Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.55276078G>A | CA139610880 | HCRTR2 | c.763-1302G>A (n.763-1302G>A) c.568-1302G>A (n.568-1302G>A) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276078G>C | CA826030833 | HCRTR2 | c.763-1302G>C (n.763-1302G>C) c.568-1302G>C (n.568-1302G>C) | dbSNP |
6 | g.55276080T>C | CA826030838 | HCRTR2 | c.763-1300T>C (n.763-1300T>C) c.568-1300T>C (n.568-1300T>C) | dbSNP |
6 | g.55276080T>G | CA1089240252 | HCRTR2 | c.763-1300T>G (n.763-1300T>G) c.568-1300T>G (n.568-1300T>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276087A>T | CA2711609617 | HCRTR2 | c.763-1293A>T (n.763-1293A>T) c.568-1293A>T (n.568-1293A>T) | dbSNP |
6 | g.55276089T>C | CA826030843 | HCRTR2 | c.763-1291T>C (n.763-1291T>C) c.568-1291T>C (n.568-1291T>C) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276090G>T | CA826030845 | HCRTR2 | c.763-1290G>T (n.763-1290G>T) c.568-1290G>T (n.568-1290G>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276092G>C | CA139610881 | HCRTR2 | c.763-1288G>C (n.763-1288G>C) c.568-1288G>C (n.568-1288G>C) | dbSNP |
6 | g.55276097A>C | CA139610882 | HCRTR2 | c.763-1283A>C (n.763-1283A>C) c.568-1283A>C (n.568-1283A>C) | dbSNP gnomAD v4 |
6 | g.55276097A>G | CA826030850 | HCRTR2 | c.763-1283A>G (n.763-1283A>G) c.568-1283A>G (n.568-1283A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276100G>C | CA567488232 | HCRTR2 | c.763-1280G>C (n.763-1280G>C) c.568-1280G>C (n.568-1280G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276101A>G | CA1089240266 | HCRTR2 | c.763-1279A>G (n.763-1279A>G) c.568-1279A>G (n.568-1279A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276102A>G | CA826030855 | HCRTR2 | c.763-1278A>G (n.763-1278A>G) c.568-1278A>G (n.568-1278A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276103G>T | CA2560890551 | HCRTR2 | c.763-1277G>T (n.763-1277G>T) c.568-1277G>T (n.568-1277G>T) | |
6 | g.55276108A>G | CA2771135241 | HCRTR2 | c.763-1272A>G (n.763-1272A>G) c.568-1272A>G (n.568-1272A>G) | |
6 | g.55276110T>C | CA2711609618 | HCRTR2 | c.763-1270T>C (n.763-1270T>C) c.568-1270T>C (n.568-1270T>C) | dbSNP |
6 | g.55276112C>A | CA2711803647 | HCRTR2 | c.763-1268C>A (n.763-1268C>A) c.568-1268C>A (n.568-1268C>A) | dbSNP |
6 | g.55276113C>T | CA1089240270 | HCRTR2 | c.763-1267C>T (n.763-1267C>T) c.568-1267C>T (n.568-1267C>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276115A>C | CA139610883 | HCRTR2 | c.763-1265A>C (n.763-1265A>C) c.568-1265A>C (n.568-1265A>C) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276115A>G | CA826030860 | HCRTR2 | c.763-1265A>G (n.763-1265A>G) c.568-1265A>G (n.568-1265A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276118T>C | CA567488233 | HCRTR2 | c.763-1262T>C (n.763-1262T>C) c.568-1262T>C (n.568-1262T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276118T>G | CA826030861 | HCRTR2 | c.763-1262T>G (n.763-1262T>G) c.568-1262T>G (n.568-1262T>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276119C>A | CA139610884 | HCRTR2 | c.763-1261C>A (n.763-1261C>A) c.568-1261C>A (n.568-1261C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276123C>A | CA2711803648 | HCRTR2 | c.763-1257C>A (n.763-1257C>A) c.568-1257C>A (n.568-1257C>A) | dbSNP |
6 | g.55276124C>T | CA2711609620 | HCRTR2 | c.763-1256C>T (n.763-1256C>T) c.568-1256C>T (n.568-1256C>T) | dbSNP |
6 | g.55276126A>G | CA2771135242 | HCRTR2 | c.763-1254A>G (n.763-1254A>G) c.568-1254A>G (n.568-1254A>G) | |
6 | g.55276127C>G | CA1089240280 | HCRTR2 | c.763-1253C>G (n.763-1253C>G) c.568-1253C>G (n.568-1253C>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276127C>T | CA2711609622 | HCRTR2 | c.763-1253C>T (n.763-1253C>T) c.568-1253C>T (n.568-1253C>T) | dbSNP |
6 | g.55276129A>G | CA139610885 | HCRTR2 | c.763-1251A>G (n.763-1251A>G) c.568-1251A>G (n.568-1251A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276138A>G | CA139610886 | HCRTR2 | c.763-1242A>G (n.763-1242A>G) c.568-1242A>G (n.568-1242A>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276139A>G | CA2711609623 | HCRTR2 | c.763-1241A>G (n.763-1241A>G) c.568-1241A>G (n.568-1241A>G) | dbSNP |
6 | g.55276143T>A | CA2711530935 | HCRTR2 | c.763-1237T>A (n.763-1237T>A) c.568-1237T>A (n.568-1237T>A) | dbSNP |
6 | g.55276143T>C | CA567488236 | HCRTR2 | c.763-1237T>C (n.763-1237T>C) c.568-1237T>C (n.568-1237T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276147G>A | CA826030864 | HCRTR2 | c.763-1233G>A (n.763-1233G>A) c.568-1233G>A (n.568-1233G>A) | dbSNP |
6 | g.55276150_55276151del | CA2771135243 | HCRTR2 | c.763-1230_763-1229del (n.763-1230_763-1229del) c.568-1230_568-1229del (n.568-1230_568-1229del) | |
6 | g.55276152A>T | CA2771135244 | HCRTR2 | c.763-1228A>T (n.763-1228A>T) c.568-1228A>T (n.568-1228A>T) | |
6 | g.55276153C>T | CA826030868 | HCRTR2 | c.763-1227C>T (n.763-1227C>T) c.568-1227C>T (n.568-1227C>T) | dbSNP |
6 | g.55276157T>C | CA567488238 | HCRTR2 | c.763-1223T>C (n.763-1223T>C) c.568-1223T>C (n.568-1223T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55276158A>G | CA2711609624 | HCRTR2 | c.763-1222A>G (n.763-1222A>G) c.568-1222A>G (n.568-1222A>G) | dbSNP |
6 | g.55276159C>A | CA139610887 | HCRTR2 | c.763-1221C>A (n.763-1221C>A) c.568-1221C>A (n.568-1221C>A) | dbSNP |
6 | g.55276160T>C | CA2711609642 | HCRTR2 | c.763-1220T>C (n.763-1220T>C) c.568-1220T>C (n.568-1220T>C) | dbSNP |
6 | g.55276161A>G | CA2711609653 | HCRTR2 | c.763-1219A>G (n.763-1219A>G) c.568-1219A>G (n.568-1219A>G) | dbSNP |
6 | g.55276161A>T | CA1089240287 | HCRTR2 | c.763-1219A>T (n.763-1219A>T) c.568-1219A>T (n.568-1219A>T) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276163G>A | CA139610888 | HCRTR2 | c.763-1217G>A (n.763-1217G>A) c.568-1217G>A (n.568-1217G>A) | dbSNP |
6 | g.55276169_55276170del | CA1089240289 | HCRTR2 | c.763-1211_763-1210del (n.763-1211_763-1210del) c.568-1211_568-1210del (n.568-1211_568-1210del) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276171G>A | CA2711609654 | HCRTR2 | c.763-1209G>A (n.763-1209G>A) c.568-1209G>A (n.568-1209G>A) | dbSNP |
6 | g.55276172A>G | CA2771135245 | HCRTR2 | c.763-1208A>G (n.763-1208A>G) c.568-1208A>G (n.568-1208A>G) | |
6 | g.55276172A>T | CA2711803649 | HCRTR2 | c.763-1208A>T (n.763-1208A>T) c.568-1208A>T (n.568-1208A>T) | dbSNP |
6 | g.55276173T>G | CA1089240290 | HCRTR2 | c.763-1207T>G (n.763-1207T>G) c.568-1207T>G (n.568-1207T>G) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.55276174T>C | CA567488240 | HCRTR2 | c.763-1206T>C (n.763-1206T>C) c.568-1206T>C (n.568-1206T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |