Assay Details
Target Gene Details
Entrez Gene ID: | 55215 |
Gene Name: | Fanconi anemia complementation group I |
Gene Aliases: |
KIAA1794 |
Location: |
Chr.15:89243954-89317132 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FANCI | NM_001113378.1 | NP_001106849.1 | ||
NM_018193.2 | NP_060663.2 | |||
XM_011521756.2 | XP_011520058.1 | |||
XM_011521757.2 | XP_011520059.1 | |||
XM_011521764.2 | XP_011520066.1 | |||
XM_011521767.2 | XP_011520069.1 | |||
AK055176.1 | ||||
BC004277.1 | AAH04277.1 | |||
BC140769.1 | ||||
BC144483.1 | ||||
BM461935.1 | ||||
BU187299.1 | ||||
EF469766.1 | ||||
EF567077.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1038140 | Chr.15:89141274 - 89620108 on Build GRCh38 | Gain | MIR9-3 MIR9-3HG RLBP1 TICRR FANCI LOC105371031 LOC105370962 LINC00928 RHCG MIR6766 ABHD2 POLG |
More Information
Additional Information:
For this assay, SNP(s) [rs114229964] 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 |