Product Details

SNP ID
rs202147120
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:106563777 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCACTGAGCAGATAGCAGAAGACT[C/G]CTGCCTGACGATTGTGGGCAGCCTG
Phenotype
MIM: 601797 MIM: 610502
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
AIM1 PubMed Links

Gene Details

Gene
AIM1
Gene Name
absent in melanoma 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001624.3 5415 Missense Mutation TCC,TGC S1643C NP_001615.2
XM_005266839.3 5415 Missense Mutation TCC,TGC S2051C XP_005266896.1
XM_017010333.1 5415 UTR 3 XP_016865822.1
Gene
RTN4IP1
Gene Name
reticulon 4 interacting protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318746.1 5415 Intron NP_001305675.1
NM_032730.5 5415 Intron NP_116119.2
XM_011536192.2 5415 Intron XP_011534494.1
XM_017011375.1 5415 Intron XP_016866864.1
XM_017011376.1 5415 Intron XP_016866865.1

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