Product Details

SNP ID
rs140656810
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:64096048 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGGTGGTGGCTGTAGCGCTTCGG[A/G]GAGACTGCCTCCGCCCTTCCCCGGC
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_001242933.1 165 Missense Mutation GAG,GGG E12G NP_001229862.1
NM_003099.4 165 Missense Mutation GAG,GGG E12G NP_003090.2
NM_148955.3 165 Missense Mutation GAG,GGG E12G NP_683758.1
XM_005254611.2 165 Intron XP_005254668.1

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