Product Details

SNP ID

rs200875272

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:125453823 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCATCTTTACCTGCCTTCCAGAT[G/T]TTTAGACTTTAGCTGTTGTTCTCCT

Phenotype

MIM: 605931

Polymorphism

G/T, Transversion 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	1307	Missense Mutation	AAT,CAT	N393H	NP_003785.1
XM_017007414.1	1307	Missense Mutation	AAT,CAT	N425H	XP_016862903.1

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