Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128848053A= | CA1742589581 | FLNC | c.4565A= (p.Gln1522=) | |
7 | g.128848053A>C | CA369202025 | FLNC | c.4565A>C (p.Gln1522Pro) | |
7 | g.128848053A>G | CA166183552 | FLNC | c.4565A>G (p.Gln1522Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128848053A>T | CA369202026 | FLNC | c.4565A>T (p.Gln1522Leu) | gnomAD v4 |
7 | g.128848054G>A | CA457848784 | FLNC | c.4566G>A (p.Gln1522=) | |
7 | g.128848054G>C | CA369202027 | FLNC | c.4566G>C (p.Gln1522His) | |
7 | g.128848054G= | CA1742589583 | FLNC | c.4566G= (p.Gln1522=) | |
7 | g.128848054G>T | CA4475377 | FLNC | c.4566G>T (p.Gln1522His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128848055G>A | CA369202028 | FLNC | c.4567G>A (p.Glu1523Lys) | gnomAD v4 |
7 | g.128848055G>C | CA369202029 | FLNC | c.4567G>C (p.Glu1523Gln) | |
7 | g.128848055G>T | CA369202030 | FLNC | c.4567G>T (p.Glu1523Ter) | gnomAD v4 |
7 | g.128848056A>C | CA369202031 | FLNC | c.4568A>C (p.Glu1523Ala) | |
7 | g.128848056A>G | CA369202032 | FLNC | c.4568A>G (p.Glu1523Gly) | COSMIC |
7 | g.128848056A>T | CA369202033 | FLNC | c.4568A>T (p.Glu1523Val) | |
7 | g.128848057G>A | CA457848793 | FLNC | c.4569G>A (p.Glu1523=) | |
7 | g.128848057G>C | CA369202034 | FLNC | c.4569G>C (p.Glu1523Asp) | |
7 | g.128848057G= | CA1742589585 | FLNC | c.4569G= (p.Glu1523=) | |
7 | g.128848057G>T | CA369202035 | FLNC | c.4569G>T (p.Glu1523Asp) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128848058G>A | CA369202036 | FLNC | c.4570G>A (p.Val1524Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128848058G>C | CA369202037 | FLNC | c.4570G>C (p.Val1524Leu) | |
7 | g.128848058G= | CA1742589587 | FLNC | c.4570G= (p.Val1524=) | |
7 | g.128848058G>T | CA369202038 | FLNC | c.4570G>T (p.Val1524Leu) | dbSNP gnomAD v4 |
7 | g.128848059T>A | CA369202039 | FLNC | c.4571T>A (p.Val1524Glu) | |
7 | g.128848059T>C | CA369202040 | FLNC | c.4571T>C (p.Val1524Ala) | gnomAD v4 |
7 | g.128848059T>G | CA369202041 | FLNC | c.4571T>G (p.Val1524Gly) | dbSNP |
7 | g.128848059T= | CA1742589589 | FLNC | c.4571T= (p.Val1524=) | |
7 | g.128848060G>A | CA457848802 | FLNC | c.4572G>A (p.Val1524=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128848060G>C | CA457848803 | FLNC | c.4572G>C (p.Val1524=) | |
7 | g.128848060G= | CA1742589591 | FLNC | c.4572G= (p.Val1524=) | |
7 | g.128848060G>T | CA457848804 | FLNC | c.4572G>T (p.Val1524=) | COSMIC |
7 | g.128848061C>A | CA369202042 | FLNC | c.4573C>A (p.Pro1525Thr) | gnomAD v4 |
7 | g.128848061C>G | CA369202043 | FLNC | c.4573C>G (p.Pro1525Ala) | |
7 | g.128848061C>T | CA369202044 | FLNC | c.4573C>T (p.Pro1525Ser) | gnomAD v4 |
7 | g.128848062C>A | CA369202045 | FLNC | c.4574C>A (p.Pro1525Gln) | COSMIC |
7 | g.128848062C>G | CA369202046 | FLNC | c.4574C>G (p.Pro1525Arg) | |
7 | g.128848062C>T | CA369202047 | FLNC | c.4574C>T (p.Pro1525Leu) | |
7 | g.128848063A>C | CA457848814 | FLNC | c.4575A>C (p.Pro1525=) | |
7 | g.128848063A>G | CA457848815 | FLNC | c.4575A>G (p.Pro1525=) | ClinVar |
7 | g.128848063A>T | CA457848816 | FLNC | c.4575A>T (p.Pro1525=) | |
7 | g.128848064C>A | CA369202048 | FLNC | c.4576C>A (p.Arg1526Ser) | |
7 | g.128848064C= | CA1742589594 | FLNC | c.4576C= (p.Arg1526=) | |
7 | g.128848064C>G | CA369202049 | FLNC | c.4576C>G (p.Arg1526Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128848064C>T | CA4475378 | FLNC | c.4576C>T (p.Arg1526Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128848065G>A | CA4475379 | FLNC | c.4577G>A (p.Arg1526His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128848065G>C | CA369202050 | FLNC | c.4577G>C (p.Arg1526Pro) | ClinVar |
7 | g.128848065G= | CA1742589599 | FLNC | c.4577G= (p.Arg1526=) | |
7 | g.128848065G>T | CA369202051 | FLNC | c.4577G>T (p.Arg1526Leu) | gnomAD v4 |
7 | g.128848066C>A | CA457848824 | FLNC | c.4578C>A (p.Arg1526=) | ClinVar gnomAD v4 |
7 | g.128848066C= | CA1742589602 | FLNC | c.4578C= (p.Arg1526=) | |
7 | g.128848066C>G | CA4475380 | FLNC | c.4578C>G (p.Arg1526=) | dbSNP ExAC gnomAD v2 gnomAD v4 |