Genomic Map
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Target Gene Details
Entrez Gene ID: | 729830 |
Gene Name: | family with sequence similarity 160 member A1 |
Gene Aliases: |
- |
Location: |
Chr.4:151409143-151670503 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM160A1 | NM_001109977.1 | NP_001103447.1 | ||
| XM_005263199.1 | XP_005263256.1 | |||
| XM_011532221.2 | XP_011530523.1 | |||
| XM_011532222.2 | XP_011530524.1 | |||
| XM_011532223.2 | XP_011530525.1 | |||
| DA722299.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1028814 | Chr.4:150874356 - 152285445 on Build GRCh38 | Gain |
 LOC100505685
LOC100996286
RPS3A
GATB
SNORD73A
SH3D19
PRSS48
FAM160A1
LRBA
|
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Additional Information:
For this assay, SNP(s) [rs74928203] 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
Intronic
Non-exonic
DGV Variation
|
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