Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.52322338_52322372del | CA963156572 | PTGER2 | c.844-4883_844-4849del (n.844-4883_844-4849del) c.79-4883_79-4849del (n.79-4883_79-4849del) | gnomAD v3 gnomAD v4 |
14 | g.52322367_52322368insTCCTCAGAACAT | CA919419249 | PTGER2 | c.844-4854_844-4853insTCCTCAGAACAT (n.844-4854_844-4853insTCCTCAGAACAT) c.79-4854_79-4853insTCCTCAGAACAT (n.79-4854_79-4853insTCCTCAGAACAT) | dbSNP |
14 | g.52322366A= | CA2137042205 | PTGER2 | c.844-4855A= (n.844-4855A=) c.79-4855A= (n.79-4855A=) | |
14 | g.52322366A>G | CA963156582 | PTGER2 | c.844-4855A>G (n.844-4855A>G) c.79-4855A>G (n.79-4855A>G) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322369C= | CA2137042207 | PTGER2 | c.844-4852C= (n.844-4852C=) c.79-4852C= (n.79-4852C=) | |
14 | g.52322369C>G | CA260917495 | PTGER2 | c.844-4852C>G (n.844-4852C>G) c.79-4852C>G (n.79-4852C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322371T>C | CA2137042208 | PTGER2 | c.844-4850T>C (n.844-4850T>C) c.79-4850T>C (n.79-4850T>C) | dbSNP |
14 | g.52322371T= | CA2137042209 | PTGER2 | c.844-4850T= (n.844-4850T=) c.79-4850T= (n.79-4850T=) | |
14 | g.52322374G= | CA2137042211 | PTGER2 | c.844-4847G= (n.844-4847G=) c.79-4847G= (n.79-4847G=) | |
14 | g.52322374G>T | CA706696604 | PTGER2 | c.844-4847G>T (n.844-4847G>T) c.79-4847G>T (n.79-4847G>T) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322380A= | CA2137042215 | PTGER2 | c.844-4841A= (n.844-4841A=) c.79-4841A= (n.79-4841A=) | |
14 | g.52322380A>T | CA260917500 | PTGER2 | c.844-4841A>T (n.844-4841A>T) c.79-4841A>T (n.79-4841A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322381C= | CA2137042218 | PTGER2 | c.844-4840C= (n.844-4840C=) c.79-4840C= (n.79-4840C=) | |
14 | g.52322381C>G | CA2137042220 | PTGER2 | c.844-4840C>G (n.844-4840C>G) c.79-4840C>G (n.79-4840C>G) | dbSNP |
14 | g.52322386C= | CA2137042223 | PTGER2 | c.844-4835C= (n.844-4835C=) c.79-4835C= (n.79-4835C=) | |
14 | g.52322386C>G | CA963156585 | PTGER2 | c.844-4835C>G (n.844-4835C>G) c.79-4835C>G (n.79-4835C>G) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322389G>A | CA2137042227 | PTGER2 | c.844-4832G>A (n.844-4832G>A) c.79-4832G>A (n.79-4832G>A) | dbSNP |
14 | g.52322389G= | CA2137042226 | PTGER2 | c.844-4832G= (n.844-4832G=) c.79-4832G= (n.79-4832G=) | |
14 | g.52322390G>A | CA963156586 | PTGER2 | c.844-4831G>A (n.844-4831G>A) c.79-4831G>A (n.79-4831G>A) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322390G= | CA2137042230 | PTGER2 | c.844-4831G= (n.844-4831G=) c.79-4831G= (n.79-4831G=) | |
14 | g.52322391G>A | CA2137042233 | PTGER2 | c.844-4830G>A (n.844-4830G>A) c.79-4830G>A (n.79-4830G>A) | dbSNP |
14 | g.52322391G= | CA2137042232 | PTGER2 | c.844-4830G= (n.844-4830G=) c.79-4830G= (n.79-4830G=) | |
14 | g.52322391G>T | CA2801588201 | PTGER2 | c.844-4830G>T (n.844-4830G>T) c.79-4830G>T (n.79-4830G>T) | |
14 | g.52322392C= | CA2137042236 | PTGER2 | c.844-4829C= (n.844-4829C=) c.79-4829C= (n.79-4829C=) | |
14 | g.52322392C>T | CA613904718 | PTGER2 | c.844-4829C>T (n.844-4829C>T) c.79-4829C>T (n.79-4829C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322400G>A | CA2137042243 | PTGER2 | c.844-4821G>A (n.844-4821G>A) c.79-4821G>A (n.79-4821G>A) | dbSNP |
14 | g.52322400G= | CA2137042240 | PTGER2 | c.844-4821G= (n.844-4821G=) c.79-4821G= (n.79-4821G=) | |
14 | g.52322403A= | CA2137042245 | PTGER2 | c.844-4818A= (n.844-4818A=) c.79-4818A= (n.79-4818A=) | |
14 | g.52322403A>G | CA260917506 | PTGER2 | c.844-4818A>G (n.844-4818A>G) c.79-4818A>G (n.79-4818A>G) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322405T>A | CA2137042252 | PTGER2 | c.844-4816T>A (n.844-4816T>A) c.79-4816T>A (n.79-4816T>A) | dbSNP |
14 | g.52322405T= | CA2137042250 | PTGER2 | c.844-4816T= (n.844-4816T=) c.79-4816T= (n.79-4816T=) | |
14 | g.52322406C>A | CA963156588 | PTGER2 | c.844-4815C>A (n.844-4815C>A) c.79-4815C>A (n.79-4815C>A) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322406C= | CA2137042256 | PTGER2 | c.844-4815C= (n.844-4815C=) c.79-4815C= (n.79-4815C=) | |
14 | g.52322412A= | CA2137042257 | PTGER2 | c.844-4809A= (n.844-4809A=) c.79-4809A= (n.79-4809A=) | |
14 | g.52322412A>C | CA613904720 | PTGER2 | c.844-4809A>C (n.844-4809A>C) c.79-4809A>C (n.79-4809A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322413A= | CA2137042259 | PTGER2 | c.844-4808A= (n.844-4808A=) c.79-4808A= (n.79-4808A=) | |
14 | g.52322413A>G | CA963156590 | PTGER2 | c.844-4808A>G (n.844-4808A>G) c.79-4808A>G (n.79-4808A>G) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322414G>A | CA2137042261 | PTGER2 | c.844-4807G>A (n.844-4807G>A) c.79-4807G>A (n.79-4807G>A) | dbSNP |
14 | g.52322414G= | CA2137042260 | PTGER2 | c.844-4807G= (n.844-4807G=) c.79-4807G= (n.79-4807G=) | |
14 | g.52322421A= | CA2137042264 | PTGER2 | c.844-4800A= (n.844-4800A=) c.79-4800A= (n.79-4800A=) | |
14 | g.52322421A>G | CA2137042265 | PTGER2 | c.844-4800A>G (n.844-4800A>G) c.79-4800A>G (n.79-4800A>G) | dbSNP |
14 | g.52322421_52322448delinsACAAAGATCACAAGGCAAAGGGCAAAAG | CA2137042263 | PTGER2 | c.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG (n.844-4800_844-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG) c.79-4800_79-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG (n.79-4800_79-4773delinsACAAAGATCACAAGGCAAAGGGCAAAAG) | |
14 | g.52322422_52322424delinsCAA | CA2137042269 | PTGER2 | c.844-4799_844-4797delinsCAA (n.844-4799_844-4797delinsCAA) c.79-4799_79-4797delinsCAA (n.79-4799_79-4797delinsCAA) | |
14 | g.52322451_52322477del | CA613904721 | PTGER2 | c.844-4770_844-4744del (n.844-4770_844-4744del) c.79-4770_79-4744del (n.79-4770_79-4744del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322424_52322425del | CA613904722 | PTGER2 | c.844-4797_844-4796del (n.844-4797_844-4796del) c.79-4797_79-4796del (n.79-4797_79-4796del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322424A= | CA2137042275 | PTGER2 | c.844-4797A= (n.844-4797A=) c.79-4797A= (n.79-4797A=) | |
14 | g.52322424A>G | CA15823555 | PTGER2 | c.844-4797A>G (n.844-4797A>G) c.79-4797A>G (n.79-4797A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322424A>T | CA2137042278 | PTGER2 | c.844-4797A>T (n.844-4797A>T) c.79-4797A>T (n.79-4797A>T) | dbSNP |
14 | g.52322426_52322451delinsGATCACAAGGCAAAGGGCAAAAGCAA | CA2137042280 | PTGER2 | c.844-4795_844-4770delinsGATCACAAGGCAAAGGGCAAAAGCAA (n.844-4795_844-4770delinsGATCACAAGGCAAAGGGCAAAAGCAA) c.79-4795_79-4770delinsGATCACAAGGCAAAGGGCAAAAGCAA (n.79-4795_79-4770delinsGATCACAAGGCAAAGGGCAAAAGCAA) | |
14 | g.52322428_52322452del | CA613904725 | PTGER2 | c.844-4793_844-4769del (n.844-4793_844-4769del) c.79-4793_79-4769del (n.79-4793_79-4769del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.52322435G>A | CA706696622 | PTGER2 | c.844-4786G>A (n.844-4786G>A) c.79-4786G>A (n.79-4786G>A) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322435G= | CA2137042288 | PTGER2 | c.844-4786G= (n.844-4786G=) c.79-4786G= (n.79-4786G=) | |
14 | g.52322442G>A | CA2137042296 | PTGER2 | c.844-4779G>A (n.844-4779G>A) c.79-4779G>A (n.79-4779G>A) | dbSNP |
14 | g.52322442G= | CA2137042295 | PTGER2 | c.844-4779G= (n.844-4779G=) c.79-4779G= (n.79-4779G=) | |
14 | g.52322443C>A | CA2137042306 | PTGER2 | c.844-4778C>A (n.844-4778C>A) c.79-4778C>A (n.79-4778C>A) | dbSNP |
14 | g.52322443C= | CA2137042305 | PTGER2 | c.844-4778C= (n.844-4778C=) c.79-4778C= (n.79-4778C=) | |
14 | g.52322443_52322444delinsCA | CA2137042300 | PTGER2 | c.844-4778_844-4777delinsCA (n.844-4778_844-4777delinsCA) c.79-4778_79-4777delinsCA (n.79-4778_79-4777delinsCA) | |
14 | g.52322447del | CA706696623 | PTGER2 | c.844-4774del (n.844-4774del) c.79-4774del (n.79-4774del) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322449C>A | CA2510206673 | PTGER2 | c.844-4772C>A (n.844-4772C>A) c.79-4772C>A (n.79-4772C>A) | |
14 | g.52322451A= | CA2137042309 | PTGER2 | c.844-4770A= (n.844-4770A=) c.79-4770A= (n.79-4770A=) | |
14 | g.52322451A>G | CA706696625 | PTGER2 | c.844-4770A>G (n.844-4770A>G) c.79-4770A>G (n.79-4770A>G) | dbSNP |
14 | g.52322456C>A | CA2541931286 | PTGER2 | c.844-4765C>A (n.844-4765C>A) c.79-4765C>A (n.79-4765C>A) | |
14 | g.52322461G>A | CA2137042311 | PTGER2 | c.844-4760G>A (n.844-4760G>A) c.79-4760G>A (n.79-4760G>A) | dbSNP |
14 | g.52322461G= | CA2137042310 | PTGER2 | c.844-4760G= (n.844-4760G=) c.79-4760G= (n.79-4760G=) | |
14 | g.52322464A>G | CA2510661950 | PTGER2 | c.844-4757A>G (n.844-4757A>G) c.79-4757A>G (n.79-4757A>G) | |
14 | g.52322466A= | CA2137042312 | PTGER2 | c.844-4755A= (n.844-4755A=) c.79-4755A= (n.79-4755A=) | |
14 | g.52322466A>C | CA2137042315 | PTGER2 | c.844-4755A>C (n.844-4755A>C) c.79-4755A>C (n.79-4755A>C) | dbSNP |