Product Details

SNP ID
rs11121750
Assay Type
Functionally tested
NCBI dbSNP Submissions
37
Location
Chr.1:11482842 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGTCTTCTTCTCTGTCTGCCCTCCC[C/T]CTACCCAAGCATGGTGTCTTGCCAA
Phenotype
MIM: 611251
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
DISP3 PubMed Links

Gene Details

Gene
DISP3
Gene Name
dispatched RND transporter family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020780.1 Intron NP_065831.1
XM_011541828.2 Intron XP_011540130.1
XM_011541829.1 Intron XP_011540131.1
XM_011541830.2 Intron XP_011540132.1
XM_011541831.2 Intron XP_011540133.1
XM_011541832.2 Intron XP_011540134.1
XM_011541833.2 Intron XP_011540135.1
XM_011541835.2 Intron XP_011540137.1

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