Product Details

SNP ID
hCV25750504
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:106561575 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCATCCTTTCATATGCTTTTGAT[C/T]TTTTCTTCAAGTAGATGCAATTTCA
Phenotype
MIM: 601797 MIM: 610502
Polymorphism
C/T, 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
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

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