Product Details

SNP ID

rs137871765

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:81802443 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCAGAGGACTCCACCTTTAGGATC[C/T]GTTCACCTTCTGTTTCTGACACATC

Phenotype

MIM: 614903

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SNX16 PubMed Links

Gene Details

Gene

SNX16

Gene Name

sorting nexin 16

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022133.3	1136	Missense Mutation	CAG,CGG	Q292R	NP_071416.2
NM_152836.2	1136	Missense Mutation	CAG,CGG	Q292R	NP_690049.1
NM_152837.2	1136	Missense Mutation	CAG,CGG	Q263R	NP_690050.1
XM_005251282.4	1136	Missense Mutation	CAG,CGG	Q263R	XP_005251339.1
XM_005251283.2	1136	Missense Mutation	CAG,CGG	Q263R	XP_005251340.1
XM_011517574.2	1136	Missense Mutation	CAG,CGG	Q135R	XP_011515876.1

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