FMNL2
formin like 2
Summary
This gene encodes a formin-related protein. Formin-related proteins have been implicated in morphogenesis, cytokinesis, and cell polarity. Alternatively spliced transcript variants encoding different isoforms have been described but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10497100 | 2:153,211,868 | T/G | — | — |
| rs7588008 | 2:153,212,316 | C/T | regulatory region variant | — |
| rs12614608 | 2:153,331,546 | G/C | — | — |
| rs6434068 | 2:153,357,541 | G/C | intron variant | — |
| rs1579050 | 2:153,364,527 | A/G | regulatory region variant | — |
| rs4664114 | 2:153,378,459 | T/C | — | benign |
| rs189416564 | 2:153,405,580 | C/G | — | likely benign |
| rs1695370663 | 2:153,415,301 | T/C | — | likely pathogenic |
| rs201635793 | 2:153,415,333 | G/T | — | uncertain significance |
| rs751675473 | 2:153,417,459 | G/T | — | uncertain significance |
| rs768389026 | 2:153,417,525 | G/A | — | uncertain significance |
| rs750994513 | 2:153,417,557 | C/G | — | likely benign |
| rs952649959 | 2:153,435,470 | G/T | — | uncertain significance |
| rs11675841 | 2:153,436,570 | C/T | intron variant | — |
| rs2468320568 | 2:153,437,475 | A/C | — | uncertain significance |
| rs1180261451 | 2:153,437,478 | C/G | — | uncertain significance |
| rs186698342 | 2:153,437,504 | G/A | — | uncertain significance |
| rs201721916 | 2:153,463,871 | C/T | — | uncertain significance |
| rs377497365 | 2:153,463,872 | G/A | — | uncertain significance |
| rs34119671 | 2:153,468,112 | A/G | — | benign |
| rs371415310 | 2:153,473,652 | T/G | — | uncertain significance |
| rs1367663865 | 2:153,475,519 | G/A | — | uncertain significance |
| rs1025133270 | 2:153,475,547 | C/T | — | uncertain significance |
| rs372473891 | 2:153,475,559 | G/A | — | uncertain significance |
| rs191661281 | 2:153,475,663 | C/T | — | likely benign |
| rs1209838801 | 2:153,476,028 | A/G | — | uncertain significance |
| rs578243842 | 2:153,476,095 | C/T | — | uncertain significance |
| rs1477757507 | 2:153,476,103 | C/T | — | uncertain significance |
| rs199752373 | 2:153,476,155 | T/C | — | uncertain significance |
| rs373279722 | 2:153,476,206 | C/T | — | uncertain significance |
| rs186945619 | 2:153,481,944 | G/A | — | likely benign |
| rs755228626 | 2:153,482,033 | A/G | — | uncertain significance |
| rs368512957 | 2:153,483,239 | T/C | — | likely benign |
| rs770656918 | 2:153,484,819 | C/A | — | uncertain significance |
| rs754245048 | 2:153,484,878 | A/G | — | uncertain significance |
| rs1164935476 | 2:153,484,898 | C/T | — | uncertain significance |
| rs1226633961 | 2:153,484,919 | C/T | — | uncertain significance |
| rs1028813684 | 2:153,492,946 | C/T | — | uncertain significance |
| rs1682612020 | 2:153,492,967 | G/A | — | uncertain significance |
| rs1412659657 | 2:153,493,021 | G/C | — | uncertain significance |
| rs2468677589 | 2:153,493,069 | C/A | — | uncertain significance |
| rs374183349 | 2:153,494,170 | G/T | — | likely benign |
| rs575556090 | 2:153,497,345 | T/C | — | uncertain significance |
| rs922398872 | 2:153,497,363 | G/A | — | uncertain significance |
| rs182064759 | 2:153,504,371 | T/G | — | uncertain significance |
| rs1683753128 | 2:153,504,396 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.