Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603080 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC6A12 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
|
SLC6A12 - solute carrier family 6 member 12 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122847.2 | 2552 | Missense Mutation | ACC,GCC | T,A 598 | NP_001116319.1 | |
NM_001122848.2 | 2552 | Missense Mutation | ACC,GCC | T,A 598 | NP_001116320.1 | |
NM_001206931.1 | 2552 | Missense Mutation | ACC,GCC | T,A 598 | NP_001193860.1 | |
NM_003044.4 | 2552 | Missense Mutation | ACC,GCC | T,A 598 | NP_003035.3 | |
XM_005253747.4 | 2552 | Intron | XP_005253804.1 | |||
XM_005253748.4 | 2552 | UTR 3 | XP_005253805.1 | |||
XM_006719005.3 | 2552 | Intron | XP_006719068.1 | |||
XM_011521010.1 | 2552 | Missense Mutation | ACC,GCC | T,A 598 | XP_011519312.1 | |
XM_017019841.1 | 2552 | Missense Mutation | ACC,GCC | T,A 410 | XP_016875330.1 |