Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128845140C>A | CA457578867 | FLNC | c.3675C>A (p.Thr1225=) | dbSNP gnomAD v2 |
7 | g.128845140C= | CA1742585154 | FLNC | c.3675C= (p.Thr1225=) | |
7 | g.128845140C>G | CA457578869 | FLNC | c.3675C>G (p.Thr1225=) | |
7 | g.128845140C>T | CA457578871 | FLNC | c.3675C>T (p.Thr1225=) | dbSNP |
7 | g.128845141A= | CA1742585157 | FLNC | c.3676A= (p.Ile1226=) | |
7 | g.128845141A>C | CA369197643 | FLNC | c.3676A>C (p.Ile1226Leu) | |
7 | g.128845141A>G | CA369197640 | FLNC | c.3676A>G (p.Ile1226Val) | ClinVar dbSNP gnomAD v4 |
7 | g.128845141A>T | CA369197642 | FLNC | c.3676A>T (p.Ile1226Phe) | |
7 | g.128845142T>A | CA369197645 | FLNC | c.3677T>A (p.Ile1226Asn) | |
7 | g.128845142T>C | CA369197647 | FLNC | c.3677T>C (p.Ile1226Thr) | |
7 | g.128845142T>G | CA369197649 | FLNC | c.3677T>G (p.Ile1226Ser) | |
7 | g.128845143T>A | CA457578877 | FLNC | c.3678T>A (p.Ile1226=) | |
7 | g.128845143T>C | CA457578879 | FLNC | c.3678T>C (p.Ile1226=) | |
7 | g.128845143T>G | CA369197651 | FLNC | c.3678T>G (p.Ile1226Met) | |
7 | g.128845143T= | CA1742585160 | FLNC | c.3678T= (p.Ile1226=) | |
7 | g.128845144A>C | CA369197658 | FLNC | c.3679A>C (p.Thr1227Pro) | |
7 | g.128845144A>G | CA369197655 | FLNC | c.3679A>G (p.Thr1227Ala) | |
7 | g.128845144A>T | CA369197654 | FLNC | c.3679A>T (p.Thr1227Ser) | |
7 | g.128845144dup | CA1107053651 | FLNC | c.3679dup (p.Thr1227AsnfsTer?) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128845145C>A | CA369197660 | FLNC | c.3680C>A (p.Thr1227Asn) | |
7 | g.128845145C= | CA1742585166 | FLNC | c.3680C= (p.Thr1227=) | |
7 | g.128845145C>G | CA369197661 | FLNC | c.3680C>G (p.Thr1227Ser) | |
7 | g.128845145C>T | CA4475098 | FLNC | c.3680C>T (p.Thr1227Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128845146C>A | CA457578892 | FLNC | c.3681C>A (p.Thr1227=) | |
7 | g.128845146C>G | CA457578890 | FLNC | c.3681C>G (p.Thr1227=) | |
7 | g.128845146C>T | CA457578889 | FLNC | c.3681C>T (p.Thr1227=) | |
7 | g.128845147A>C | CA369197664 | FLNC | c.3682A>C (p.Ile1228Leu) | gnomAD v4 |
7 | g.128845147A>G | CA369197666 | FLNC | c.3682A>G (p.Ile1228Val) | |
7 | g.128845147A>T | CA369197668 | FLNC | c.3682A>T (p.Ile1228Phe) | |
7 | g.128845148T>A | CA369197671 | FLNC | c.3683T>A (p.Ile1228Asn) | |
7 | g.128845148T>C | CA369197674 | FLNC | c.3683T>C (p.Ile1228Thr) | |
7 | g.128845148T>G | CA369197672 | FLNC | c.3683T>G (p.Ile1228Ser) | |
7 | g.128845149C>A | CA457578899 | FLNC | c.3684C>A (p.Ile1228=) | |
7 | g.128845149C>G | CA369197675 | FLNC | c.3684C>G (p.Ile1228Met) | |
7 | g.128845149C>T | CA457578902 | FLNC | c.3684C>T (p.Ile1228=) | gnomAD v4 |
7 | g.128845150A>C | CA369197677 | FLNC | c.3685A>C (p.Lys1229Gln) | COSMIC |
7 | g.128845150A>G | CA369197679 | FLNC | c.3685A>G (p.Lys1229Glu) | |
7 | g.128845150A>T | CA369197681 | FLNC | c.3685A>T (p.Lys1229Ter) | |
7 | g.128845151A>C | CA369197683 | FLNC | c.3686A>C (p.Lys1229Thr) | |
7 | g.128845151A>G | CA369197685 | FLNC | c.3686A>G (p.Lys1229Arg) | |
7 | g.128845151A>T | CA369197687 | FLNC | c.3686A>T (p.Lys1229Met) | |
7 | g.128845152G>A | CA457578909 | FLNC | c.3687G>A (p.Lys1229=) | ClinVar dbSNP |
7 | g.128845152G>C | CA369197689 | FLNC | c.3687G>C (p.Lys1229Asn) | |
7 | g.128845152G= | CA1742585178 | FLNC | c.3687G= (p.Lys1229=) | |
7 | g.128845152G>T | CA369197691 | FLNC | c.3687G>T (p.Lys1229Asn) | |
7 | g.128845153T>A | CA369197692 | FLNC | c.3688T>A (p.Tyr1230Asn) | |
7 | g.128845153T>C | CA369197694 | FLNC | c.3688T>C (p.Tyr1230His) | |
7 | g.128845153T>G | CA369197696 | FLNC | c.3688T>G (p.Tyr1230Asp) | |
7 | g.128845154A= | CA1742585188 | FLNC | c.3689A= (p.Tyr1230=) | |
7 | g.128845154A>C | CA369197698 | FLNC | c.3689A>C (p.Tyr1230Ser) | ClinVar |