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GTAATCATAATATATGCGAACTTCC[G/T]ATCTTCTCACACTTTGCAGTGATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606379 MIM: 611318 | ||||||||||||||||||||
Literature Links: |
GPR87 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
GPR87 - G protein-coupled receptor 87 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023915.3 | 1401 | Missense Mutation | TGG,TTG | W,L 347 | NP_076404.3 |
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 | 1401 | Intron | NP_443728.3 | |||
XM_006713487.3 | 1401 | Intron | XP_006713550.1 | |||
XM_011512390.2 | 1401 | Intron | XP_011510692.1 | |||
XM_011512394.2 | 1401 | Intron | XP_011510696.1 | |||
XM_011512399.2 | 1401 | Intron | XP_011510701.1 | |||
XM_017005676.1 | 1401 | Intron | XP_016861165.1 | |||
XM_017005677.1 | 1401 | Intron | XP_016861166.1 | |||
XM_017005678.1 | 1401 | Intron | XP_016861167.1 | |||
XM_017005679.1 | 1401 | Intron | XP_016861168.1 | |||
XM_017005680.1 | 1401 | Intron | XP_016861169.1 | |||
XM_017005681.1 | 1401 | Intron | XP_016861170.1 |