Product Details

SNP ID

rs201322412

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:17794179 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGGAAATAAGGTTTCTAAAAAGC[C/T]TTCCAAGAAGACATAAACCATTCTC

Phenotype

MIM: 606589

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SNX13 PubMed Links

Gene Details

Gene

SNX13

Gene Name

sorting nexin 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015132.4	2884	Missense Mutation	AGC,GGC	S914G	NP_055947.1
XM_005249672.1	2884	Missense Mutation	AGC,GGC	S925G	XP_005249729.1
XM_005249673.4	2884	Intron			XP_005249730.1
XM_011515229.1	2884	Missense Mutation	AGC,GGC	S871G	XP_011513531.1
XM_011515230.2	2884	Missense Mutation	AGC,GGC	S845G	XP_011513532.1
XM_011515231.2	2884	Missense Mutation	AGC,GGC	S845G	XP_011513533.1
XM_011515233.2	2884	Missense Mutation	AGC,GGC	S823G	XP_011513535.1
XM_017011893.1	2884	Missense Mutation	AGC,GGC	S860G	XP_016867382.1
XM_017011894.1	2884	Missense Mutation	AGC,GGC	S845G	XP_016867383.1
XM_017011895.1	2884	Missense Mutation	AGC,GGC	S812G	XP_016867384.1
XM_017011896.1	2884	Missense Mutation	AGC,GGC	S796G	XP_016867385.1
XM_017011897.1	2884	Missense Mutation	AGC,GGC	S962G	XP_016867386.1

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