Product Details

SNP ID

rs145960363

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:125447811 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCTAAAGCATTCCTTAGCATTGG[C/T]CCAAACTTGAATTCCCTAAAAATAA

Phenotype

MIM: 605931

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SNX4 PubMed Links

Gene Details

Gene

SNX4

Gene Name

sorting nexin 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003794.3	1451	Missense Mutation	ACC,GCC	T441A	NP_003785.1
XM_017007414.1	1451	Missense Mutation	ACC,GCC	T473A	XP_016862903.1

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