Product Details

SNP ID

rs7901380

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:19827957 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTGGGGAGGTTTTCTTATCACATC[A/G]TCAGACTAACCATACATCTAATTGT

Phenotype

MIM: 606827

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PLXDC2 PubMed Links

Gene Details

Gene

PLXDC2

Gene Name

plexin domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282736.1		Intron			NP_001269665.1
NM_032812.8		Intron			NP_116201.7
XM_011519750.2		Intron			XP_011518052.1

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