| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.55276221G>A | CA139610891 | HCRTR2 | c.763-1159G>A (n.763-1159G>A) c.568-1159G>A (n.568-1159G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.55276221G>C | CA567488243 | HCRTR2 | c.763-1159G>C (n.763-1159G>C) c.568-1159G>C (n.568-1159G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.55276221G= | CA2580593139 | HCRTR2 | c.763-1159G= (n.763-1159G=) c.568-1159G= (n.568-1159G=) | |
| 6 | g.55276221G>T | CA2580593138 | HCRTR2 | c.763-1159G>T (n.763-1159G>T) c.568-1159G>T (n.568-1159G>T) | |
| 6 | g.55276222A>G | CA826030883 | HCRTR2 | c.763-1158A>G (n.763-1158A>G) c.568-1158A>G (n.568-1158A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276224A>G | CA1089240322 | HCRTR2 | c.763-1156A>G (n.763-1156A>G) c.568-1156A>G (n.568-1156A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276231A>G | CA139610892 | HCRTR2 | c.763-1149A>G (n.763-1149A>G) c.568-1149A>G (n.568-1149A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276240C>A | CA1089240328 | HCRTR2 | c.763-1140C>A (n.763-1140C>A) c.568-1140C>A (n.568-1140C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276244T>C | CA1089240329 | HCRTR2 | c.763-1136T>C (n.763-1136T>C) c.568-1136T>C (n.568-1136T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276245C>T | CA2711803650 | HCRTR2 | c.763-1135C>T (n.763-1135C>T) c.568-1135C>T (n.568-1135C>T) | dbSNP |
| 6 | g.55276248T>C | CA1089240333 | HCRTR2 | c.763-1132T>C (n.763-1132T>C) c.568-1132T>C (n.568-1132T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276251T>A | CA139610893 | HCRTR2 | c.763-1129T>A (n.763-1129T>A) c.568-1129T>A (n.568-1129T>A) | dbSNP |
| 6 | g.55276253A>G | CA2711609666 | HCRTR2 | c.763-1127A>G (n.763-1127A>G) c.568-1127A>G (n.568-1127A>G) | dbSNP |
| 6 | g.55276257C>A | CA1089240340 | HCRTR2 | c.763-1123C>A (n.763-1123C>A) c.568-1123C>A (n.568-1123C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276264C>G | CA2711609667 | HCRTR2 | c.763-1116C>G (n.763-1116C>G) c.568-1116C>G (n.568-1116C>G) | dbSNP |
| 6 | g.55276265T>C | CA139610894 | HCRTR2 | c.763-1115T>C (n.763-1115T>C) c.568-1115T>C (n.568-1115T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.55276267T>C | CA2711609670 | HCRTR2 | c.763-1113T>C (n.763-1113T>C) c.568-1113T>C (n.568-1113T>C) | dbSNP |
| 6 | g.55276269C>T | CA139610895 | HCRTR2 | c.763-1111C>T (n.763-1111C>T) c.568-1111C>T (n.568-1111C>T) | dbSNP |
| 6 | g.55276270A>G | CA1089240343 | HCRTR2 | c.763-1110A>G (n.763-1110A>G) c.568-1110A>G (n.568-1110A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276271A>G | CA2556715774 | HCRTR2 | c.763-1109A>G (n.763-1109A>G) c.568-1109A>G (n.568-1109A>G) | dbSNP |
| 6 | g.55276274A>C | CA2711609673 | HCRTR2 | c.763-1106A>C (n.763-1106A>C) c.568-1106A>C (n.568-1106A>C) | dbSNP |
| 6 | g.55276276G>C | CA2711609674 | HCRTR2 | c.763-1104G>C (n.763-1104G>C) c.568-1104G>C (n.568-1104G>C) | dbSNP |
| 6 | g.55276279A>G | CA2711803653 | HCRTR2 | c.763-1101A>G (n.763-1101A>G) c.568-1101A>G (n.568-1101A>G) | dbSNP |
| 6 | g.55276281T>C | CA139610896 | HCRTR2 | c.763-1099T>C (n.763-1099T>C) c.568-1099T>C (n.568-1099T>C) | dbSNP |
| 6 | g.55276282G>T | CA2711609675 | HCRTR2 | c.763-1098G>T (n.763-1098G>T) c.568-1098G>T (n.568-1098G>T) | dbSNP |
| 6 | g.55276284T>C | CA139610897 | HCRTR2 | c.763-1096T>C (n.763-1096T>C) c.568-1096T>C (n.568-1096T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.55276294T>C | CA1089240347 | HCRTR2 | c.763-1086T>C (n.763-1086T>C) c.568-1086T>C (n.568-1086T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276295G>T | CA2711609676 | HCRTR2 | c.763-1085G>T (n.763-1085G>T) c.568-1085G>T (n.568-1085G>T) | dbSNP |
| 6 | g.55276296T>C | CA650346619 | HCRTR2 | c.763-1084T>C (n.763-1084T>C) c.568-1084T>C (n.568-1084T>C) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 6 | g.55276297_55276304del | CA2497154672 | HCRTR2 | c.763-1083_763-1076del (n.763-1083_763-1076del) c.568-1083_568-1076del (n.568-1083_568-1076del) | dbSNP |
| 6 | g.55276308A>G | CA1089240350 | HCRTR2 | c.763-1072A>G (n.763-1072A>G) c.568-1072A>G (n.568-1072A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276314G>T | CA139610898 | HCRTR2 | c.763-1066G>T (n.763-1066G>T) c.568-1066G>T (n.568-1066G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.55276315T>C | CA139610899 | HCRTR2 | c.763-1065T>C (n.763-1065T>C) c.568-1065T>C (n.568-1065T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.55276321T>G | CA826030889 | HCRTR2 | c.763-1059T>G (n.763-1059T>G) c.568-1059T>G (n.568-1059T>G) | dbSNP gnomAD v3 gnomAD v4 |