Product Details

SNP ID

rs141245495

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:32768976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACACGATCCTATCAGAGAAAGGTAA[C/G]AGAGAAAAGGTCTTCTATGGCCCTG

Phenotype

MIM: 136535

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FMN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs5811704] 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

FMN1

Gene Name

formin 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001103184.3	8502	UTR 3			NP_001096654.1
NM_001277313.1	8502	UTR 3			NP_001264242.1
NM_001277314.1	8502	Intron			NP_001264243.1
XM_011521504.2	8502	UTR 3			XP_011519806.1
XM_011521505.2	8502	Intron			XP_011519807.1
XM_011521506.2	8502	UTR 3			XP_011519808.1
XM_011521507.2	8502	Intron			XP_011519809.1
XM_011521509.2	8502	UTR 3			XP_011519811.1
XM_011521511.2	8502	UTR 3			XP_011519813.1
XM_017022130.1	8502	UTR 3			XP_016877619.1
XM_017022131.1	8502	Intron			XP_016877620.1
XM_017022132.1	8502	UTR 3			XP_016877621.1
XM_017022133.1	8502	UTR 3			XP_016877622.1
XM_017022134.1	8502	UTR 3			XP_016877623.1
XM_017022135.1	8502	UTR 3			XP_016877624.1

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