Product Details

SNP ID

rs1196351

Assay Type

Functionally tested

NCBI dbSNP Submissions

65

Location

Chr.1:151627965 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTTCAGACTGGCTTCTTTCCCTT[A/G]GCAACATGGACTTAAGGTTCCTGCA

Phenotype

MIM: 611541

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SNX27 PubMed Links

Gene Details

Gene

SNX27

Gene Name

sorting nexin family member 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030918.5		Intron			NP_112180.4
XM_005245509.2		Intron			XP_005245566.1
XM_005245510.3		Intron			XP_005245567.1
XM_005245511.4		Intron			XP_005245568.1
XM_011510024.2		Intron			XP_011508326.1
XM_011510025.2		Intron			XP_011508327.1
XM_011510026.2		Intron			XP_011508328.1
XM_017002417.1		Intron			XP_016857906.1

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