Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128849388C>A | CA369203982 | FLNC | c.5009C>A (p.Ala1670Asp) | |
7 | g.128849388C>G | CA369203983 | FLNC | c.5009C>G (p.Ala1670Gly) | |
7 | g.128849388C>T | CA369203984 | FLNC | c.5009C>T (p.Ala1670Val) | |
7 | g.128849389C>A | CA457849052 | FLNC | c.5010C>A (p.Ala1670=) | |
7 | g.128849389C>G | CA457849054 | FLNC | c.5010C>G (p.Ala1670=) | |
7 | g.128849389C>T | CA457849056 | FLNC | c.5010C>T (p.Ala1670=) | |
7 | g.128849390A= | CA1742564319 | FLNC | c.5011A= (p.Lys1671=) | |
7 | g.128849390A>C | CA369203985 | FLNC | c.5011A>C (p.Lys1671Gln) | |
7 | g.128849390A>G | CA369203986 | FLNC | c.5011A>G (p.Lys1671Glu) | ClinVar dbSNP gnomAD v4 |
7 | g.128849390A>T | CA369203987 | FLNC | c.5011A>T (p.Lys1671Ter) | gnomAD v4 |
7 | g.128849391A>C | CA369203988 | FLNC | c.5012A>C (p.Lys1671Thr) | |
7 | g.128849391A>G | CA369203989 | FLNC | c.5012A>G (p.Lys1671Arg) | |
7 | g.128849391A>T | CA369203990 | FLNC | c.5012A>T (p.Lys1671Met) | |
7 | g.128849392G>A | CA457849066 | FLNC | c.5013G>A (p.Lys1671=) | |
7 | g.128849392G>C | CA369203991 | FLNC | c.5013G>C (p.Lys1671Asn) | |
7 | g.128849392G= | CA1742564325 | FLNC | c.5013G= (p.Lys1671=) | |
7 | g.128849392G>T | CA4475542 | FLNC | c.5013G>T (p.Lys1671Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849393G>A | CA4475543 | FLNC | c.5014G>A (p.Ala1672Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128849393G>C | CA369203992 | FLNC | c.5014G>C (p.Ala1672Pro) | |
7 | g.128849393G= | CA1742564328 | FLNC | c.5014G= (p.Ala1672=) | |
7 | g.128849393G>T | CA369203993 | FLNC | c.5014G>T (p.Ala1672Ser) | |
7 | g.128849394C>A | CA369203994 | FLNC | c.5015C>A (p.Ala1672Glu) | |
7 | g.128849394C>G | CA369203995 | FLNC | c.5015C>G (p.Ala1672Gly) | |
7 | g.128849394C>T | CA369203996 | FLNC | c.5015C>T (p.Ala1672Val) | |
7 | g.128849395A>C | CA457848798 | FLNC | c.5016A>C (p.Ala1672=) | |
7 | g.128849395A>G | CA457848799 | FLNC | c.5016A>G (p.Ala1672=) | |
7 | g.128849395A>T | CA457848800 | FLNC | c.5016A>T (p.Ala1672=) | |
7 | g.128849396G>A | CA369203997 | FLNC | c.5017G>A (p.Ala1673Thr) | |
7 | g.128849396G>C | CA369203998 | FLNC | c.5017G>C (p.Ala1673Pro) | |
7 | g.128849396G>T | CA369203999 | FLNC | c.5017G>T (p.Ala1673Ser) | |
7 | g.128849397C>A | CA369204000 | FLNC | c.5018C>A (p.Ala1673Asp) | |
7 | g.128849397C>G | CA369204001 | FLNC | c.5018C>G (p.Ala1673Gly) | |
7 | g.128849397C>T | CA369204002 | FLNC | c.5018C>T (p.Ala1673Val) | COSMIC |
7 | g.128849398C>A | CA457848807 | FLNC | c.5019C>A (p.Ala1673=) | ClinVar gnomAD v4 |
7 | g.128849398C= | CA1742564332 | FLNC | c.5019C= (p.Ala1673=) | |
7 | g.128849398C>G | CA457848808 | FLNC | c.5019C>G (p.Ala1673=) | |
7 | g.128849398C>T | CA4475544 | FLNC | c.5019C>T (p.Ala1673=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849399G>A | CA4475545 | FLNC | c.5020G>A (p.Gly1674Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849399G>C | CA369204004 | FLNC | c.5020G>C (p.Gly1674Arg) | |
7 | g.128849399G= | CA1742564338 | FLNC | c.5020G= (p.Gly1674=) | |
7 | g.128849399G>T | CA369204003 | FLNC | c.5020G>T (p.Gly1674Cys) | |
7 | g.128849400_128849402del | CA2580076543 | FLNC | c.5021_5023del (p.Gly1674del) | ClinVar |
7 | g.128849400G>A | CA369204005 | FLNC | c.5021G>A (p.Gly1674Asp) | |
7 | g.128849400G>C | CA369204006 | FLNC | c.5021G>C (p.Gly1674Ala) | |
7 | g.128849400G>T | CA369204007 | FLNC | c.5021G>T (p.Gly1674Val) | |
7 | g.128849401T>A | CA457848818 | FLNC | c.5022T>A (p.Gly1674=) | gnomAD v4 |
7 | g.128849401T>C | CA457848819 | FLNC | c.5022T>C (p.Gly1674=) | |
7 | g.128849401T>G | CA457848820 | FLNC | c.5022T>G (p.Gly1674=) | ClinVar dbSNP |
7 | g.128849401T= | CA1742564355 | FLNC | c.5022T= (p.Gly1674=) | |
7 | g.128849402G>A | CA369204008 | FLNC | c.5023G>A (p.Glu1675Lys) |