Product Details

SNP ID

rs4075613

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:38412459 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTAGGTATTATCCATGGTTCAGC[A/G]ATTGTCTGGGGTGGACATTATCTGG

Phenotype

MIM: 607320

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM98C PubMed Links

Additional Information

For this assay, SNP(s) [rs78834767] 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

There are no transcripts associated with this gene.

Gene

RASGRP4

Gene Name

RAS guanyl releasing protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146202.1		Intron			NP_001139674.1
NM_001146203.1		Intron			NP_001139675.1
NM_001146204.1		Intron			NP_001139676.1
NM_001146205.1		Intron			NP_001139677.1
NM_001146206.1		Intron			NP_001139678.1
NM_001146207.1		Intron			NP_001139679.1
NM_170604.2		Intron			NP_733749.1

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