Product Details

SNP ID

rs150443540

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:2858923 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGGAGCCTTTGCGGTGATTCAAG[C/G]GGGGGAGCACTTTGCAAGGGAGTGG

Phenotype

MIM: 602341

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FOXM1 PubMed Links

Additional Information

For this assay, SNP(s) [rs28919869] are located under a probe 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

FOXM1

Gene Name

forkhead box M1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243088.1	2290	Silent Mutation	CCC,CCG	P654P	NP_001230017.1
NM_001243089.1	2290	Silent Mutation	CCC,CCG	P653P	NP_001230018.1
NM_021953.3	2290	Silent Mutation	CCC,CCG	P669P	NP_068772.2
NM_202002.2	2290	Silent Mutation	CCC,CCG	P707P	NP_973731.1
NM_202003.2	2290	Silent Mutation	CCC,CCG	P654P	NP_973732.1
XM_005253676.3	2290	Silent Mutation	CCC,CCG	P670P	XP_005253733.1
XM_011520930.2	2290	Silent Mutation	CCC,CCG	P669P	XP_011519232.1
XM_011520931.2	2290	Silent Mutation	CCC,CCG	P655P	XP_011519233.1
XM_011520932.1	2290	Intron			XP_011519234.1
XM_011520933.1	2290	Intron			XP_011519235.1
XM_011520934.2	2290	UTR 3			XP_011519236.1
XM_011520935.1	2290	Intron			XP_011519237.1

Gene

LOC100507424

Gene Name

uncharacterized LOC100507424

There are no transcripts associated with this gene.

Gene

LOC101929469

Gene Name

uncharacterized protein ENSP00000372125

There are no transcripts associated with this gene.

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