Product Details

SNP ID
rs7952784
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:108912459 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGAGTTCTTGATGTCGGCAGTGACA[A/G]TCAGTGCCCCAGTTGGGGCCTGCCA
Phenotype
MIM: 611699
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SVOP PubMed Links

Gene Details

Gene
SVOP
Gene Name
SV2 related protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018711.4 2095 UTR 3 NP_061181.1

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