Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128845243G>A | CA4475121 | FLNC | c.3778G>A (p.Val1260Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128845243G>C | CA369198046 | FLNC | c.3778G>C (p.Val1260Leu) | |
7 | g.128845243G= | CA1742585465 | FLNC | c.3778G= (p.Val1260=) | |
7 | g.128845243G>T | CA369198047 | FLNC | c.3778G>T (p.Val1260Phe) | |
7 | g.128845244T>A | CA369198052 | FLNC | c.3779T>A (p.Val1260Asp) | |
7 | g.128845244T>C | CA369198056 | FLNC | c.3779T>C (p.Val1260Ala) | |
7 | g.128845244T>G | CA369198058 | FLNC | c.3779T>G (p.Val1260Gly) | |
7 | g.128845245T>A | CA457579428 | FLNC | c.3780T>A (p.Val1260=) | |
7 | g.128845245T>C | CA457579429 | FLNC | c.3780T>C (p.Val1260=) | |
7 | g.128845245T>G | CA457579431 | FLNC | c.3780T>G (p.Val1260=) | |
7 | g.128845246G>A | CA4475122 | FLNC | c.3781G>A (p.Glu1261Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128845246G>C | CA369198063 | FLNC | c.3781G>C (p.Glu1261Gln) | ClinVar dbSNP gnomAD v4 |
7 | g.128845246G= | CA1742585470 | FLNC | c.3781G= (p.Glu1261=) | |
7 | g.128845246G>T | CA369198066 | FLNC | c.3781G>T (p.Glu1261Ter) | |
7 | g.128845247A>C | CA369198068 | FLNC | c.3782A>C (p.Glu1261Ala) | |
7 | g.128845247A>G | CA369198071 | FLNC | c.3782A>G (p.Glu1261Gly) | |
7 | g.128845247A>T | CA369198074 | FLNC | c.3782A>T (p.Glu1261Val) | |
7 | g.128845248G>A | CA457579449 | FLNC | c.3783G>A (p.Glu1261=) | ClinVar dbSNP |
7 | g.128845248G>C | CA369198079 | FLNC | c.3783G>C (p.Glu1261Asp) | |
7 | g.128845248G= | CA1742585480 | FLNC | c.3783G= (p.Glu1261=) | |
7 | g.128845248G>T | CA369198082 | FLNC | c.3783G>T (p.Glu1261Asp) | |
7 | g.128845249C>A | CA369198092 | FLNC | c.3784C>A (p.Pro1262Thr) | |
7 | g.128845249C>G | CA369198089 | FLNC | c.3784C>G (p.Pro1262Ala) | |
7 | g.128845249C>T | CA369198086 | FLNC | c.3784C>T (p.Pro1262Ser) | gnomAD v4 |
7 | g.128845250C>A | CA369198096 | FLNC | c.3785C>A (p.Pro1262Gln) | |
7 | g.128845250C= | CA1742585485 | FLNC | c.3785C= (p.Pro1262=) | |
7 | g.128845250C>G | CA369198100 | FLNC | c.3785C>G (p.Pro1262Arg) | |
7 | g.128845250C>T | CA4475123 | FLNC | c.3785C>T (p.Pro1262Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128845251A= | CA1742585489 | FLNC | c.3786A= (p.Pro1262=) | |
7 | g.128845251A>C | CA457579468 | FLNC | c.3786A>C (p.Pro1262=) | |
7 | g.128845251A>G | CA457579469 | FLNC | c.3786A>G (p.Pro1262=) | dbSNP |
7 | g.128845251A>T | CA457579471 | FLNC | c.3786A>T (p.Pro1262=) | gnomAD v4 |
7 | g.128845252C>A | CA369198104 | FLNC | c.3787C>A (p.His1263Asn) | gnomAD v4 |
7 | g.128845252C>G | CA369198106 | FLNC | c.3787C>G (p.His1263Asp) | |
7 | g.128845252C>T | CA369198109 | FLNC | c.3787C>T (p.His1263Tyr) | |
7 | g.128845253A>C | CA369198113 | FLNC | c.3788A>C (p.His1263Pro) | |
7 | g.128845253A>G | CA369198115 | FLNC | c.3788A>G (p.His1263Arg) | |
7 | g.128845253A>T | CA369198118 | FLNC | c.3788A>T (p.His1263Leu) | |
7 | g.128845254C>A | CA369198124 | FLNC | c.3789C>A (p.His1263Gln) | gnomAD v4 |
7 | g.128845254C= | CA1742585494 | FLNC | c.3789C= (p.His1263=) | |
7 | g.128845254C>G | CA369198126 | FLNC | c.3789C>G (p.His1263Gln) | |
7 | g.128845254C>T | CA4475124 | FLNC | c.3789C>T (p.His1263=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128845255G>A | CA4475125 | FLNC | c.3790G>A (p.Gly1264Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128845255G>C | CA369198131 | FLNC | c.3790G>C (p.Gly1264Arg) | |
7 | g.128845255G= | CA1742585502 | FLNC | c.3790G= (p.Gly1264=) | |
7 | g.128845255G>T | CA369198133 | FLNC | c.3790G>T (p.Gly1264Cys) | ClinVar dbSNP |
7 | g.128845256G>A | CA369198149 | FLNC | c.3790+1G>A (n.3790+1G>A) | ClinVar dbSNP gnomAD v2 |
7 | g.128845256G>C | CA369198145 | FLNC | c.3790+1G>C (n.3790+1G>C) | ClinVar dbSNP |
7 | g.128845256G= | CA1742585509 | FLNC | c.3790+1G= (n.3790+1G=) | |
7 | g.128845256G>T | CA369198147 | FLNC | c.3790+1G>T (n.3790+1G>T) |