Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAAGAGAGTCCATCTCTCTCACAC[C/T]TGTGGCCAAGGGTCTGGAGAACATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606207 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC28A1 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
|
SLC28A1 - solute carrier family 28 member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287761.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | NP_001274690.1 | |
NM_001287762.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | NP_001274691.1 | |
NM_001321721.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | NP_001308650.1 | |
NM_001321722.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | NP_001308651.1 | |
NM_004213.4 | 464 | Missense Mutation | CCT,CTT | P,L 16 | NP_004204.3 | |
NM_201651.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | NP_964014.1 | |
XM_011522203.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520505.1 | |
XM_011522204.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520506.1 | |
XM_011522205.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520507.1 | |
XM_011522206.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520508.1 | |
XM_011522207.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520509.1 | |
XM_011522208.2 | 464 | Silent Mutation | CTG,TTG | L,L 37 | XP_011520510.1 | |
XM_011522209.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520511.1 | |
XM_011522210.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520512.1 | |
XM_011522211.2 | 464 | UTR 5 | XP_011520513.1 | |||
XM_011522212.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520514.1 | |
XM_011522214.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520516.1 | |
XM_011522215.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520517.1 | |
XM_011522216.2 | 464 | UTR 5 | XP_011520518.1 | |||
XM_011522217.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520519.1 | |
XM_011522218.2 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_011520520.1 | |
XM_017022723.1 | 464 | Missense Mutation | CCT,CTT | P,L 16 | XP_016878212.1 |