Genomic Map
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Target Gene Details
Entrez Gene ID: | 1572 |
Gene Name: | cytochrome P450 family 2 subfamily F member 1 |
Gene Aliases: |
C2F1, CYP2F, CYPIIF1 |
Location: |
Chr.19:41114292-41128381 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CYP2F1 | NM_000774.4 | NP_000765.2 | ||
| NR_135528.1 | ||||
| XM_011526551.2 | XP_011524853.1 | |||
| XM_011526552.2 | XP_011524854.1 | |||
| XM_011526553.2 | XP_011524855.1 | |||
| XM_011526554.2 | XP_011524856.1 | |||
| XM_011526555.2 | XP_011524857.1 | |||
| XM_017026384.1 | XP_016881873.1 | |||
| XM_017026385.1 | XP_016881874.1 | |||
| XM_017026387.1 | XP_016881876.1 | |||
| AK298082.1 | ||||
| AK316498.1 | ||||
| BC109056.1 | AAI09057.1 | |||
| CB853363.1 | ||||
| J02906.1 | AAA52156.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv2492 | Chr.19:41096554 - 41131195 on Build GRCh38 | Insertion |
 CYP2F1
|
| esv3644372 | Chr.19:41119456 - 41147784 on Build GRCh38 | Gain |
CYP2F1
|
| nsv1065684 | Chr.19:41010484 - 41138637 on Build GRCh38 | Gain |
CYP2F1
CYP2A7P1
CYP2B6
CYP2A13
|
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Additional Information:
For this assay, SNP(s) [rs73545059] 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
|
Panther Classification:
Gene Ontology Categories:
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