Product Details

SNP ID
rs199628078
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:77614736 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCGTGGCGCACGTGGGCTGCTGCC[A/G]GTTGAAGTTGAGCCGCCAGCGGCGC
Phenotype
MIM: 609791
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LINGO1 PubMed Links

Gene Details

Gene
LINGO1
Gene Name
leucine rich repeat and Ig domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301186.1 1365 Silent Mutation NP_001288115.1
NM_001301187.1 1365 Silent Mutation NP_001288116.1
NM_001301189.1 1365 Silent Mutation NP_001288118.1
NM_001301191.1 1365 Silent Mutation NP_001288120.1
NM_001301192.1 1365 Silent Mutation NP_001288121.1
NM_001301194.1 1365 Silent Mutation NP_001288123.1
NM_001301195.1 1365 Silent Mutation NP_001288124.1
NM_001301197.1 1365 Silent Mutation NP_001288126.1
NM_001301198.1 1365 Silent Mutation NP_001288127.1
NM_001301199.1 1365 Silent Mutation NP_001288128.1
NM_001301200.1 1365 Silent Mutation NP_001288129.1
NM_032808.6 1365 Silent Mutation NP_116197.4
XM_011522118.2 1365 Missense Mutation XP_011520420.1
XM_017022682.1 1365 Missense Mutation XP_016878171.1

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