Product Details

SNP ID

rs143690947

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:153765537 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTGGGGCAGCTGAACTGAGCGTA[G/T]GTGCCACGCCGCCCAGGAGACCCCT

Phenotype

MIM: 300214

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

PLXNB3 PubMed Links

Gene Details

Gene

PLXNB3

Gene Name

plexin B3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163257.1	176	UTR 5			NP_001156729.1
NM_005393.2	176	Missense Mutation	AGG,ATG	R1M	NP_005384.2

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