Product Details

SNP ID
rs9486398
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:106564711 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCACTGATAGTCATTTAAAAATAAC[A/G]TAAGAATGACCTAACCTCTGTGTGG
Phenotype
MIM: 601797 MIM: 610502
Polymorphism
A/G, Transition 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 Intron NP_001615.2
XM_005266839.3 Intron XP_005266896.1
XM_017010333.1 Intron 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 Intron NP_001305675.1
NM_032730.5 Intron NP_116119.2
XM_011536192.2 Intron XP_011534494.1
XM_017011375.1 Intron XP_016866864.1
XM_017011376.1 Intron XP_016866865.1

View Full Product Details