Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.169529635C>A | CA343129413 | F5 | c.5392G>T (p.Glu1798Ter) c.5407G>T (p.Glu1803Ter) c.4981G>T (p.Glu1661Ter) | |
1 | g.169529635C= | CA1144229041 | F5 | c.5392G= (p.Glu1798=) c.5407G= (p.Glu1803=) c.4981G= (p.Glu1661=) | |
1 | g.169529635C>G | CA343129438 | F5 | c.5392G>C (p.Glu1798Gln) c.5407G>C (p.Glu1803Gln) c.4981G>C (p.Glu1661Gln) | gnomAD v4 |
1 | g.169529635C>T | CA215971 | F5 | c.5392G>A (p.Glu1798Lys) c.5407G>A (p.Glu1803Lys) c.4981G>A (p.Glu1661Lys) | ClinVar dbSNP |
1 | g.169529636T>A | CA421737410 | F5 | c.5391A>T (p.Ser1797=) c.5406A>T (p.Ser1802=) c.4980A>T (p.Ser1660=) | |
1 | g.169529636T>C | CA421737412 | F5 | c.5391A>G (p.Ser1797=) c.5406A>G (p.Ser1802=) c.4980A>G (p.Ser1660=) | |
1 | g.169529636T>G | CA421737414 | F5 | c.5391A>C (p.Ser1797=) c.5406A>C (p.Ser1802=) c.4980A>C (p.Ser1660=) | |
1 | g.169529637G>A | CA343129440 | F5 | c.5390C>T (p.Ser1797Leu) c.5405C>T (p.Ser1802Leu) c.4979C>T (p.Ser1660Leu) | |
1 | g.169529637G>C | CA343129444 | F5 | c.5390C>G (p.Ser1797Ter) c.5405C>G (p.Ser1802Ter) c.4979C>G (p.Ser1660Ter) | |
1 | g.169529637G>T | CA343129446 | F5 | c.5390C>A (p.Ser1797Ter) c.5405C>A (p.Ser1802Ter) c.4979C>A (p.Ser1660Ter) | |
1 | g.169529638A>C | CA343129448 | F5 | c.5389T>G (p.Ser1797Ala) c.5404T>G (p.Ser1802Ala) c.4978T>G (p.Ser1660Ala) | |
1 | g.169529638A>G | CA343129453 | F5 | c.5389T>C (p.Ser1797Pro) c.5404T>C (p.Ser1802Pro) c.4978T>C (p.Ser1660Pro) | |
1 | g.169529638A>T | CA343129467 | F5 | c.5389T>A (p.Ser1797Thr) c.5404T>A (p.Ser1802Thr) c.4978T>A (p.Ser1660Thr) | |
1 | g.169529639G>A | CA421737427 | F5 | c.5388C>T (p.Ser1796=) c.5403C>T (p.Ser1801=) c.4977C>T (p.Ser1659=) | |
1 | g.169529639G>C | CA421737431 | F5 | c.5388C>G (p.Ser1796=) c.5403C>G (p.Ser1801=) c.4977C>G (p.Ser1659=) | |
1 | g.169529639G>T | CA421737428 | F5 | c.5388C>A (p.Ser1796=) c.5403C>A (p.Ser1801=) c.4977C>A (p.Ser1659=) | |
1 | g.169529640G>A | CA343129475 | F5 | c.5387C>T (p.Ser1796Phe) c.5402C>T (p.Ser1801Phe) c.4976C>T (p.Ser1659Phe) | dbSNP gnomAD v4 |
1 | g.169529640G>C | CA343129468 | F5 | c.5387C>G (p.Ser1796Cys) c.5402C>G (p.Ser1801Cys) c.4976C>G (p.Ser1659Cys) | |
1 | g.169529640G= | CA1206135810 | F5 | c.5387C= (p.Ser1796=) c.5402C= (p.Ser1801=) c.4976C= (p.Ser1659=) | |
1 | g.169529640G>T | CA343129469 | F5 | c.5387C>A (p.Ser1796Tyr) c.5402C>A (p.Ser1801Tyr) c.4976C>A (p.Ser1659Tyr) | |
1 | g.169529641A= | CA1206135811 | F5 | c.5386T= (p.Ser1796=) c.5401T= (p.Ser1801=) c.4975T= (p.Ser1659=) | |
1 | g.169529641A>C | CA343129479 | F5 | c.5386T>G (p.Ser1796Ala) c.5401T>G (p.Ser1801Ala) c.4975T>G (p.Ser1659Ala) | gnomAD v4 |
1 | g.169529641A>G | CA343129481 | F5 | c.5386T>C (p.Ser1796Pro) c.5401T>C (p.Ser1801Pro) c.4975T>C (p.Ser1659Pro) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.169529641A>T | CA343129480 | F5 | c.5386T>A (p.Ser1796Thr) c.5401T>A (p.Ser1801Thr) c.4975T>A (p.Ser1659Thr) | gnomAD v4 |
1 | g.169529642T>A | CA421737440 | F5 | c.5385A>T (p.Thr1795=) c.5400A>T (p.Thr1800=) c.4974A>T (p.Thr1658=) | |
1 | g.169529642T>C | CA421737442 | F5 | c.5385A>G (p.Thr1795=) c.5400A>G (p.Thr1800=) c.4974A>G (p.Thr1658=) | |
1 | g.169529642T>G | CA421737444 | F5 | c.5385A>C (p.Thr1795=) c.5400A>C (p.Thr1800=) c.4974A>C (p.Thr1658=) | |
1 | g.169529643G>A | CA343129485 | F5 | c.5384C>T (p.Thr1795Ile) c.5399C>T (p.Thr1800Ile) c.4973C>T (p.Thr1658Ile) | |
1 | g.169529643G>C | CA343129491 | F5 | c.5384C>G (p.Thr1795Arg) c.5399C>G (p.Thr1800Arg) c.4973C>G (p.Thr1658Arg) | |
1 | g.169529643G>T | CA343129496 | F5 | c.5384C>A (p.Thr1795Lys) c.5399C>A (p.Thr1800Lys) c.4973C>A (p.Thr1658Lys) | |
1 | g.169529644T>A | CA343129501 | F5 | c.5383A>T (p.Thr1795Ser) c.5398A>T (p.Thr1800Ser) c.4972A>T (p.Thr1658Ser) | |
1 | g.169529644T>C | CA343129506 | F5 | c.5383A>G (p.Thr1795Ala) c.5398A>G (p.Thr1800Ala) c.4972A>G (p.Thr1658Ala) | |
1 | g.169529644T>G | CA1233516 | F5 | c.5383A>C (p.Thr1795Pro) c.5398A>C (p.Thr1800Pro) c.4972A>C (p.Thr1658Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.169529644T= | CA1147202499 | F5 | c.5383A= (p.Thr1795=) c.5398A= (p.Thr1800=) c.4972A= (p.Thr1658=) | |
1 | g.169529645G>A | CA421737457 | F5 | c.5382C>T (p.Leu1794=) c.5397C>T (p.Leu1799=) c.4971C>T (p.Leu1657=) | |
1 | g.169529645G>C | CA421737459 | F5 | c.5382C>G (p.Leu1794=) c.5397C>G (p.Leu1799=) c.4971C>G (p.Leu1657=) | |
1 | g.169529645G>T | CA421737462 | F5 | c.5382C>A (p.Leu1794=) c.5397C>A (p.Leu1799=) c.4971C>A (p.Leu1657=) | |
1 | g.169529646A= | CA1206135812 | F5 | c.5381T= (p.Leu1794=) c.5396T= (p.Leu1799=) c.4970T= (p.Leu1657=) | |
1 | g.169529646A>C | CA343129517 | F5 | c.5381T>G (p.Leu1794Arg) c.5396T>G (p.Leu1799Arg) c.4970T>G (p.Leu1657Arg) | |
1 | g.169529646A>G | CA343129526 | F5 | c.5381T>C (p.Leu1794Pro) c.5396T>C (p.Leu1799Pro) c.4970T>C (p.Leu1657Pro) | |
1 | g.169529646A>T | CA343129532 | F5 | c.5381T>A (p.Leu1794His) c.5396T>A (p.Leu1799His) c.4970T>A (p.Leu1657His) | dbSNP |
1 | g.169529647G>A | CA343129535 | F5 | c.5380C>T (p.Leu1794Phe) c.5395C>T (p.Leu1799Phe) c.4969C>T (p.Leu1657Phe) | |
1 | g.169529647G>C | CA343129537 | F5 | c.5380C>G (p.Leu1794Val) c.5395C>G (p.Leu1799Val) c.4969C>G (p.Leu1657Val) | |
1 | g.169529647G>T | CA343129538 | F5 | c.5380C>A (p.Leu1794Ile) c.5395C>A (p.Leu1799Ile) c.4969C>A (p.Leu1657Ile) | |
1 | g.169529648T>A | CA343129542 | F5 | c.5379A>T (p.Arg1793Ser) c.5394A>T (p.Arg1798Ser) c.4968A>T (p.Arg1656Ser) | |
1 | g.169529648T>C | CA421737474 | F5 | c.5379A>G (p.Arg1793=) c.5394A>G (p.Arg1798=) c.4968A>G (p.Arg1656=) | |
1 | g.169529648T>G | CA343129541 | F5 | c.5379A>C (p.Arg1793Ser) c.5394A>C (p.Arg1798Ser) c.4968A>C (p.Arg1656Ser) | |
1 | g.169529649C>A | CA343129543 | F5 | c.5378G>T (p.Arg1793Ile) c.5393G>T (p.Arg1798Ile) c.4967G>T (p.Arg1656Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.169529649C= | CA1206135813 | F5 | c.5378G= (p.Arg1793=) c.5393G= (p.Arg1798=) c.4967G= (p.Arg1656=) | |
1 | g.169529649C>G | CA343129545 | F5 | c.5378G>C (p.Arg1793Thr) c.5393G>C (p.Arg1798Thr) c.4967G>C (p.Arg1656Thr) | COSMIC |