Search
LOADING 
- SNP ID:
- rs140479354
- Gene
-
SLC12A9 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.7: 100855836 - 100855836 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
AGTCTGTGCTTGATGTCTTCGGGGC[C/T]GGTCTGTGCTCTGTCCGATCTGGGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 616861
|
||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC12A9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| SLC12A9 - solute carrier family 12 member 9 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001267812.1 | 607 | Silent Mutation | GCC,GCT | A,A 149 | NP_001254741.1 | |
| NM_001267814.1 | 607 | Intron | NP_001254743.1 | |||
| NM_020246.3 | 607 | Silent Mutation | GCC,GCT | A,A 149 | NP_064631.2 | |
| XM_005250502.2 | 607 | Intron | XP_005250559.1 | |||
| XM_005250504.4 | 607 | Intron | XP_005250561.1 | |||
| XM_006716054.2 | 607 | Intron | XP_006716117.1 | |||
| XM_006716055.2 | 607 | Silent Mutation | GCC,GCT | A,A 149 | XP_006716118.1 | |
| XM_011516414.1 | 607 | Intron | XP_011514716.1 | |||
Back To Top