Product Details

SNP ID
rs4396961
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:89242466 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGGTTGCAGCTGTCTTGAGTTTTAA[A/G]CCAGCAAGACTTTGAGTGGCTCCTC
Phenotype
MIM: 611241
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GPRIN3 PubMed Links

Gene Details

Gene
GPRIN3
Gene Name
GPRIN family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_198281.2 7962 Intron NP_938022.2
XM_005262936.3 7962 UTR 3 XP_005262993.1
XM_005262937.4 7962 UTR 3 XP_005262994.1
XM_017008043.1 7962 UTR 3 XP_016863532.1
XM_017008044.1 7962 UTR 3 XP_016863533.1

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