CSPG4
chondroitin sulfate proteoglycan 4
Summary
A human melanoma-associated chondroitin sulfate proteoglycan plays a role in stabilizing cell-substratum interactions during early events of melanoma cell spreading on endothelial basement membranes. CSPG4 represents an integral membrane chondroitin sulfate proteoglycan expressed by human malignant melanoma cells. [provided by RefSeq, Jul 2008]
Known Variants189 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2505066359 | 15:75,967,899 | A/G | — | uncertain significance |
| rs186191601 | 15:75,967,934 | C/T | — | uncertain significance |
| rs749101671 | 15:75,968,025 | C/T | — | uncertain significance |
| rs772175577 | 15:75,968,043 | C/T | — | uncertain significance |
| rs545688154 | 15:75,968,061 | C/G | — | uncertain significance |
| rs113030903 | 15:75,968,078 | G/T | — | conflicting classifications of pathogenicity |
| rs200662034 | 15:75,968,238 | C/T | — | likely benign |
| rs1291027438 | 15:75,968,313 | G/A | — | uncertain significance |
| rs370893364 | 15:75,968,322 | C/T | — | uncertain significance |
| rs529632713 | 15:75,968,345 | C/T | — | uncertain significance |
| rs148844244 | 15:75,968,355 | G/A | — | uncertain significance |
| rs767875801 | 15:75,968,409 | C/T | — | uncertain significance |
| rs1451304098 | 15:75,968,457 | G/A | — | uncertain significance |
| rs772471893 | 15:75,968,489 | C/G | — | uncertain significance |
| rs775083201 | 15:75,968,531 | A/G | — | uncertain significance |
| rs757001593 | 15:75,968,574 | G/A | — | uncertain significance |
| rs759626664 | 15:75,968,627 | C/T | — | uncertain significance |
| rs545951572 | 15:75,968,633 | C/T | — | uncertain significance |
| rs117177957 | 15:75,968,921 | C/T | — | likely benign |
| rs201971922 | 15:75,968,960 | C/T | — | likely benign |
| rs749581446 | 15:75,968,987 | C/T | — | uncertain significance |
| rs368180303 | 15:75,969,141 | C/T | — | uncertain significance |
| rs368259295 | 15:75,969,153 | G/A | — | uncertain significance |
| rs777921699 | 15:75,969,185 | G/C | — | uncertain significance |
| rs2505068896 | 15:75,969,195 | C/G | — | uncertain significance |
| rs375945014 | 15:75,969,214 | G/A | — | likely benign |
| rs759243000 | 15:75,969,236 | G/T | — | uncertain significance |
| rs1018531916 | 15:75,969,314 | G/A | — | uncertain significance |
| rs535393724 | 15:75,969,326 | C/T | — | uncertain significance |
| rs572700996 | 15:75,969,426 | C/T | — | uncertain significance |
| rs373710408 | 15:75,969,492 | C/T | — | uncertain significance |
| rs2505069607 | 15:75,969,513 | G/T | — | uncertain significance |
| rs745751249 | 15:75,969,570 | C/T | — | uncertain significance |
| rs150717520 | 15:75,969,579 | A/G | — | likely benign |
| rs1330725231 | 15:75,969,588 | C/T | — | uncertain significance |
| rs774706021 | 15:75,969,590 | C/T | — | uncertain significance |
| rs149893313 | 15:75,969,642 | G/T | — | uncertain significance |
| rs764884311 | 15:75,969,687 | C/T | — | likely benign |
| rs374104538 | 15:75,969,704 | T/C | — | uncertain significance |
| rs138232907 | 15:75,970,127 | C/T | — | uncertain significance |
| rs147939771 | 15:75,970,128 | G/A | — | uncertain significance |
| rs11636280 | 15:75,973,288 | G/T | — | — |
| rs762365316 | 15:75,974,714 | G/A | — | uncertain significance |
| rs143855050 | 15:75,974,722 | C/T | — | likely benign |
| rs754159916 | 15:75,974,753 | C/G | — | uncertain significance |
| rs200695467 | 15:75,974,779 | C/T | — | uncertain significance |
| rs144616541 | 15:75,974,990 | G/A | — | uncertain significance |
| rs764282652 | 15:75,975,007 | G/A | — | likely benign |
| rs199703779 | 15:75,975,055 | C/T | — | uncertain significance |
| rs141642595 | 15:75,975,061 | C/T | — | likely benign |
| rs367996596 | 15:75,975,068 | C/G | — | uncertain significance |
| rs147158109 | 15:75,975,207 | C/T | — | uncertain significance |
| rs371831713 | 15:75,975,254 | C/T | — | likely benign |
| rs201427044 | 15:75,975,372 | C/G | — | uncertain significance |
| rs751733501 | 15:75,975,376 | C/G | — | uncertain significance |
| rs765964520 | 15:75,977,129 | A/G | — | uncertain significance |
| rs200660611 | 15:75,977,186 | A/G | — | uncertain significance |
| rs773869871 | 15:75,977,564 | C/T | — | uncertain significance |
| rs1468759675 | 15:75,977,604 | C/T | — | uncertain significance |
| rs1168435238 | 15:75,977,627 | T/G | — | uncertain significance |
| rs201598296 | 15:75,977,682 | C/T | — | uncertain significance |
| rs375081442 | 15:75,977,705 | G/C | — | uncertain significance |
| rs182540548 | 15:75,977,747 | G/A | — | uncertain significance |
| rs750753426 | 15:75,977,766 | C/T | — | likely benign |
| rs144971271 | 15:75,977,799 | C/T | — | uncertain significance |
| rs758020534 | 15:75,977,861 | C/T | — | uncertain significance |
| rs749480503 | 15:75,977,931 | T/C | — | uncertain significance |
| rs531406813 | 15:75,977,958 | G/A | — | uncertain significance |
| rs532349130 | 15:75,978,009 | C/T | — | uncertain significance |
| rs138097734 | 15:75,979,663 | T/A | — | uncertain significance |
| rs757271371 | 15:75,979,678 | C/T | — | likely benign |
| rs1181849304 | 15:75,979,700 | G/T | — | uncertain significance |
| rs530215569 | 15:75,979,732 | G/A | — | uncertain significance |
| rs1172722806 | 15:75,979,739 | C/T | — | uncertain significance |
| rs368042724 | 15:75,979,763 | C/G | — | uncertain significance |
| rs762901959 | 15:75,979,813 | A/G | — | uncertain significance |
| rs113584322 | 15:75,979,814 | G/T | — | uncertain significance |
| rs1894077761 | 15:75,979,826 | C/G | — | uncertain significance |
| rs2505084503 | 15:75,979,838 | G/T | — | uncertain significance |
| rs2505084528 | 15:75,979,853 | T/C | — | uncertain significance |
| rs754344917 | 15:75,979,858 | G/C | — | uncertain significance |
| rs118021045 | 15:75,979,905 | G/A | — | likely benign |
| rs145300285 | 15:75,979,966 | G/A | — | uncertain significance |
| rs757696259 | 15:75,980,059 | G/A | — | uncertain significance |
| rs758235057 | 15:75,980,081 | C/T | — | uncertain significance |
| rs202135077 | 15:75,980,108 | G/A | — | uncertain significance |
| rs781329655 | 15:75,980,230 | G/T | — | uncertain significance |
| rs201069796 | 15:75,980,247 | G/T | — | uncertain significance |
| rs142273329 | 15:75,980,259 | C/T | — | likely benign |
| rs528055676 | 15:75,980,282 | C/A | — | uncertain significance |
| rs771161140 | 15:75,980,348 | C/T | — | uncertain significance |
| rs766266221 | 15:75,980,395 | C/T | — | uncertain significance |
| rs753645133 | 15:75,980,396 | G/A | — | uncertain significance |
| rs1894096526 | 15:75,980,681 | C/T | — | uncertain significance |
| rs141657014 | 15:75,980,704 | A/C | — | likely benign |
| rs564546835 | 15:75,980,738 | G/T | — | uncertain significance |
| rs201568610 | 15:75,980,768 | G/A | — | uncertain significance |
| rs773983017 | 15:75,980,780 | G/A | — | uncertain significance |
| rs370944450 | 15:75,980,798 | C/T | — | uncertain significance |
| rs149811704 | 15:75,980,839 | C/T | — | uncertain significance |
Showing 100 of 189 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.