Product Details

SNP ID

rs146585589

Assay Type

Functionally Tested

NCBI dbSNP Submissions

17

Location

Chr.1:29148796 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACTCTTGCTGCGGCTGCGACTGC[A/G]ACTGCGGCTCTCCTCTCTGCTTCTC

Phenotype

MIM: 601940

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SRSF4 PubMed Links

Additional Information

For this assay, SNP(s) [rs2230678] 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

SRSF4

Gene Name

serine and arginine rich splicing factor 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005626.4	1182	Missense Mutation	CGC,TGC	R367C	NP_005617.2
XM_011541951.2	1182	Missense Mutation	CGC,TGC	R337C	XP_011540253.1

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