Product Details

SNP ID

rs1902328

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:49632587 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCCAACCCTTCCCCCTCCTCTTT[C/T]TTCGGCAGACGGCTCCGGGTGCGGA

Phenotype

MIM: 616288

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FMNL3 PubMed Links

Additional Information

For this assay, SNP(s) [rs79252534] 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

FMNL3

Gene Name

formin like 3

There are no transcripts associated with this gene.

Gene

PRPF40B

Gene Name

pre-mRNA processing factor 40 homolog B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001031698.2		Intron			NP_001026868.2
NM_012272.2		Intron			NP_036404.1
XM_006719324.3		Intron			XP_006719387.1
XM_006719325.3		Intron			XP_006719388.1
XM_011538135.2		Intron			XP_011536437.1
XM_011538136.2		Intron			XP_011536438.1
XM_011538137.2		Intron			XP_011536439.1
XM_011538138.2		Intron			XP_011536440.1
XM_011538139.2		Intron			XP_011536441.1
XM_011538140.2		Intron			XP_011536442.1
XM_011538141.1		Intron			XP_011536443.1
XM_011538143.2		Intron			XP_011536445.1
XM_011538144.2		Intron			XP_011536446.1
XM_017019135.1		Intron			XP_016874624.1
XM_017019136.1		Intron			XP_016874625.1
XM_017019137.1		Intron			XP_016874626.1
XM_017019138.1		Intron			XP_016874627.1
XM_017019139.1		Intron			XP_016874628.1

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