Product Details

SNP ID

rs149697090

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:153767124 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTAATCGACAGCCCTGACTGCGT[C/G]CCCTTCCGTGACCCAGCCGAGTGCC

Phenotype

MIM: 300214

Polymorphism

C/G, 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	471	Silent Mutation	GTC,GTG	V122V	NP_001156729.1
NM_005393.2	471	Silent Mutation	GTC,GTG	V99V	NP_005384.2

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