Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGCAGTGGAAGAGATGATTCCTGC[A/G]ATGAGCCCAAATCCCCTTGAGATTC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 611049 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC17A2 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | CHB (Han Chinese)
|
||||||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
SLC17A2 - solute carrier family 17 member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286123.1 | 1642 | Silent Mutation | ATC,ATT | I,I 419 | NP_001273052.1 | |
NM_001286125.1 | 1642 | Missense Mutation | TCG,TTG | S,L 370 | NP_001273054.1 | |
NM_005835.3 | 1642 | Missense Mutation | TCG,TTG | S,L 370 | NP_005826.1 | |
XM_005248784.2 | 1642 | Silent Mutation | ATC,ATT | I,I 419 | XP_005248841.1 | |
XM_006714949.3 | 1642 | Silent Mutation | ATC,ATT | I,I 419 | XP_006715012.1 | |
XM_006714950.2 | 1642 | Silent Mutation | ATC,ATT | I,I 396 | XP_006715013.1 | |
XM_006714951.1 | 1642 | Missense Mutation | TCG,TTG | S,L 370 | XP_006715014.1 | |
XM_017010159.1 | 1642 | Silent Mutation | ATC,ATT | I,I 396 | XP_016865648.1 | |
XM_017010160.1 | 1642 | Intron | XP_016865649.1 |
Set Membership: |
HapMap |