Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128851588C>A | CA369208507 | FLNC,FLNC-AS1 | c.5802C>A (p.Asp1934Glu) c.5703C>A (p.Asp1901Glu) n.216-88G>T | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128851588C= | CA1742571617 | FLNC,FLNC-AS1 | c.5802C= (p.Asp1934=) c.5703C= (p.Asp1901=) n.216-88G= | |
7 | g.128851588C>G | CA4475791 | FLNC,FLNC-AS1 | c.5802C>G (p.Asp1934Glu) c.5703C>G (p.Asp1901Glu) n.216-88G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128851588C>T | CA457849250 | FLNC,FLNC-AS1 | c.5802C>T (p.Asp1934=) c.5703C>T (p.Asp1901=) n.216-88G>A | ClinVar |
7 | g.128851589A= | CA1742571641 | FLNC,FLNC-AS1 | c.5803A= (p.Lys1935=) c.5704A= (p.Lys1902=) n.216-89T= | |
7 | g.128851589A>C | CA369208514 | FLNC,FLNC-AS1 | c.5803A>C (p.Lys1935Gln) c.5704A>C (p.Lys1902Gln) n.216-89T>G | |
7 | g.128851589A>G | CA369208513 | FLNC,FLNC-AS1 | c.5803A>G (p.Lys1935Glu) c.5704A>G (p.Lys1902Glu) n.216-89T>C | ClinVar dbSNP gnomAD v4 |
7 | g.128851589A>T | CA369208511 | FLNC,FLNC-AS1 | c.5803A>T (p.Lys1935Ter) c.5704A>T (p.Lys1902Ter) n.216-89T>A | |
7 | g.128851590A>C | CA369208517 | FLNC,FLNC-AS1 | c.5804A>C (p.Lys1935Thr) c.5705A>C (p.Lys1902Thr) n.216-90T>G | |
7 | g.128851590A>G | CA369208520 | FLNC,FLNC-AS1 | c.5804A>G (p.Lys1935Arg) c.5705A>G (p.Lys1902Arg) n.216-90T>C | |
7 | g.128851590A>T | CA369208519 | FLNC,FLNC-AS1 | c.5804A>T (p.Lys1935Met) c.5705A>T (p.Lys1902Met) n.216-90T>A | |
7 | g.128851591G>A | CA4475792 | FLNC,FLNC-AS1 | c.5805G>A (p.Lys1935=) c.5706G>A (p.Lys1902=) n.216-91C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128851591G>C | CA369208524 | FLNC,FLNC-AS1 | c.5805G>C (p.Lys1935Asn) c.5706G>C (p.Lys1902Asn) n.216-91C>G | |
7 | g.128851591G= | CA1742571649 | FLNC,FLNC-AS1 | c.5805G= (p.Lys1935=) c.5706G= (p.Lys1902=) n.216-91C= | |
7 | g.128851591G>T | CA369208522 | FLNC,FLNC-AS1 | c.5805G>T (p.Lys1935Asn) c.5706G>T (p.Lys1902Asn) n.216-91C>A | |
7 | g.128851592C>A | CA369208526 | FLNC,FLNC-AS1 | c.5806C>A (p.His1936Asn) c.5707C>A (p.His1903Asn) n.216-92G>T | |
7 | g.128851592C>G | CA369208529 | FLNC,FLNC-AS1 | c.5806C>G (p.His1936Asp) c.5707C>G (p.His1903Asp) n.216-92G>C | |
7 | g.128851592C>T | CA369208527 | FLNC,FLNC-AS1 | c.5806C>T (p.His1936Tyr) c.5707C>T (p.His1903Tyr) n.216-92G>A | |
7 | g.128851593A= | CA1742571660 | FLNC,FLNC-AS1 | c.5807A= (p.His1936=) c.5708A= (p.His1903=) n.216-93T= | |
7 | g.128851593A>C | CA369208531 | FLNC,FLNC-AS1 | c.5807A>C (p.His1936Pro) c.5708A>C (p.His1903Pro) n.216-93T>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128851593A>G | CA369208535 | FLNC,FLNC-AS1 | c.5807A>G (p.His1936Arg) c.5708A>G (p.His1903Arg) n.216-93T>C | |
7 | g.128851593A>T | CA369208533 | FLNC,FLNC-AS1 | c.5807A>T (p.His1936Leu) c.5708A>T (p.His1903Leu) n.216-93T>A | |
7 | g.128851594C>A | CA369208538 | FLNC,FLNC-AS1 | c.5808C>A (p.His1936Gln) c.5709C>A (p.His1903Gln) n.216-94G>T | |
7 | g.128851594C>G | CA369208539 | FLNC,FLNC-AS1 | c.5808C>G (p.His1936Gln) c.5709C>G (p.His1903Gln) n.216-94G>C | |
7 | g.128851594C>T | CA457849265 | FLNC,FLNC-AS1 | c.5808C>T (p.His1936=) c.5709C>T (p.His1903=) n.216-94G>A | ClinVar dbSNP |
7 | g.128851595A>C | CA369208542 | FLNC,FLNC-AS1 | c.5809A>C (p.Ile1937Leu) c.5710A>C (p.Ile1904Leu) n.216-95T>G | |
7 | g.128851595A>G | CA369208544 | FLNC,FLNC-AS1 | c.5809A>G (p.Ile1937Val) c.5710A>G (p.Ile1904Val) n.216-95T>C | gnomAD v4 |
7 | g.128851595A>T | CA369208546 | FLNC,FLNC-AS1 | c.5809A>T (p.Ile1937Phe) c.5710A>T (p.Ile1904Phe) n.216-95T>A | |
7 | g.128851596T>A | CA369208548 | FLNC,FLNC-AS1 | c.5810T>A (p.Ile1937Asn) c.5711T>A (p.Ile1904Asn) n.216-96A>T | ClinVar dbSNP |
7 | g.128851596T>C | CA369208550 | FLNC,FLNC-AS1 | c.5810T>C (p.Ile1937Thr) c.5711T>C (p.Ile1904Thr) n.216-96A>G | |
7 | g.128851596T>G | CA369208552 | FLNC,FLNC-AS1 | c.5810T>G (p.Ile1937Ser) c.5711T>G (p.Ile1904Ser) n.216-96A>C | |
7 | g.128851596T= | CA1742571666 | FLNC,FLNC-AS1 | c.5810T= (p.Ile1937=) c.5711T= (p.Ile1904=) n.216-96A= | |
7 | g.128851597C>A | CA457849272 | FLNC,FLNC-AS1 | c.5811C>A (p.Ile1937=) c.5712C>A (p.Ile1904=) n.216-97G>T | |
7 | g.128851597C>G | CA369208554 | FLNC,FLNC-AS1 | c.5811C>G (p.Ile1937Met) c.5712C>G (p.Ile1904Met) n.216-97G>C | |
7 | g.128851597C>T | CA457849273 | FLNC,FLNC-AS1 | c.5811C>T (p.Ile1937=) c.5712C>T (p.Ile1904=) n.216-97G>A | |
7 | g.128851598C>A | CA369208557 | FLNC,FLNC-AS1 | c.5812C>A (p.Pro1938Thr) c.5713C>A (p.Pro1905Thr) n.216-98G>T | |
7 | g.128851598C>G | CA369208559 | FLNC,FLNC-AS1 | c.5812C>G (p.Pro1938Ala) c.5713C>G (p.Pro1905Ala) n.216-98G>C | |
7 | g.128851598C>T | CA369208561 | FLNC,FLNC-AS1 | c.5812C>T (p.Pro1938Ser) c.5713C>T (p.Pro1905Ser) n.216-98G>A | COSMIC |
7 | g.128851599C>A | CA369208567 | FLNC,FLNC-AS1 | c.5813C>A (p.Pro1938Gln) c.5714C>A (p.Pro1905Gln) n.216-99G>T | |
7 | g.128851599C= | CA1742571682 | FLNC,FLNC-AS1 | c.5813C= (p.Pro1938=) c.5714C= (p.Pro1905=) n.216-99G= | |
7 | g.128851599C>G | CA4475793 | FLNC,FLNC-AS1 | c.5813C>G (p.Pro1938Arg) c.5714C>G (p.Pro1905Arg) n.216-99G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128851599C>T | CA369208563 | FLNC,FLNC-AS1 | c.5813C>T (p.Pro1938Leu) c.5714C>T (p.Pro1905Leu) n.216-99G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
7 | g.128851600G>A | CA4475794 | FLNC,FLNC-AS1 | c.5814G>A (p.Pro1938=) c.5715G>A (p.Pro1905=) n.216-100C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128851600G>C | CA457849281 | FLNC,FLNC-AS1 | c.5814G>C (p.Pro1938=) c.5715G>C (p.Pro1905=) n.216-100C>G | ClinVar dbSNP |
7 | g.128851600G= | CA1742571692 | FLNC,FLNC-AS1 | c.5814G= (p.Pro1938=) c.5715G= (p.Pro1905=) n.216-100C= | |
7 | g.128851600G>T | CA457849283 | FLNC,FLNC-AS1 | c.5814G>T (p.Pro1938=) c.5715G>T (p.Pro1905=) n.216-100C>A | gnomAD v4 |
7 | g.128851603dup | CA166189098 | FLNC,FLNC-AS1 | c.5817dup (p.Ser1940GlufsTer10) c.5718dup (p.Ser1907GlufsTer10) n.216-100dup | dbSNP |
7 | g.128851603del | CA2684812617 | FLNC,FLNC-AS1 | c.5817del (p.Ser1940AlafsTer13) c.5718del (p.Ser1907AlafsTer13) n.216-100del | gnomAD v4 |
7 | g.128851601G>A | CA369208570 | FLNC,FLNC-AS1 | c.5815G>A (p.Gly1939Arg) c.5716G>A (p.Gly1906Arg) n.216-101C>T | |
7 | g.128851601G>C | CA369208572 | FLNC,FLNC-AS1 | c.5815G>C (p.Gly1939Arg) c.5716G>C (p.Gly1906Arg) n.216-101C>G |