Product Details

SNP ID

rs8066391

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:48117934 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGGCTGATGCAGGAGGATTACTT[C/G]ATCCCAGGAATTTGAGGCTGCGGCG

Phenotype

MIM: 614906

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SNX11 PubMed Links

Gene Details

Gene

SNX11

Gene Name

sorting nexin 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013323.2		Intron			NP_037455.2
NM_152244.1		Intron			NP_689450.1
XM_005257260.3		Intron			XP_005257317.1
XM_005257261.3		Intron			XP_005257318.1
XM_005257262.3		Intron			XP_005257319.1
XM_011524697.2		Intron			XP_011522999.1

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