Product Details

SNP ID

rs6881831

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:172331477 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTAGGAAGCGTGAGTTGCAAGACGC[C/T]GAAGAATCTCATGTGGCCCAAATAA

Phenotype

MIM: 613293

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SH3PXD2B PubMed Links

Gene Details

Gene

SH3PXD2B

Gene Name

SH3 and PX domains 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017995.2		Intron			NP_001017995.1
NM_001308175.1		Intron			NP_001295104.1
XM_017009351.1		Intron			XP_016864840.1

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