NUTM2F
NUT family member 2F
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2538626590 | 9:97,080,761 | G/A | — | uncertain significance |
| rs775569752 | 9:97,080,764 | G/A | — | uncertain significance |
| rs1455290540 | 9:97,080,898 | G/A | — | uncertain significance |
| rs766323644 | 9:97,080,958 | C/A | — | uncertain significance |
| rs199966336 | 9:97,081,013 | C/T | — | uncertain significance |
| rs1489351634 | 9:97,081,047 | G/A | — | likely benign |
| rs546172389 | 9:97,081,091 | C/T | — | uncertain significance |
| rs759466424 | 9:97,081,117 | G/A | — | uncertain significance |
| rs372599108 | 9:97,081,237 | G/A | — | uncertain significance |
| rs369329276 | 9:97,081,247 | G/A | — | uncertain significance |
| rs747765379 | 9:97,081,313 | T/C | — | uncertain significance |
| rs774660632 | 9:97,081,324 | A/G | — | uncertain significance |
| rs2538628028 | 9:97,081,351 | G/A | — | uncertain significance |
| rs1452881411 | 9:97,081,357 | G/A | — | uncertain significance |
| rs555822305 | 9:97,081,474 | C/G | — | uncertain significance |
| rs574038296 | 9:97,081,516 | A/G | — | uncertain significance |
| rs776953246 | 9:97,081,955 | C/A | — | uncertain significance |
| rs763019192 | 9:97,081,962 | T/C | — | uncertain significance |
| rs778563985 | 9:97,081,989 | C/G | — | likely benign |
| rs1208891917 | 9:97,082,527 | A/G | — | uncertain significance |
| rs1486973153 | 9:97,082,581 | T/G | — | uncertain significance |
| rs1405805268 | 9:97,082,599 | C/T | — | uncertain significance |
| rs375706271 | 9:97,082,600 | G/A | — | likely benign |
| rs781603170 | 9:97,082,630 | G/A | — | uncertain significance |
| rs1350641214 | 9:97,082,639 | C/A | — | uncertain significance |
| rs2538630349 | 9:97,082,644 | A/G | — | uncertain significance |
| rs1279994060 | 9:97,082,648 | C/T | — | uncertain significance |
| rs149664723 | 9:97,082,651 | C/T | — | uncertain significance |
| rs2538630466 | 9:97,082,701 | A/T | — | uncertain significance |
| rs778188780 | 9:97,082,716 | G/A | — | uncertain significance |
| rs746060354 | 9:97,082,727 | C/A | — | uncertain significance |
| rs2538630619 | 9:97,082,738 | G/A | — | uncertain significance |
| rs758680240 | 9:97,082,791 | G/T | — | uncertain significance |
| rs200093724 | 9:97,082,803 | G/A | — | uncertain significance |
| rs530499022 | 9:97,083,242 | A/G | — | — |
| rs1465851869 | 9:97,083,396 | G/A | — | uncertain significance |
| rs776152428 | 9:97,083,405 | G/T | — | uncertain significance |
| rs761248571 | 9:97,083,410 | C/T | — | likely benign |
| rs745761749 | 9:97,083,470 | G/A | — | uncertain significance |
| rs773863487 | 9:97,084,486 | T/G | — | uncertain significance |
| rs761896962 | 9:97,084,489 | G/A | — | uncertain significance |
| rs755751887 | 9:97,084,511 | G/A | — | uncertain significance |
| rs200378871 | 9:97,084,525 | G/C | — | uncertain significance |
| rs371026938 | 9:97,084,544 | T/C | — | likely benign |
| rs2538634343 | 9:97,084,564 | T/G | — | uncertain significance |
| rs370496850 | 9:97,084,570 | G/A | — | uncertain significance |
| rs753499614 | 9:97,084,574 | T/C | — | uncertain significance |
| rs935973679 | 9:97,084,588 | C/T | — | uncertain significance |
| rs747394175 | 9:97,084,589 | G/A | — | uncertain significance |
| rs773311528 | 9:97,084,611 | G/C | — | uncertain significance |
| rs781484639 | 9:97,087,646 | C/T | — | uncertain significance |
| rs769684475 | 9:97,087,770 | G/A | — | uncertain significance |
| rs1265625850 | 9:97,087,778 | G/T | — | uncertain significance |
| rs1445398697 | 9:97,087,950 | G/A | — | uncertain significance |
| rs749164552 | 9:97,087,952 | G/A | — | uncertain significance |
| rs1014015043 | 9:97,087,962 | G/T | — | uncertain significance |
| rs762282751 | 9:97,088,001 | C/T | — | uncertain significance |
| rs767682956 | 9:97,088,075 | G/C | — | uncertain significance |
| rs750245035 | 9:97,088,087 | G/C | — | uncertain significance |
| rs368683600 | 9:97,088,156 | G/A | — | uncertain significance |
| rs764213966 | 9:97,088,193 | C/T | — | likely benign |
| rs1052320247 | 9:97,088,195 | C/T | — | uncertain significance |
| rs751365201 | 9:97,088,201 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.