Product Details

SNP ID

rs989767

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:19817007 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGATCCGCAGCGTTTGGCCCGGTCG[C/T]GCCTATTGCATCGGGAGCCCCCGAG

Phenotype

MIM: 606827

Polymorphism

C/T, 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	793	UTR 5			NP_001269665.1
NM_032812.8	793	UTR 5			NP_116201.7
XM_011519750.2	793	UTR 5			XP_011518052.1

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