Product Details

SNP ID

rs201234536

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:64096059 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTAGCGCTTCGGAGAGACTGCCT[C/T]CGCCCTTCCCCGGCCTGGAGCCGGA

Phenotype

MIM: 601272

Polymorphism

C/T, 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	176	Missense Mutation	CCG,TCG	P16S	NP_001229862.1
NM_003099.4	176	Missense Mutation	CCG,TCG	P16S	NP_003090.2
NM_148955.3	176	Missense Mutation	CCG,TCG	P16S	NP_683758.1
XM_005254611.2	176	Intron			XP_005254668.1

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