Product Details

SNP ID
rs12326723
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:24430260 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAAAAAATTTATTTGTGATGTAATC[A/T]GTAATTTGAGGTATAAACATAATCC
Phenotype
MIM: 615319
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
IMPACT PubMed Links

Gene Details

Gene
IMPACT
Gene Name
impact RWD domain protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018439.3 Intron NP_060909.1
XM_017025832.1 Intron XP_016881321.1

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