CCA,CGA |
P217R |
XP_011531404.1 |
XM_011533103.2 |
912 |
Missense Mutation |
CCA,CGA |
P176R |
XP_011531405.1 |
XM_017004873.1 |
912 |
Missense Mutation |
CAA,GAA |
Q226E |
XP_016860362.1 |
XM_017004874.1 |
912 |
Missense Mutation |
CAA,GAA |
Q226E |
XP_016860363.1 |
XM_017004875.1 |
912 |
Missense Mutation |
CAA,GAA |
Q217E |
XP_016860364.1 |
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