Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 611318 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GPR171 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 | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
GPR171 - G protein-coupled receptor 171 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013308.3 | 1087 | Missense Mutation | ATC,GTC | I,V 283 | NP_037440.3 | |
XM_005247402.3 | 1087 | Missense Mutation | ATC,GTC | I,V 283 | XP_005247459.1 | |
XM_005247403.3 | 1087 | Missense Mutation | ATC,GTC | I,V 283 | XP_005247460.1 | |
XM_017006274.1 | 1087 | Missense Mutation | ATC,GTC | I,V 283 | XP_016861763.1 |
MED12L - mediator complex subunit 12 like | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_053002.5 | 1087 | Intron | NP_443728.3 | |||
XM_006713487.3 | 1087 | Intron | XP_006713550.1 | |||
XM_011512390.2 | 1087 | Intron | XP_011510692.1 | |||
XM_011512394.2 | 1087 | Intron | XP_011510696.1 | |||
XM_011512399.2 | 1087 | Intron | XP_011510701.1 | |||
XM_017005676.1 | 1087 | Intron | XP_016861165.1 | |||
XM_017005677.1 | 1087 | Intron | XP_016861166.1 | |||
XM_017005678.1 | 1087 | Intron | XP_016861167.1 | |||
XM_017005679.1 | 1087 | Intron | XP_016861168.1 | |||
XM_017005680.1 | 1087 | Intron | XP_016861169.1 | |||
XM_017005681.1 | 1087 | Intron | XP_016861170.1 |
Set Membership: |
HapMap |