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GTGCAATTTCTTACATAAGATTTCC[C/G]TAAACGGCTGGCATAGAAAGAAATA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611318 MIM: 610116 | |||||||||||||||||||||||
Literature Links: |
GPR171 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
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 |
GPR171 - G protein-coupled receptor 171 | ||||||
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There are no transcripts associated with this gene. |
MED12L - mediator complex subunit 12 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_053002.5 | 1196 | Intron | NP_443728.3 | |||
XM_006713487.3 | 1196 | Intron | XP_006713550.1 | |||
XM_011512390.2 | 1196 | Intron | XP_011510692.1 | |||
XM_011512394.2 | 1196 | Intron | XP_011510696.1 | |||
XM_011512399.2 | 1196 | Intron | XP_011510701.1 | |||
XM_017005676.1 | 1196 | Intron | XP_016861165.1 | |||
XM_017005677.1 | 1196 | Intron | XP_016861166.1 | |||
XM_017005678.1 | 1196 | Intron | XP_016861167.1 | |||
XM_017005679.1 | 1196 | Intron | XP_016861168.1 | |||
XM_017005680.1 | 1196 | Intron | XP_016861169.1 | |||
XM_017005681.1 | 1196 | Intron | XP_016861170.1 |
P2RY14 - purinergic receptor P2Y14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001081455.1 | 1196 | Missense Mutation | ACG,AGG | T,R 303 | NP_001074924.1 | |
NM_014879.3 | 1196 | Missense Mutation | ACG,AGG | T,R 303 | NP_055694.3 | |
XM_005247922.3 | 1196 | Missense Mutation | ACG,AGG | T,R 303 | XP_005247979.1 | |
XM_005247923.3 | 1196 | Missense Mutation | ACG,AGG | T,R 303 | XP_005247980.1 | |
XM_011513340.2 | 1196 | Missense Mutation | ACG,AGG | T,R 303 | XP_011511642.1 | |
XM_017007583.1 | 1196 | Missense Mutation | ACG,AGG | T,R 303 | XP_016863072.1 |