FER1L5
fer-1 like family member 5
Summary
Predicted to enable calcium ion binding activity. Predicted to be involved in regulation of neurotransmitter secretion. Predicted to be located in plasma membrane. Predicted to be active in synaptic vesicle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants124 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371465306 | 2:97,308,632 | G/C | — | uncertain significance |
| rs368841036 | 2:97,312,179 | G/A | — | uncertain significance |
| rs779752178 | 2:97,312,825 | C/T | — | uncertain significance |
| rs749243667 | 2:97,312,838 | A/C | — | uncertain significance |
| rs200413243 | 2:97,313,565 | G/A | — | uncertain significance |
| rs775852542 | 2:97,315,366 | G/A | — | uncertain significance |
| rs1437422684 | 2:97,315,399 | G/T | — | uncertain significance |
| rs377426781 | 2:97,315,989 | C/T | — | likely benign |
| rs928481263 | 2:97,317,723 | G/A | — | uncertain significance |
| rs571426604 | 2:97,317,754 | T/G | — | uncertain significance |
| rs2468836777 | 2:97,319,384 | T/C | — | uncertain significance |
| rs749485474 | 2:97,327,462 | G/C | — | uncertain significance |
| rs867002330 | 2:97,327,510 | G/A | — | uncertain significance |
| rs367710609 | 2:97,329,195 | C/A | — | uncertain significance |
| rs758909332 | 2:97,329,203 | G/A | — | uncertain significance |
| rs142154282 | 2:97,329,237 | G/A | — | likely benign |
| rs187155661 | 2:97,334,625 | G/A | — | likely benign |
| rs552466206 | 2:97,334,640 | C/T | — | uncertain significance |
| rs1267013337 | 2:97,334,682 | C/T | — | uncertain significance |
| rs1327758658 | 2:97,334,720 | G/C | — | uncertain significance |
| rs2468961537 | 2:97,334,732 | T/C | — | likely benign |
| rs373702127 | 2:97,334,782 | G/C | — | uncertain significance |
| rs952373573 | 2:97,334,818 | T/G | — | uncertain significance |
| rs372587766 | 2:97,335,910 | G/C | — | uncertain significance |
| rs114142480 | 2:97,350,113 | C/T | — | benign |
| rs200295527 | 2:97,350,120 | T/G | — | uncertain significance |
| rs570761089 | 2:97,350,184 | G/A | — | uncertain significance |
| rs772097939 | 2:97,351,075 | C/A | — | uncertain significance |
| rs1296757348 | 2:97,351,079 | A/G | — | uncertain significance |
| rs1261041481 | 2:97,351,687 | C/T | — | uncertain significance |
| rs2469086124 | 2:97,351,706 | C/T | — | uncertain significance |
| rs778452251 | 2:97,351,711 | G/A | — | uncertain significance |
| rs868457088 | 2:97,351,814 | C/T | — | likely benign |
| rs372356350 | 2:97,351,831 | C/T | — | uncertain significance |
| rs7599598 | 2:97,351,840 | A/G | — | benign |
| rs545151195 | 2:97,352,014 | C/G | — | uncertain significance |
| rs776051668 | 2:97,352,016 | G/A | — | likely benign |
| rs1199434553 | 2:97,352,037 | G/C | — | likely benign |
| rs769303983 | 2:97,352,049 | G/C | — | uncertain significance |
| rs1261398607 | 2:97,353,607 | A/G | — | uncertain significance |
| rs777387964 | 2:97,353,653 | G/A | — | uncertain significance |
| rs912266983 | 2:97,353,676 | G/A | — | uncertain significance |
| rs767948815 | 2:97,355,050 | C/T | — | uncertain significance |
| rs1240825951 | 2:97,355,062 | C/T | — | uncertain significance |
| rs948092700 | 2:97,355,388 | C/G | — | uncertain significance |
| rs1490003435 | 2:97,355,445 | C/T | — | uncertain significance |
| rs2077129811 | 2:97,356,977 | A/G | — | uncertain significance |
| rs980439955 | 2:97,357,002 | C/T | — | uncertain significance |
| rs757825382 | 2:97,357,013 | C/T | — | uncertain significance |
| rs1014851606 | 2:97,357,023 | C/T | — | likely benign |
| rs914070209 | 2:97,357,026 | G/T | — | uncertain significance |
| rs781178713 | 2:97,357,032 | G/T | — | uncertain significance |
| rs1182476506 | 2:97,357,067 | G/A | — | uncertain significance |
| rs2469143402 | 2:97,357,071 | C/T | — | uncertain significance |
| rs748882176 | 2:97,357,238 | C/G | — | uncertain significance |
| rs954217634 | 2:97,357,263 | C/T | — | uncertain significance |
| rs563011812 | 2:97,357,264 | G/A | — | uncertain significance |
| rs1050042425 | 2:97,357,269 | C/T | — | uncertain significance |
| rs985389957 | 2:97,357,270 | G/A | — | uncertain significance |
| rs1268232963 | 2:97,357,284 | C/T | — | uncertain significance |
| rs1453552518 | 2:97,357,285 | G/A | — | likely benign |
| rs371667746 | 2:97,357,288 | G/A | — | uncertain significance |
| rs1200552242 | 2:97,357,464 | G/T | — | uncertain significance |
| rs71427090 | 2:97,357,466 | G/A | — | uncertain significance |
| rs190249640 | 2:97,357,566 | T/C | — | uncertain significance |
| rs564412642 | 2:97,357,613 | C/G | — | uncertain significance |
| rs769337167 | 2:97,357,676 | C/A | — | uncertain significance |
| rs918611246 | 2:97,357,679 | T/C | — | uncertain significance |
| rs777639564 | 2:97,357,883 | G/A | — | uncertain significance |
| rs555171579 | 2:97,359,300 | G/A | — | uncertain significance |
| rs1329029114 | 2:97,359,317 | T/A | — | uncertain significance |
| rs747881322 | 2:97,359,669 | C/T | — | uncertain significance |
| rs540774404 | 2:97,359,687 | A/G | — | likely benign |
| rs1400736380 | 2:97,359,697 | T/A | — | uncertain significance |
| rs905576885 | 2:97,359,724 | C/G | — | uncertain significance |
| rs2077260727 | 2:97,359,727 | T/C | — | uncertain significance |
| rs2469174625 | 2:97,359,728 | G/A | — | uncertain significance |
| rs764285594 | 2:97,359,768 | G/A | — | uncertain significance |
| rs898404728 | 2:97,360,164 | A/G | — | uncertain significance |
| rs769615665 | 2:97,361,489 | C/T | — | uncertain significance |
| rs1158895223 | 2:97,361,495 | A/C | — | uncertain significance |
| rs1211370263 | 2:97,361,545 | G/A | — | uncertain significance |
| rs200034058 | 2:97,361,561 | C/T | — | uncertain significance |
| rs567730226 | 2:97,361,579 | A/T | — | uncertain significance |
| rs1237809476 | 2:97,361,611 | G/A | — | uncertain significance |
| rs765966910 | 2:97,361,629 | C/A | — | uncertain significance |
| rs371201997 | 2:97,361,789 | C/T | — | uncertain significance |
| rs2469198495 | 2:97,361,802 | G/T | — | uncertain significance |
| rs1458896102 | 2:97,363,290 | T/C | — | uncertain significance |
| rs1221100218 | 2:97,363,312 | A/T | — | uncertain significance |
| rs777953710 | 2:97,363,434 | T/C | — | uncertain significance |
| rs749358861 | 2:97,363,798 | G/A | — | uncertain significance |
| rs374460728 | 2:97,363,804 | G/A | — | uncertain significance |
| rs184478113 | 2:97,363,843 | C/A | — | uncertain significance |
| rs760559628 | 2:97,363,849 | C/G | — | uncertain significance |
| rs764708234 | 2:97,363,876 | G/A | — | uncertain significance |
| rs202240902 | 2:97,364,795 | T/C | — | uncertain significance |
| rs745681758 | 2:97,364,831 | G/A | — | uncertain significance |
| rs2469235087 | 2:97,365,421 | T/C | — | uncertain significance |
| rs766627541 | 2:97,365,689 | G/A | — | uncertain significance |
Showing 100 of 124 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.