Product Details

SNP ID
rs202085045
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:12942265 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATATAGGCGAGTACATTTACCTGC[A/G]GCTGAATGGGAGTACCATATGAAGT
Phenotype
MIM: 607437
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM234B PubMed Links

Gene Details

Gene
FAM234B
Gene Name
family with sequence similarity 234 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020853.1 3399 Intron NP_065904.1
XM_017019706.1 3399 Intron XP_016875195.1
Gene
GPRC5D
Gene Name
G protein-coupled receptor class C group 5 member D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018654.1 3399 Missense Mutation CCG,CTG P320L NP_061124.1
XM_005253421.3 3399 Missense Mutation CCG,CTG P320L XP_005253478.1
XM_017019582.1 3399 Missense Mutation CCG,CTG P320L XP_016875071.1
XM_017019583.1 3399 Intron XP_016875072.1

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