Hs01761992_cn

• Gene Symbol: FAM98C
• Assay Reference Genome Location: Chr.19:38408828 on build GRCh38
• Cytoband: 19q13.2

Target Gene Details

• Entrez Gene ID: 147965
• Gene Name: family with sequence similarity 98 member C
• Gene Aliases: -
• Location: Chr.19:38403124-38409088 on Build GRCh38
• Assay Gene Location: Within Exon 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM98C	NM_174905.3	8	1015	NP_777565.3
	AK128745.1	5	3880
	BC080606.1	6	713	AAH80606.1
	BC117258.1	8	1015
	BC143830.1	8	1015
	BI871449.1	5	547
	BM561971.1	8	958
	BX641942.1	1	278

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv833822	Chr.19:38270108 - 38454465 on Build GRCh38	Loss	RYR1 FAM98C KCNK6 RASGRP4 SPRED3 C19orf33 GGN CATSPERG SPINT2 PSMD8 YIF1B
nsv833823	Chr.19:38364910 - 38545160 on Build GRCh38	Loss	RYR1 FAM98C RASGRP4 SPRED3 GGN CATSPERG PSMD8
dgv3525n100	Chr.19:38405604 - 38459089 on Build GRCh38	Gain	RYR1 FAM98C RASGRP4
nsv470140	Chr.19:38349499 - 38628854 on Build GRCh38	Gain	RYR1 FAM98C RASGRP4 SPRED3 GGN CATSPERG PSMD8 LOC105372397 MAP4K1 EIF3K
nsv1064275	Chr.19:38369225 - 38422611 on Build GRCh38	Loss	FAM98C RASGRP4 SPRED3 GGN CATSPERG PSMD8

More Information

Additional Information:

For this assay, SNP(s) [rs142977446] are located under a primer or 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.

• Set Membership: Intragenic, Exonic, DGV Variation

Panther Classification:

Molecular Function -

RNA metabolism protein, RNA processing factor, RNA splicing factor, nucleic acid metabolism protein