Product Details

SNP ID

rs34419602

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:159065931 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTACCTTCTGGACTACAAACAAACC[A/G]TTCACAATTGTTCCAAGGGGCTGAG

Phenotype

MIM: 604578

Polymorphism

A/G, Transition 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	1040	Silent Mutation	AAC,AAT	N265N	NP_004824.1
XM_005245616.4	1040	Silent Mutation	AAC,AAT	N160N	XP_005245673.1
XM_017002848.1	1040	Silent Mutation	AAC,AAT	N265N	XP_016858337.1

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