Product Details

SNP ID

rs150225142

Assay Type

Functionally Tested

NCBI dbSNP Submissions

14

Location

Chr.1:37997805 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCTGCCAGGGGCGTCTGGCATCC[A/G]GTACAGACCAGACATTCTCGATGCC

Phenotype

MIM: 602790 MIM: 605596

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FHL3 PubMed Links

Additional Information

For this assay, SNP(s) [rs7366048] 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

FHL3

Gene Name

four and a half LIM domains 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243878.1	170	Silent Mutation	ACC,ACT	T81T	NP_001230807.1
NM_004468.4	170	Silent Mutation	ACC,ACT	T189T	NP_004459.2
XM_017000675.1	170	Silent Mutation	ACC,ACT	T56T	XP_016856164.1

Gene

SF3A3

Gene Name

splicing factor 3a subunit 3

There are no transcripts associated with this gene.

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