Product Details

SNP ID
rs2383749
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:27937914 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GATTATCATGAAATGAGGAGAATTA[C/T]AGCTTCTCTTCCAATAAAGGAGAAA
Phenotype
MIM: 609793
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LINGO2 PubMed Links

Gene Details

Gene
LINGO2
Gene Name
leucine rich repeat and Ig domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001258282.1 17179 Intron NP_001245211.1
NM_152570.2 17179 Intron NP_689783.1
XM_011517719.1 17179 UTR 3 XP_011516021.1
XM_011517724.2 17179 UTR 3 XP_011516026.1
XM_011517728.2 17179 UTR 3 XP_011516030.1
XM_017014303.1 17179 UTR 3 XP_016869792.1
XM_017014304.1 17179 UTR 3 XP_016869793.1
XM_017014305.1 17179 UTR 3 XP_016869794.1
XM_017014306.1 17179 UTR 3 XP_016869795.1
XM_017014307.1 17179 UTR 3 XP_016869796.1

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