Product Details

SNP ID

rs34654901

Assay Type

Functionally tested

NCBI dbSNP Submissions

16

Location

Chr.1:159065976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGAGTTTGAAGCGTGTTGATCTT[A/C]GGGGTTTCACCAGCTTTTCTGATAA

Phenotype

MIM: 604578

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

AIM2 PubMed Links

Gene Details

Gene

AIM2

Gene Name

absent in melanoma 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004833.1	995	Silent Mutation			NP_004824.1
XM_005245616.4	995	Silent Mutation			XP_005245673.1
XM_017002848.1	995	Silent Mutation			XP_016858337.1

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