Product Details

SNP ID
rs1127100
Assay Type
Functionally tested
NCBI dbSNP Submissions
47
Location
Chr.1:31728046 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCACGGTGCACACGCTCCGCTCGGC[C/T]GCCCCACCCGAGGACACACTCCACC
Phenotype
MIM: 602683
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ADGRB2 PubMed Links

Gene Details

Gene
ADGRB2
Gene Name
adhesion G protein-coupled receptor B2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001294335.1 4974 Silent Mutation GCA,GCG A1516A NP_001281264.1
NM_001294336.1 4974 Silent Mutation GCA,GCG A1483A NP_001281265.1
XM_011541848.2 4974 Silent Mutation GCA,GCG A1517A XP_011540150.1
XM_011541849.2 4974 Silent Mutation GCA,GCG A1505A XP_011540151.1
XM_011541858.2 4974 Silent Mutation GCA,GCG A1214A XP_011540160.1
XM_017001899.1 4974 Silent Mutation GCA,GCG A1517A XP_016857388.1
XM_017001900.1 4974 Silent Mutation GCA,GCG A1516A XP_016857389.1
XM_017001901.1 4974 Intron XP_016857390.1
XM_017001902.1 4974 Intron XP_016857391.1
XM_017001903.1 4974 Silent Mutation GCA,GCG A1494A XP_016857392.1
XM_017001904.1 4974 Silent Mutation GCA,GCG A1484A XP_016857393.1
XM_017001905.1 4974 Silent Mutation GCA,GCG A1483A XP_016857394.1
XM_017001906.1 4974 Intron XP_016857395.1
XM_017001907.1 4974 Silent Mutation GCA,GCG A1462A XP_016857396.1
XM_017001908.1 4974 Silent Mutation GCA,GCG A1462A XP_016857397.1
XM_017001909.1 4974 Intron XP_016857398.1
XM_017001910.1 4974 Silent Mutation GCA,GCG A1429A XP_016857399.1
XM_017001911.1 4974 Intron XP_016857400.1
XM_017001912.1 4974 Silent Mutation GCA,GCG A1407A XP_016857401.1

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