Product Details

SNP ID

rs200363020

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:64096095 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCCTGGAGCCGGAGTCCGAGGGG[A/G]CGGCCGGGGGATCAGAACCCGAGGC

Phenotype

MIM: 601272

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM96A PubMed Links

Gene Details

Gene

FAM96A

Gene Name

family with sequence similarity 96 member A

There are no transcripts associated with this gene.

Gene

SNX1

Gene Name

sorting nexin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242933.1	212	Missense Mutation	ACG,GCG	T28A	NP_001229862.1
NM_003099.4	212	Missense Mutation	ACG,GCG	T28A	NP_003090.2
NM_148955.3	212	Missense Mutation	ACG,GCG	T28A	NP_683758.1
XM_005254611.2	212	Intron			XP_005254668.1

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