Product Details

SNP ID
rs4761998
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:51288375 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTCAGAAATCTCACACACTTCTCCC[A/G]GATATACACATGGCTCATGTGCTAG
Phenotype
MIM: 605936
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BIN2 PubMed Links

Gene Details

Gene
BIN2
Gene Name
bridging integrator 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001290007.1 Intron NP_001276936.1
NM_001290008.1 Intron NP_001276937.1
NM_001290009.1 Intron NP_001276938.1
NM_016293.3 Intron NP_057377.3
XM_005268957.3 Intron XP_005269014.2
XM_005268958.3 Intron XP_005269015.1
XM_017019422.1 Intron XP_016874911.1

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