Product Details

SNP ID

rs143978612

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:23469720 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGGGGTGGGCTTTGCGAAGATGG[C/T]GGCGCTGGTGAGTTTGGTGTGGTTT

Phenotype

MIM: 610777

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NGDN PubMed Links

Gene Details

Gene

NGDN

Gene Name

neuroguidin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042635.1	32	Missense Mutation	GCG,GTG	A2V	NP_001036100.1
NM_015514.1	32	Missense Mutation	GCG,GTG	A2V	NP_056329.1

View Full Product Details