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TGGTAGAGTTCTGAATGCCGTTTCC[A/G]GGTGTGCATCACCTTCTAGGGGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
MIM: 602683 | ||||||||||||||||||||
Literature Links: |
ADGRB2 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 |
ADGRB2 - adhesion G protein-coupled receptor B2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001294335.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1477 | NP_001281264.1 | |
NM_001294336.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1444 | NP_001281265.1 | |
XM_011541848.2 | 4855 | Missense Mutation | CGG,TGG | R,W 1478 | XP_011540150.1 | |
XM_011541849.2 | 4855 | Missense Mutation | CGG,TGG | R,W 1466 | XP_011540151.1 | |
XM_011541858.2 | 4855 | Missense Mutation | CGG,TGG | R,W 1175 | XP_011540160.1 | |
XM_017001899.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1478 | XP_016857388.1 | |
XM_017001900.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1477 | XP_016857389.1 | |
XM_017001901.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1478 | XP_016857390.1 | |
XM_017001902.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1477 | XP_016857391.1 | |
XM_017001903.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1455 | XP_016857392.1 | |
XM_017001904.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1445 | XP_016857393.1 | |
XM_017001905.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1444 | XP_016857394.1 | |
XM_017001906.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1445 | XP_016857395.1 | |
XM_017001907.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1423 | XP_016857396.1 | |
XM_017001908.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1423 | XP_016857397.1 | |
XM_017001909.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1423 | XP_016857398.1 | |
XM_017001910.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1390 | XP_016857399.1 | |
XM_017001911.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1390 | XP_016857400.1 | |
XM_017001912.1 | 4855 | Missense Mutation | CGG,TGG | R,W 1368 | XP_016857401.1 |