Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACGGGAGGAGCCCTCACCTTGGCC[A/G]TGGACTGGCTGCGGTAGCGGTCGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
22 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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 4931 | Missense Mutation | ACG,ATG | T,M 1502 | NP_001281264.1 | |
NM_001294336.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1469 | NP_001281265.1 | |
XM_011541848.2 | 4931 | Missense Mutation | ACG,ATG | T,M 1503 | XP_011540150.1 | |
XM_011541849.2 | 4931 | Missense Mutation | ACG,ATG | T,M 1491 | XP_011540151.1 | |
XM_011541858.2 | 4931 | Missense Mutation | ACG,ATG | T,M 1200 | XP_011540160.1 | |
XM_017001899.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1503 | XP_016857388.1 | |
XM_017001900.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1502 | XP_016857389.1 | |
XM_017001901.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1503 | XP_016857390.1 | |
XM_017001902.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1502 | XP_016857391.1 | |
XM_017001903.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1480 | XP_016857392.1 | |
XM_017001904.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1470 | XP_016857393.1 | |
XM_017001905.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1469 | XP_016857394.1 | |
XM_017001906.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1470 | XP_016857395.1 | |
XM_017001907.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1448 | XP_016857396.1 | |
XM_017001908.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1448 | XP_016857397.1 | |
XM_017001909.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1448 | XP_016857398.1 | |
XM_017001910.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1415 | XP_016857399.1 | |
XM_017001911.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1415 | XP_016857400.1 | |
XM_017001912.1 | 4931 | Missense Mutation | ACG,ATG | T,M 1393 | XP_016857401.1 |