M1AP
meiosis 1 associated protein
Summary
This gene encodes a protein that is likely to function in progression of meiosis. A similar protein in mouse plays a role in gametogenesis in both sexes. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1677697539 | 2:74,786,002 | C/T | — | pathogenic |
| rs200875527 | 2:74,787,285 | G/A | — | likely benign |
| rs200216388 | 2:74,787,286 | G/A | — | uncertain significance |
| rs753332334 | 2:74,787,291 | C/T | — | uncertain significance |
| rs367678611 | 2:74,787,394 | C/G | — | uncertain significance |
| rs762163965 | 2:74,787,411 | A/G | — | uncertain significance |
| rs143680043 | 2:74,789,349 | C/T | — | uncertain significance |
| rs745610891 | 2:74,789,392 | G/A | — | likely benign |
| rs773436081 | 2:74,789,420 | G/A | — | uncertain significance |
| rs751126701 | 2:74,789,459 | G/A | — | uncertain significance |
| rs11126435 | 2:74,789,700 | A/C | — | — |
| rs979521322 | 2:74,798,514 | G/A | — | — |
| rs1679010214 | 2:74,802,668 | T/C | — | uncertain significance |
| rs140179344 | 2:74,802,690 | C/T | — | uncertain significance |
| rs755225252 | 2:74,803,654 | T/C | — | uncertain significance |
| rs200989583 | 2:74,803,673 | A/C | — | uncertain significance |
| rs142319651 | 2:74,803,676 | G/A | — | uncertain significance |
| rs149272394 | 2:74,803,718 | C/T | — | uncertain significance |
| rs1169183061 | 2:74,803,742 | C/T | — | uncertain significance |
| rs201780018 | 2:74,803,744 | C/T | — | uncertain significance |
| rs754324894 | 2:74,808,921 | C/T | — | uncertain significance |
| rs2530285945 | 2:74,808,968 | G/C | — | uncertain significance |
| rs2530458075 | 2:74,834,179 | T/C | — | uncertain significance |
| rs1364843927 | 2:74,834,220 | A/T | — | uncertain significance |
| rs1008736046 | 2:74,834,275 | C/T | — | uncertain significance |
| rs1233937726 | 2:74,834,340 | A/G | — | uncertain significance |
| rs559352253 | 2:74,842,123 | T/C | — | uncertain significance |
| rs34629223 | 2:74,842,151 | T/C | — | likely benign |
| rs563816801 | 2:74,842,173 | G/A | — | likely pathogenic, low penetrance |
| rs769111357 | 2:74,842,180 | G/A | — | uncertain significance |
| rs2530527112 | 2:74,842,192 | C/T | — | uncertain significance |
| rs977110652 | 2:74,842,224 | A/G | — | uncertain significance |
| rs2530527991 | 2:74,842,242 | C/G | — | uncertain significance |
| rs759509912 | 2:74,842,243 | A/C | — | uncertain significance |
| rs767684661 | 2:74,842,263 | T/C | — | uncertain significance |
| rs369692295 | 2:74,867,206 | A/G | — | uncertain significance |
| rs374080806 | 2:74,867,224 | C/T | — | uncertain significance |
| rs1573195678 | 2:74,867,255 | A/G | — | uncertain significance |
| rs2530700563 | 2:74,867,278 | C/T | — | uncertain significance |
| rs368985707 | 2:74,867,359 | G/A | — | uncertain significance |
| rs1203549551 | 2:74,867,366 | T/C | — | uncertain significance |
| rs149981067 | 2:74,867,398 | T/A | — | uncertain significance |
| rs568602257 | 2:74,867,534 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.