Product Details

SNP ID

rs10145029

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:34575559 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAAGTATAATAAAGAGGAAACTTT[C/T]ATGTAGGGTTTCCCACATGAAATAT

Phenotype

MIM: 606098

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SNX6 PubMed Links

Gene Details

Gene

SNX6

Gene Name

sorting nexin 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021249.3		Intron			NP_067072.3
NM_152233.2		Intron			NP_689419.2
XM_006720224.1		Intron			XP_006720287.1

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