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SNP ID: rs114465109
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:31673588 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAACCATGACAAAGCTGGGTGGCTA[T/C]AGAAGAAGGGGGAAACACTTTCCAA
Phenotype: MIM: 615256
Polymorphism: T/C, Transition substitution
Allele Nomenclature
Literature Links: AMN1 PubMed Links

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		Intron			NP_001106873.1
NM_001278411.1		Intron			NP_001265340.1
NM_001278412.1		Intron			NP_001265341.1
XM_006719054.3		Intron			XP_006719117.1
XM_011520604.2		Intron			XP_011518906.1
XM_017018963.1		Intron			XP_016874452.1
XM_017018964.1		Intron			XP_016874453.1
XM_017018965.1		Intron			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		Intron			NP_001129335.1
NM_001135864.1		Intron			NP_001129336.1
NM_173802.3		Intron			NP_776163.1

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