Product Details

SNP ID
rs1072778
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.12:31672037 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
ATTTAAGAAACAGAATCCAACACCA[T/C]AGATCAGAGTTCATGCTAGGATTAT
Phenotype
MIM: 615256
Polymorphism
T/C, Transition Substitution
Allele Nomenclature
Literature Links
AMN1 PubMed Links
Additional Information
For this assay, SNP(s) [rs140375565] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
AMN1
Gene Name
antagonist of mitotic exit network 1 homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001113402.1 4503 UTR 3 NP_001106873.1
NM_001278411.1 4503 UTR 3 NP_001265340.1
NM_001278412.1 4503 UTR 3 NP_001265341.1
XM_006719054.3 4503 UTR 3 XP_006719117.1
XM_011520604.2 4503 UTR 3 XP_011518906.1
XM_017018963.1 4503 UTR 3 XP_016874452.1
XM_017018964.1 4503 UTR 3 XP_016874453.1
XM_017018965.1 4503 UTR 3 XP_016874454.1
Gene
ETFBKMT
Gene Name
electron transfer flavoprotein beta subunit lysine methyltransferase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135863.1 4503 Intron NP_001129335.1
NM_001135864.1 4503 Intron NP_001129336.1
NM_173802.3 4503 Intron NP_776163.1

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