TIPARP
TCDD inducible poly(ADP-ribose) polymerase
Summary
This gene encodes a member of the poly(ADP-ribose) polymerase superfamily. Studies of the mouse ortholog have shown that the encoded protein catalyzes histone poly(ADP-ribosyl)ation and may be involved in T-cell function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs765576832 | 3:156,395,548 | A/G | — | uncertain significance |
| rs1346761723 | 3:156,395,664 | T/A | — | uncertain significance |
| rs2473540288 | 3:156,395,776 | A/G | — | uncertain significance |
| rs747722067 | 3:156,395,841 | G/A | — | uncertain significance |
| rs2473540564 | 3:156,395,857 | C/T | — | uncertain significance |
| rs757036019 | 3:156,395,862 | C/T | — | uncertain significance |
| rs558453273 | 3:156,395,892 | C/T | — | uncertain significance |
| rs746258116 | 3:156,395,953 | C/T | — | uncertain significance |
| rs772403493 | 3:156,395,959 | A/G | — | uncertain significance |
| rs776070977 | 3:156,395,973 | C/G | — | uncertain significance |
| rs372015234 | 3:156,396,025 | A/G | — | uncertain significance |
| rs201843889 | 3:156,396,123 | G/A | — | uncertain significance |
| rs758347957 | 3:156,396,159 | G/C | — | uncertain significance |
| rs779765422 | 3:156,396,252 | G/T | — | uncertain significance |
| rs748156388 | 3:156,396,300 | A/G | — | uncertain significance |
| rs145662613 | 3:156,396,334 | A/G | — | uncertain significance |
| rs2665390 | 3:156,397,749 | C/A | — | — |
| rs7651446 | 3:156,406,997 | G/T | intron variant | — |
| rs201812887 | 3:156,411,804 | T/C | — | benign |
| rs2473563109 | 3:156,411,865 | T/C | — | uncertain significance |
| rs770403066 | 3:156,411,872 | A/C | — | uncertain significance |
| rs200119519 | 3:156,411,927 | G/C | — | uncertain significance |
| rs2473565755 | 3:156,413,754 | G/A | — | uncertain significance |
| rs184863885 | 3:156,421,482 | A/G | — | uncertain significance |
| rs145937401 | 3:156,422,513 | A/C | — | benign |
| rs766769030 | 3:156,422,618 | A/G | — | uncertain significance |
| rs2473577026 | 3:156,422,721 | T/C | — | uncertain significance |
| rs771313745 | 3:156,422,738 | A/C | — | uncertain significance |
| rs746816452 | 3:156,422,739 | T/C | — | uncertain significance |
| rs761369679 | 3:156,422,747 | C/T | — | uncertain significance |
| rs2473577450 | 3:156,422,813 | G/A | — | uncertain significance |
| rs138664121 | 3:156,422,912 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.