Product Details

SNP ID

rs13477649

Assay Type

Pre Designed

NCBI dbSNP Submissions

NA

Location

Chr.4:36890734 on Build GRCm38

Set Membership

Context Sequence [VIC/FAM]

AATACACTTAATGGAAAACCCCAGA[C/T]TATTTCACAATCTGCTATAGCAAAT

Phenotype

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_001165999.1		Intron			NP_001159471.1
NM_001166000.1		Intron			NP_001159472.1
NM_001166001.1		Intron			NP_001159473.1
NM_175516.4		Intron			NP_780725.2

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