Product Details

SNP ID

rs199976207

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:77614934 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGCGGAAGGCATAGGGCTCCACCA[C/T]GGCCAGCTGCCCGCCCACCAGCTGG

Phenotype

MIM: 609791

Polymorphism

C/T, 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	1167	Missense Mutation	ATG,GTG	M319V	NP_001288115.1
NM_001301187.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288116.1
NM_001301189.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288118.1
NM_001301191.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288120.1
NM_001301192.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288121.1
NM_001301194.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288123.1
NM_001301195.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288124.1
NM_001301197.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288126.1
NM_001301198.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288127.1
NM_001301199.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288128.1
NM_001301200.1	1167	Missense Mutation	ATG,GTG	M319V	NP_001288129.1
NM_032808.6	1167	Missense Mutation	ATG,GTG	M325V	NP_116197.4
XM_011522118.2	1167	Missense Mutation	ATG,GTG	M319V	XP_011520420.1
XM_017022682.1	1167	Missense Mutation	ATG,GTG	M319V	XP_016878171.1

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