INPP5F
inositol polyphosphate-5-phosphatase F
Summary
The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase and contains a Sac domain. The activity of this protein is specific for phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol 3,4,5-trisphosphate. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3758618 | 10:121,485,247 | A/T | regulatory region variant | — |
| rs1028755194 | 10:121,485,788 | A/G | — | uncertain significance |
| rs1396133089 | 10:121,485,861 | G/T | — | uncertain significance |
| rs171907 | 10:121,527,997 | C/A | coding sequence variant | — |
| rs772488383 | 10:121,551,078 | C/T | — | uncertain significance |
| rs376893567 | 10:121,551,113 | T/C | — | uncertain significance |
| rs903287908 | 10:121,551,117 | C/T | — | uncertain significance |
| rs1343230533 | 10:121,551,135 | T/A | — | uncertain significance |
| rs772024235 | 10:121,551,528 | G/A | — | uncertain significance |
| rs761223167 | 10:121,556,354 | C/T | — | uncertain significance |
| rs2493301385 | 10:121,557,013 | T/G | — | uncertain significance |
| rs141370318 | 10:121,558,073 | C/T | — | uncertain significance |
| rs562978775 | 10:121,563,709 | G/T | — | uncertain significance |
| rs141464998 | 10:121,564,904 | T/C | — | uncertain significance |
| rs764480287 | 10:121,564,928 | T/C | — | uncertain significance |
| rs202230159 | 10:121,565,951 | G/A | — | uncertain significance |
| rs374196186 | 10:121,565,970 | C/T | — | uncertain significance |
| rs775809247 | 10:121,569,694 | A/G | — | uncertain significance |
| rs2493355667 | 10:121,569,711 | T/C | — | uncertain significance |
| rs763380058 | 10:121,571,338 | C/A | — | uncertain significance |
| rs1851048134 | 10:121,571,383 | A/C | — | uncertain significance |
| rs762311100 | 10:121,580,389 | G/A | — | uncertain significance |
| rs368841218 | 10:121,580,413 | G/T | — | uncertain significance |
| rs769817904 | 10:121,582,699 | G/C | — | uncertain significance |
| rs776547840 | 10:121,583,366 | A/G | — | uncertain significance |
| rs1851660681 | 10:121,583,374 | A/G | — | uncertain significance |
| rs374612807 | 10:121,583,392 | A/G | — | uncertain significance |
| rs752064906 | 10:121,583,397 | T/G | — | uncertain significance |
| rs371493074 | 10:121,586,215 | G/T | — | uncertain significance |
| rs761144165 | 10:121,586,295 | G/A | — | uncertain significance |
| rs1414476657 | 10:121,586,318 | C/A | — | uncertain significance |
| rs771179580 | 10:121,586,322 | A/C | — | uncertain significance |
| rs780096183 | 10:121,586,370 | A/G | — | uncertain significance |
| rs768499612 | 10:121,586,387 | G/C | — | uncertain significance |
| rs747816450 | 10:121,586,409 | T/C | — | uncertain significance |
| rs60994998 | 10:121,586,426 | G/C | — | uncertain significance |
| rs1287690887 | 10:121,586,592 | G/A | — | uncertain significance |
| rs770307046 | 10:121,586,630 | A/G | — | uncertain significance |
| rs548022613 | 10:121,586,635 | C/G | — | uncertain significance |
| rs763341953 | 10:121,586,645 | C/T | — | uncertain significance |
| rs774385559 | 10:121,586,660 | G/T | — | uncertain significance |
| rs752647775 | 10:121,586,717 | T/C | — | uncertain significance |
| rs752592739 | 10:121,586,774 | C/A | — | uncertain significance |
| rs768849313 | 10:121,586,871 | A/G | — | likely benign |
| rs3188055 | 10:121,586,882 | G/A | — | benign |
| rs754544990 | 10:121,586,928 | C/T | — | uncertain significance |
| rs150134182 | 10:121,586,939 | G/T | — | uncertain significance |
| rs761684832 | 10:121,586,975 | G/T | — | uncertain significance |
| rs757621024 | 10:121,587,032 | C/G | — | uncertain significance |
| rs61757087 | 10:121,587,043 | G/C | missense variant | — |
| rs369842188 | 10:121,587,047 | G/A | — | uncertain significance |
| rs1380320459 | 10:121,587,054 | A/G | — | uncertain significance |
| rs148162878 | 10:121,587,065 | T/C | — | uncertain significance |
| rs749321602 | 10:121,587,117 | G/A | — | uncertain significance |
| rs142758118 | 10:121,587,237 | A/C | — | uncertain significance |
| rs1014429108 | 10:121,587,287 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.