Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCAAGGGTCTGGAGAACATGGGG[C/G]CTGATTTCTTGGAAAGCCTGGTCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 606207 | ||||||||||||||||||||
Literature Links: |
SLC28A1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SLC28A1 - solute carrier family 28 member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287761.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | NP_001274690.1 | |
NM_001287762.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | NP_001274691.1 | |
NM_001321721.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | NP_001308650.1 | |
NM_001321722.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | NP_001308651.1 | |
NM_004213.4 | 493 | Missense Mutation | CCT,GCT | P,A 26 | NP_004204.3 | |
NM_201651.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | NP_964014.1 | |
XM_011522203.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520505.1 | |
XM_011522204.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520506.1 | |
XM_011522205.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520507.1 | |
XM_011522206.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520508.1 | |
XM_011522207.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520509.1 | |
XM_011522208.2 | 493 | Silent Mutation | GGC,GGG | G,G 46 | XP_011520510.1 | |
XM_011522209.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520511.1 | |
XM_011522210.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520512.1 | |
XM_011522211.2 | 493 | UTR 5 | XP_011520513.1 | |||
XM_011522212.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520514.1 | |
XM_011522214.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520516.1 | |
XM_011522215.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520517.1 | |
XM_011522216.2 | 493 | UTR 5 | XP_011520518.1 | |||
XM_011522217.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520519.1 | |
XM_011522218.2 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_011520520.1 | |
XM_017022723.1 | 493 | Missense Mutation | CCT,GCT | P,A 26 | XP_016878212.1 |