Product Details

SNP ID

rs7767309

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:106366092 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTTCTTCAGAAAAAGAACAATCAT[C/T]TAAAATGTTATTTGAAAGCATTCTG

Phenotype

MIM: 601797

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
XM_005266839.3		Intron			XP_005266896.1
XM_017010333.1		Intron			XP_016865822.1

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