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ATTTCACAGTAGGGCCGGTGGCAGC[A/G]GCAGAAGAACTCATCTGAGCTGCTG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610464 | |||||||||||||||||||||||
Literature Links: |
GPR156 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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 |
GPR156 - G protein-coupled receptor 156 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168271.1 | 2731 | Missense Mutation | CGC,TGC | R,C 753 | NP_001161743.1 | |
NM_153002.2 | 2731 | Missense Mutation | CGC,TGC | R,C 757 | NP_694547.2 | |
XM_005247165.2 | 2731 | Missense Mutation | CGC,TGC | R,C 757 | XP_005247222.1 | |
XM_011512484.2 | 2731 | Missense Mutation | CGC,TGC | R,C 676 | XP_011510786.1 | |
XM_011512487.1 | 2731 | Missense Mutation | CGC,TGC | R,C 676 | XP_011510789.1 | |
XM_011512488.2 | 2731 | Missense Mutation | CGC,TGC | R,C 371 | XP_011510790.1 | |
XM_017005795.1 | 2731 | Missense Mutation | CGC,TGC | R,C 757 | XP_016861284.1 | |
XM_017005796.1 | 2731 | Missense Mutation | CGC,TGC | R,C 757 | XP_016861285.1 | |
XM_017005797.1 | 2731 | Missense Mutation | CGC,TGC | R,C 753 | XP_016861286.1 |