Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128851582C>A | CA369208478 | FLNC,FLNC-AS1 | c.5796C>A (p.Phe1932Leu) c.5697C>A (p.Phe1899Leu) n.216-82G>T | |
7 | g.128851582C= | CA1742571590 | FLNC,FLNC-AS1 | c.5796C= (p.Phe1932=) c.5697C= (p.Phe1899=) n.216-82G= | |
7 | g.128851582C>G | CA166189059 | FLNC,FLNC-AS1 | c.5796C>G (p.Phe1932Leu) c.5697C>G (p.Phe1899Leu) n.216-82G>C | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128851582C>T | CA4475788 | FLNC,FLNC-AS1 | c.5796C>T (p.Phe1932=) c.5697C>T (p.Phe1899=) n.216-82G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128851583G>A | CA4475790 | FLNC,FLNC-AS1 | c.5797G>A (p.Asp1933Asn) c.5698G>A (p.Asp1900Asn) n.216-83C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128851583G>C | CA369208483 | FLNC,FLNC-AS1 | c.5797G>C (p.Asp1933His) c.5698G>C (p.Asp1900His) n.216-83C>G | gnomAD v4 |
7 | g.128851583G= | CA1742571597 | FLNC,FLNC-AS1 | c.5797G= (p.Asp1933=) c.5698G= (p.Asp1900=) n.216-83C= | |
7 | g.128851583G>T | CA4475789 | FLNC,FLNC-AS1 | c.5797G>T (p.Asp1933Tyr) c.5698G>T (p.Asp1900Tyr) n.216-83C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128851584A>C | CA369208487 | FLNC,FLNC-AS1 | c.5798A>C (p.Asp1933Ala) c.5699A>C (p.Asp1900Ala) n.216-84T>G | |
7 | g.128851584A>G | CA369208490 | FLNC,FLNC-AS1 | c.5798A>G (p.Asp1933Gly) c.5699A>G (p.Asp1900Gly) n.216-84T>C | |
7 | g.128851584A>T | CA369208488 | FLNC,FLNC-AS1 | c.5798A>T (p.Asp1933Val) c.5699A>T (p.Asp1900Val) n.216-84T>A | |
7 | g.128851585T>A | CA369208492 | FLNC,FLNC-AS1 | c.5799T>A (p.Asp1933Glu) c.5700T>A (p.Asp1900Glu) n.216-85A>T | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128851585T>C | CA457849246 | FLNC,FLNC-AS1 | c.5799T>C (p.Asp1933=) c.5700T>C (p.Asp1900=) n.216-85A>G | |
7 | g.128851585T>G | CA369208494 | FLNC,FLNC-AS1 | c.5799T>G (p.Asp1933Glu) c.5700T>G (p.Asp1900Glu) n.216-85A>C | |
7 | g.128851585T= | CA1742571611 | FLNC,FLNC-AS1 | c.5799T= (p.Asp1933=) c.5700T= (p.Asp1900=) n.216-85A= | |
7 | g.128851586G>A | CA369208496 | FLNC,FLNC-AS1 | c.5800G>A (p.Asp1934Asn) c.5701G>A (p.Asp1901Asn) n.216-86C>T | |
7 | g.128851586G>C | CA369208498 | FLNC,FLNC-AS1 | c.5800G>C (p.Asp1934His) c.5701G>C (p.Asp1901His) n.216-86C>G | |
7 | g.128851586G>T | CA369208500 | FLNC,FLNC-AS1 | c.5800G>T (p.Asp1934Tyr) c.5701G>T (p.Asp1901Tyr) n.216-86C>A | |
7 | g.128851587A>C | CA369208502 | FLNC,FLNC-AS1 | c.5801A>C (p.Asp1934Ala) c.5702A>C (p.Asp1901Ala) n.216-87T>G | |
7 | g.128851587A>G | CA369208504 | FLNC,FLNC-AS1 | c.5801A>G (p.Asp1934Gly) c.5702A>G (p.Asp1901Gly) n.216-87T>C | gnomAD v4 |
7 | g.128851587A>T | CA369208505 | FLNC,FLNC-AS1 | c.5801A>T (p.Asp1934Val) c.5702A>T (p.Asp1901Val) n.216-87T>A | |
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 |