Product Details

SNP ID

rs2645992

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:112760281 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTCATTGAGCAGGAGCTGGGACCT[T/C]AGAGGAAGGGGGCCCTGGAGGGGAG

Phenotype

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

SNX30 PubMed Links

Gene Details

Gene

SNX30

Gene Name

sorting nexin family member 30

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012994.1		Intron			NP_001013012.1
XM_011518691.2		Intron			XP_011516993.1
XM_017014716.1		Intron			XP_016870205.1

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