Genomic Map
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Target Gene Details
Entrez Gene ID: | 6599 |
Gene Name: | SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1 |
Gene Aliases: |
BAF155, CRACC1, Rsc8, SRG3, SWI3 |
Location: |
Chr.3:47585888-47781915 on Build GRCh38 |
Assay Gene Location: | Within Intron 27 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SMARCC1 | NM_003074.3 | NP_003065.3 | ||
| XM_011534034.1 | XP_011532336.1 | |||
| AK302412.1 | ||||
| AK302541.1 | ||||
| BC050564.1 | AAH50564.1 | |||
| BC113465.1 | ||||
| BC117213.1 | ||||
| U66615.1 | AAC50693.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv3807 | Chr.3:47558395 - 47607814 on Build GRCh38 | Insertion |
 SMARCC1
CSPG5
|
| nsv428417 | Chr.3:46638962 - 47778557 on Build GRCh38 | Loss |
MYL3
ALS2CL
KLHL18
PRSS46
CCDC12
PRSS50
SNORD13P3
PTPN23
CSPG5
PRSS42
SCAP
PRSS43
PRSS45
PTH1R
TMIE
NRADDP
SMARCC1
KIF9
SETD2
ELP6
KIF9-AS1
NBEAL2
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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