TPTE2
transmembrane phosphoinositide 3-phosphatase and tensin homolog 2
Summary
TPIP is a member of a large class of membrane-associated phosphatases with substrate specificity for the 3-position phosphate of inositol phospholipids.[supplied by OMIM, Jul 2002]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1190975831 | 13:19,997,304 | C/G | — | uncertain significance |
| rs755930755 | 13:19,999,141 | T/C | — | uncertain significance |
| rs2500370195 | 13:20,000,602 | G/A | — | uncertain significance |
| rs368482243 | 13:20,004,612 | C/T | — | uncertain significance |
| rs373125302 | 13:20,004,649 | T/C | — | uncertain significance |
| rs140778301 | 13:20,006,615 | C/G | — | uncertain significance |
| rs764470955 | 13:20,006,673 | A/G | — | uncertain significance |
| rs748375830 | 13:20,010,408 | T/G | — | uncertain significance |
| rs373033596 | 13:20,010,412 | T/C | — | uncertain significance |
| rs142924803 | 13:20,012,285 | C/T | — | uncertain significance |
| rs764453510 | 13:20,024,300 | T/C | — | uncertain significance |
| rs1878096198 | 13:20,024,446 | C/T | — | uncertain significance |
| rs564469345 | 13:20,024,466 | G/T | — | uncertain significance |
| rs201186141 | 13:20,025,353 | A/C | — | uncertain significance |
| rs770883576 | 13:20,025,355 | C/T | — | uncertain significance |
| rs745435268 | 13:20,025,356 | G/A | — | uncertain significance |
| rs759035513 | 13:20,038,601 | T/C | — | uncertain significance |
| rs1424169262 | 13:20,038,637 | G/A | — | uncertain significance |
| rs148045725 | 13:20,038,658 | G/A | — | uncertain significance |
| rs748366957 | 13:20,039,433 | G/T | — | likely benign |
| rs775410599 | 13:20,039,445 | T/C | — | uncertain significance |
| rs753244046 | 13:20,039,684 | A/G | — | likely benign |
| rs377131026 | 13:20,041,398 | A/C | — | uncertain significance |
| rs775828257 | 13:20,041,455 | T/A | — | uncertain significance |
| rs533323981 | 13:20,048,069 | C/T | — | uncertain significance |
| rs770030606 | 13:20,048,070 | G/C | — | uncertain significance |
| rs201242841 | 13:20,048,099 | C/A | — | uncertain significance |
| rs773288015 | 13:20,048,115 | T/G | — | uncertain significance |
| rs368683219 | 13:20,048,166 | C/T | — | uncertain significance |
| rs1879795681 | 13:20,048,213 | A/G | — | uncertain significance |
| rs2500586658 | 13:20,049,719 | G/A | — | uncertain significance |
| rs2500586680 | 13:20,049,725 | G/T | — | uncertain significance |
| rs748652684 | 13:20,049,761 | C/T | — | uncertain significance |
| rs747924193 | 13:20,056,667 | T/C | — | likely benign |
| rs150048756 | 13:20,091,685 | G/A | intron variant | — |
| rs2880301 | 13:20,100,534 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.