Product Details

SNP ID

rs7762388

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:116885259 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATTCAGCTTTTCACCAGTAAAGTG[A/G]GTATACAATATCTTATAGGATTGTT

Phenotype

MIM: 612659

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RFX6 PubMed Links

Gene Details

Gene

RFX6

Gene Name

regulatory factor X6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173560.3		Intron			NP_775831.2
XM_011535589.1		Intron			XP_011533891.1
XM_017010477.1		Intron			XP_016865966.1

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