Product Details

SNP ID

rs199646908

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:2290636 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGTCGCCGCGCACCTCGGCCGGGG[G/T]GGCGCAGGCCGGCAGCCGCCCGTCG

Phenotype

MIM: 609792

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

C19orf35 PubMed Links

Gene Details

Gene

C19orf35

Gene Name

chromosome 19 open reading frame 35

There are no transcripts associated with this gene.

Gene

LINGO3

Gene Name

leucine rich repeat and Ig domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101391.1	1269	Missense Mutation	ACC,CCC	T381P	NP_001094861.1

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