CTTNBP2
cortactin binding protein 2
Summary
This gene encodes a protein with six ankyrin repeats and several proline-rich regions. A similar gene in rat interacts with a central regulator of the actin cytoskeleton. [provided by RefSeq, Jul 2008]
Known Variants115 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs577718648 | 7:117,351,602 | G/T | — | uncertain significance |
| rs370798516 | 7:117,351,712 | G/A | — | uncertain significance |
| rs113820495 | 7:117,351,728 | T/G | — | benign |
| rs762215104 | 7:117,351,737 | G/A | — | uncertain significance |
| rs752347575 | 7:117,351,769 | C/G | — | uncertain significance |
| rs150547726 | 7:117,351,826 | A/G | — | benign |
| rs750303532 | 7:117,358,130 | C/A | — | uncertain significance |
| rs146299860 | 7:117,358,131 | C/T | — | uncertain significance |
| rs1355444319 | 7:117,358,144 | C/T | — | uncertain significance |
| rs770393389 | 7:117,359,586 | G/C | — | uncertain significance |
| rs916985638 | 7:117,359,619 | G/C | — | uncertain significance |
| rs771179521 | 7:117,359,664 | G/A | — | uncertain significance |
| rs1462245041 | 7:117,361,167 | T/C | — | uncertain significance |
| rs2485370550 | 7:117,364,672 | T/A | — | uncertain significance |
| rs142054374 | 7:117,364,751 | T/C | — | uncertain significance |
| rs145882289 | 7:117,364,770 | T/C | — | likely benign |
| rs145435806 | 7:117,364,779 | G/T | — | uncertain significance |
| rs1196692588 | 7:117,365,130 | G/A | — | uncertain significance |
| rs143800569 | 7:117,365,146 | T/C | — | likely benign |
| rs753907443 | 7:117,365,226 | C/T | — | uncertain significance |
| rs759014527 | 7:117,365,247 | C/G | — | uncertain significance |
| rs752342954 | 7:117,365,259 | T/C | — | uncertain significance |
| rs751397467 | 7:117,365,280 | C/T | — | uncertain significance |
| rs781254525 | 7:117,365,286 | C/T | — | uncertain significance |
| rs200533770 | 7:117,365,316 | C/A | — | likely benign |
| rs372987038 | 7:117,368,191 | T/C | — | uncertain significance |
| rs200212967 | 7:117,368,215 | G/C | — | uncertain significance |
| rs771517669 | 7:117,368,230 | G/A | — | uncertain significance |
| rs371160545 | 7:117,368,273 | C/T | — | uncertain significance |
| rs138129215 | 7:117,368,308 | G/A | — | likely benign |
| rs1481363036 | 7:117,368,314 | C/T | — | uncertain significance |
| rs2485444049 | 7:117,374,999 | G/T | — | uncertain significance |
| rs750789291 | 7:117,375,020 | C/T | — | uncertain significance |
| rs149557894 | 7:117,375,032 | G/A | — | uncertain significance |
| rs372382974 | 7:117,375,047 | G/A | — | uncertain significance |
| rs1173378922 | 7:117,375,106 | A/T | — | uncertain significance |
| rs62617115 | 7:117,375,374 | C/A | — | benign |
| rs766038165 | 7:117,375,394 | G/A | — | uncertain significance |
| rs2485449268 | 7:117,375,430 | A/G | — | uncertain significance |
| rs35239561 | 7:117,375,432 | G/T | — | benign |
| rs144204623 | 7:117,377,309 | C/T | intron variant | — |
| rs757278 | 7:117,377,645 | G/T | intron variant | — |
| rs2485510851 | 7:117,385,944 | C/G | — | uncertain significance |
| rs748714410 | 7:117,385,950 | A/G | — | uncertain significance |
| rs10274022 | 7:117,385,978 | G/T | — | benign |
| rs2485512456 | 7:117,386,135 | C/T | — | uncertain significance |
| rs1370037710 | 7:117,396,659 | T/C | — | uncertain significance |
| rs200975491 | 7:117,396,664 | C/A | — | likely benign |
| rs200124757 | 7:117,398,016 | G/A | — | uncertain significance |
| rs144920028 | 7:117,400,548 | T/C | — | uncertain significance |
| rs2485596059 | 7:117,400,708 | C/G | — | uncertain significance |
| rs1797528056 | 7:117,407,181 | C/T | — | uncertain significance |
| rs770292782 | 7:117,407,206 | G/A | — | uncertain significance |
| rs75322384 | 7:117,417,559 | A/G | — | benign |
| rs998757505 | 7:117,417,575 | T/C | — | uncertain significance |
| rs559857978 | 7:117,417,583 | A/G | — | likely benign |
| rs774178944 | 7:117,417,593 | G/A | — | uncertain significance |
| rs1003026055 | 7:117,417,611 | C/T | — | uncertain significance |
| rs1178090016 | 7:117,417,674 | T/C | — | uncertain significance |
| rs1798184298 | 7:117,417,763 | C/G | — | uncertain significance |
| rs2485750853 | 7:117,420,571 | A/T | — | uncertain significance |
| rs2485784657 | 7:117,424,395 | T/A | — | uncertain significance |
| rs775511909 | 7:117,424,467 | G/C | — | uncertain significance |
| rs2116856261 | 7:117,431,224 | A/G | — | uncertain significance |
| rs116692992 | 7:117,431,308 | G/C | — | likely benign |
| rs1224391264 | 7:117,431,332 | G/A | — | uncertain significance |
| rs978782396 | 7:117,431,352 | G/A | — | uncertain significance |
| rs2485841772 | 7:117,431,356 | C/G | — | uncertain significance |
| rs2485843027 | 7:117,431,439 | G/C | — | uncertain significance |
| rs140806793 | 7:117,431,471 | T/C | — | likely benign |
| rs2485845463 | 7:117,431,617 | T/C | — | uncertain significance |
| rs2485845551 | 7:117,431,625 | G/A | — | uncertain significance |
| rs1281036488 | 7:117,431,650 | C/T | — | uncertain significance |
| rs1225367580 | 7:117,431,709 | G/C | — | uncertain significance |
| rs748410342 | 7:117,431,730 | G/A | — | uncertain significance |
| rs370391886 | 7:117,431,821 | T/C | — | uncertain significance |
| rs758282368 | 7:117,431,841 | G/A | — | uncertain significance |
| rs755053005 | 7:117,431,868 | T/C | — | uncertain significance |
| rs1266724644 | 7:117,431,943 | G/A | — | uncertain significance |
| rs1448826105 | 7:117,431,976 | A/G | — | uncertain significance |
| rs201811547 | 7:117,432,077 | T/G | — | likely benign |
| rs1200170708 | 7:117,432,142 | C/A | — | likely benign |
| rs1329181110 | 7:117,432,274 | T/C | — | likely benign |
| rs1799073506 | 7:117,432,318 | A/G | — | uncertain significance |
| rs541089121 | 7:117,432,384 | C/T | — | likely benign |
| rs751121520 | 7:117,432,402 | C/T | — | uncertain significance |
| rs1325968710 | 7:117,432,501 | G/A | — | uncertain significance |
| rs777931972 | 7:117,432,520 | T/C | — | uncertain significance |
| rs2485859536 | 7:117,432,544 | T/A | — | uncertain significance |
| rs772806857 | 7:117,432,583 | T/A | — | uncertain significance |
| rs1319157563 | 7:117,432,586 | C/T | — | uncertain significance |
| rs746326027 | 7:117,432,597 | C/T | — | likely benign |
| rs1301550777 | 7:117,432,636 | T/G | — | uncertain significance |
| rs2485860954 | 7:117,432,652 | C/T | — | uncertain significance |
| rs769208688 | 7:117,432,667 | C/T | — | likely benign |
| rs375304355 | 7:117,432,774 | C/T | — | uncertain significance |
| rs34868515 | 7:117,450,810 | C/T | — | benign |
| rs143605688 | 7:117,450,854 | C/T | — | likely benign |
| rs368768466 | 7:117,451,011 | C/T | — | likely benign |
| rs753298694 | 7:117,451,013 | G/A | — | uncertain significance |
Showing 100 of 115 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.