Product Details

SNP ID

rs149711096

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:19216988 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGTTTGTCTGGGCCTTGGGCCTTT[C/T]GATGCTGCAGATGCTGCTCTTTGTG

Phenotype

MIM: 600826

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NCAN PubMed Links

Gene Details

Gene

NCAN

Gene Name

neurocan

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004386.2	134	Missense Mutation	TCG,TTG	S12L	NP_004377.2

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