Product Details

SNP ID

rs4883527

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:132498246 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTCGCTCACAGTGAGGCCTGTGT[C/G]GGGGGCATGGGGCCGGGGGCTGTGT

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FBRSL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs188574183] 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

FBRSL1

Gene Name

fibrosin like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142641.1		Intron			NP_001136113.1
XM_005266171.3		Intron			XP_005266228.1
XM_005266173.3		Intron			XP_005266230.1
XM_005266175.3		Intron			XP_005266232.1
XM_005266176.3		Intron			XP_005266233.1
XM_005266177.3		Intron			XP_005266234.1
XM_005266181.3		Intron			XP_005266238.1
XM_011534803.2		Intron			XP_011533105.1
XM_011534804.2		Intron			XP_011533106.1
XM_011534805.2		Intron			XP_011533107.1
XM_011534806.2		Intron			XP_011533108.1
XM_011534807.2		Intron			XP_011533109.1
XM_011534808.2		Intron			XP_011533110.1
XM_011534809.2		Intron			XP_011533111.1
XM_011534810.2		Intron			XP_011533112.1
XM_011534812.2		Intron			XP_011533114.1
XM_011534816.2		Intron			XP_011533118.1

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