SYNE2
spectrin repeat containing nuclear envelope protein 2
Summary
The protein encoded by this gene is a nuclear outer membrane protein that binds cytoplasmic F-actin. This binding tethers the nucleus to the cytoskeleton and aids in the maintenance of the structural integrity of the nucleus. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
Known Variants3,504 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12879147 | 14:64,227,596 | G/A | upstream gene variant | — |
| rs7160525 | 14:64,232,220 | G/C | — | — |
| rs17101394 | 14:64,232,386 | G/C | — | — |
| rs8008068 | 14:64,233,717 | A/G | downstream gene variant | — |
| rs8008070 | 14:64,233,720 | A/C | — | — |
| rs8012828 | 14:64,233,980 | C/T | intergenic variant | — |
| rs4902243 | 14:64,234,243 | A/T | — | — |
| rs7157785 | 14:64,235,556 | G/T | intergenic variant | — |
| rs35372182 | 14:64,236,157 | A/G | intergenic variant | — |
| rs12880341 | 14:64,236,191 | T/C | intergenic variant | — |
| rs183105427 | 14:64,236,343 | C/T | intergenic variant | — |
| rs12897637 | 14:64,239,351 | T/C | intergenic variant | — |
| rs12878001 | 14:64,239,629 | T/G | intergenic variant | — |
| rs113188193 | 14:64,240,903 | T/G | — | — |
| rs142969393 | 14:64,241,684 | A/G | intergenic variant | — |
| rs116982134 | 14:64,242,855 | T/C | intergenic variant | — |
| rs11848860 | 14:64,245,938 | G/A | intergenic variant | — |
| rs2356994 | 14:64,246,329 | T/A | intergenic variant | — |
| rs35635100 | 14:64,248,929 | C/G | — | — |
| rs4591051 | 14:64,251,357 | A/C | intergenic variant | — |
| rs114540020 | 14:64,255,411 | A/C | — | — |
| rs186113455 | 14:64,268,359 | T/C | intergenic variant | — |
| rs139820814 | 14:64,272,957 | G/A | upstream gene variant | — |
| rs7144584 | 14:64,275,812 | T/A | — | — |
| rs7148584 | 14:64,276,192 | G/A | — | — |
| rs142689528 | 14:64,281,816 | A/G | intergenic variant | — |
| rs36144365 | 14:64,281,937 | T/G | — | — |
| rs77115255 | 14:64,287,430 | A/G | intergenic variant | — |
| rs8007407 | 14:64,289,629 | G/A | intergenic variant | — |
| rs141002745 | 14:64,289,988 | C/T | intergenic variant | — |
| rs146819908 | 14:64,297,720 | G/A | intergenic variant | — |
| rs117393850 | 14:64,299,069 | G/A | intergenic variant | — |
| rs117152834 | 14:64,300,828 | C/T | intergenic variant | — |
| rs149449980 | 14:64,301,005 | C/T | intergenic variant | — |
| rs148202809 | 14:64,301,111 | C/T | intergenic variant | — |
| rs144465871 | 14:64,302,825 | G/A | intergenic variant | — |
| rs117030110 | 14:64,303,835 | A/G | intergenic variant | — |
| rs75958579 | 14:64,306,334 | G/T | — | — |
| rs145218204 | 14:64,307,928 | C/T | regulatory region variant | — |
| rs2104795 | 14:64,308,832 | G/A | intergenic variant | — |
| rs139278298 | 14:64,311,814 | T/C | — | — |
| rs138410811 | 14:64,316,180 | T/C | upstream gene variant | — |
| rs143315154 | 14:64,319,689 | C/T | — | benign |
| rs886050574 | 14:64,319,704 | A/T | — | uncertain significance |
| rs552973060 | 14:64,319,711 | G/C | — | benign |
| rs886050575 | 14:64,319,744 | C/T | — | uncertain significance |
| rs926052381 | 14:64,319,764 | G/A | — | uncertain significance |
| rs886050576 | 14:64,319,785 | A/T | — | uncertain significance |
| rs886050577 | 14:64,319,806 | G/A | — | uncertain significance |
| rs1393089319 | 14:64,319,861 | G/A | — | uncertain significance |
| rs535493323 | 14:64,319,870 | G/A | — | benign |
| rs118024635 | 14:64,326,975 | C/A | intron variant | — |
| rs954730 | 14:64,330,196 | A/C | regulatory region variant | — |
| rs144245540 | 14:64,332,488 | A/C | — | — |
| rs12878037 | 14:64,336,630 | C/T | — | — |
| rs149809141 | 14:64,339,365 | G/A | intron variant | — |
| rs79864379 | 14:64,339,767 | G/C | intron variant | — |
| rs8015354 | 14:64,340,321 | A/C | — | — |
| rs66684280 | 14:64,349,595 | G/T | intron variant | — |
| rs8023195 | 14:64,350,775 | G/C | intron variant | — |
| rs368225478 | 14:64,375,872 | A/G | — | likely benign |
| rs750823503 | 14:64,375,877 | G/A | — | uncertain significance |
| rs2153351102 | 14:64,375,881 | T/C | — | likely benign |
| rs2095442604 | 14:64,375,884 | G/C | — | uncertain significance |
| rs2275017 | 14:64,375,888 | C/T | — | likely benign |
| rs755131989 | 14:64,375,893 | C/T | — | likely benign |
| rs781375790 | 14:64,375,894 | G/C | — | uncertain significance |
| rs901997575 | 14:64,375,898 | A/C | — | uncertain significance |
| rs1187262903 | 14:64,375,905 | G/T | — | uncertain significance |
| rs372179532 | 14:64,375,920 | C/T | — | likely benign |
| rs1011315005 | 14:64,375,921 | G/A | — | uncertain significance |
| rs749130552 | 14:64,375,923 | C/T | — | likely benign |
| rs770930910 | 14:64,375,924 | G/T | — | uncertain significance |
| rs2550192630 | 14:64,375,932 | T/C | — | likely benign |
| rs760448281 | 14:64,375,948 | A/T | — | uncertain significance |
| rs776230510 | 14:64,375,950 | T/A | — | uncertain significance |
| rs752893186 | 14:64,375,964 | G/A | — | benign |
| rs2275018 | 14:64,375,985 | T/G | — | benign |
| rs8007892 | 14:64,386,454 | A/C | — | — |
| rs12878312 | 14:64,394,600 | A/T | — | benign |
| rs4902258 | 14:64,406,690 | A/C | intron variant | — |
| rs3742619 | 14:64,407,175 | C/G | — | benign |
| rs2550509918 | 14:64,407,318 | T/A | — | likely benign |
| rs1347408215 | 14:64,407,321 | T/G | — | likely benign |
| rs769250456 | 14:64,407,325 | T/G | — | likely benign |
| rs774804800 | 14:64,407,328 | A/G | — | likely benign |
| rs754068232 | 14:64,407,365 | C/T | — | uncertain significance |
| rs369020126 | 14:64,407,366 | G/A | — | uncertain significance |
| rs779957646 | 14:64,407,376 | A/G | — | uncertain significance |
| rs746827264 | 14:64,407,378 | C/G | — | uncertain significance |
| rs754783984 | 14:64,407,380 | C/T | — | uncertain significance |
| rs780891110 | 14:64,407,381 | A/T | — | likely benign |
| rs772731543 | 14:64,407,392 | G/A | — | uncertain significance |
| rs1453226677 | 14:64,407,405 | A/C | — | likely benign |
| rs772572092 | 14:64,407,411 | A/G | — | likely benign |
| rs2275019 | 14:64,408,108 | G/C | intron variant | — |
| rs2184292 | 14:64,408,135 | A/C | — | benign |
| rs794727659 | 14:64,408,413 | C/T | — | uncertain significance |
| rs751515594 | 14:64,408,415 | C/T | — | likely benign |
| rs754768287 | 14:64,408,417 | C/G | — | uncertain significance |
Showing 100 of 3,504 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.