Product Details

SNP ID
rs150292075
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:19817146 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATGTTACTTTGCCACTTCTTCACG[C/G]ACCAGTTTCAGTTCGCCGATGGGAA
Phenotype
MIM: 606827
Polymorphism
C/G, Transversion 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_001282736.1 932 Missense Mutation CAC,GAC H23D NP_001269665.1
NM_032812.8 932 Missense Mutation CAC,GAC H23D NP_116201.7
XM_011519750.2 932 Missense Mutation CAC,GAC H23D XP_011518052.1

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