Product Details

SNP ID

rs200340957

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:38405576 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATCAGTACCGCTGCCGCCGCTGC[C/T]TCCTCCTCAAGCGCCTTGACCTCAC

Phenotype

MIM: 607320 MIM: 609293

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM98C PubMed Links

Additional Information

For this assay, SNP(s) [rs3745962] 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

FAM98C

Gene Name

family with sequence similarity 98 member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_174905.3	710	Missense Mutation	CTC,TTC	L231F	NP_777565.3
XM_017026354.1	710	UTR 3			XP_016881843.1

Gene

RASGRP4

Gene Name

RAS guanyl releasing protein 4

There are no transcripts associated with this gene.

Gene

SPRED3

Gene Name

sprouty related EVH1 domain containing 3

There are no transcripts associated with this gene.

View Full Product Details