Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128849365G>A | CA457848996 | FLNC | c.4986G>A (p.Gln1662=) | |
7 | g.128849365G>C | CA369203933 | FLNC | c.4986G>C (p.Gln1662His) | |
7 | g.128849365G>T | CA369203934 | FLNC | c.4986G>T (p.Gln1662His) | |
7 | g.128849366G>A | CA369203937 | FLNC | c.4987G>A (p.Glu1663Lys) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128849366G>C | CA369203935 | FLNC | c.4987G>C (p.Glu1663Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849366G= | CA1742564168 | FLNC | c.4987G= (p.Glu1663=) | |
7 | g.128849366G>T | CA369203936 | FLNC | c.4987G>T (p.Glu1663Ter) | COSMIC |
7 | g.128849367A>C | CA369203938 | FLNC | c.4988A>C (p.Glu1663Ala) | |
7 | g.128849367A>G | CA369203939 | FLNC | c.4988A>G (p.Glu1663Gly) | ClinVar gnomAD v4 |
7 | g.128849367A>T | CA369203940 | FLNC | c.4988A>T (p.Glu1663Val) | |
7 | g.128849368G>A | CA457849000 | FLNC | c.4989G>A (p.Glu1663=) | ClinVar |
7 | g.128849368G>C | CA369203941 | FLNC | c.4989G>C (p.Glu1663Asp) | |
7 | g.128849368G= | CA1742564170 | FLNC | c.4989G= (p.Glu1663=) | |
7 | g.128849368G>T | CA166185374 | FLNC | c.4989G>T (p.Glu1663Asp) | dbSNP |
7 | g.128849369A>C | CA369203942 | FLNC | c.4990A>C (p.Thr1664Pro) | |
7 | g.128849369A>G | CA369203943 | FLNC | c.4990A>G (p.Thr1664Ala) | gnomAD v4 |
7 | g.128849369A>T | CA369203944 | FLNC | c.4990A>T (p.Thr1664Ser) | |
7 | g.128849370C>A | CA369203945 | FLNC | c.4991C>A (p.Thr1664Lys) | |
7 | g.128849370C= | CA1742564205 | FLNC | c.4991C= (p.Thr1664=) | |
7 | g.128849370C>G | CA369203946 | FLNC | c.4991C>G (p.Thr1664Arg) | |
7 | g.128849370C>T | CA4475536 | FLNC | c.4991C>T (p.Thr1664Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128849371G>A | CA4475537 | FLNC | c.4992G>A (p.Thr1664=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128849371G>C | CA457849005 | FLNC | c.4992G>C (p.Thr1664=) | |
7 | g.128849371G= | CA1742564212 | FLNC | c.4992G= (p.Thr1664=) | |
7 | g.128849371G>T | CA457849006 | FLNC | c.4992G>T (p.Thr1664=) | COSMIC |
7 | g.128849372G>A | CA369203947 | FLNC | c.4993G>A (p.Val1665Met) | gnomAD v4 |
7 | g.128849372G>C | CA369203948 | FLNC | c.4993G>C (p.Val1665Leu) | |
7 | g.128849372G>T | CA369203949 | FLNC | c.4993G>T (p.Val1665Leu) | |
7 | g.128849373T>A | CA369203950 | FLNC | c.4994T>A (p.Val1665Glu) | |
7 | g.128849373T>C | CA369203952 | FLNC | c.4994T>C (p.Val1665Ala) | COSMIC |
7 | g.128849373T>G | CA369203951 | FLNC | c.4994T>G (p.Val1665Gly) | dbSNP |
7 | g.128849373T= | CA1742564266 | FLNC | c.4994T= (p.Val1665=) | |
7 | g.128849374G>A | CA166185381 | FLNC | c.4995G>A (p.Val1665=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.128849374G>C | CA457849011 | FLNC | c.4995G>C (p.Val1665=) | |
7 | g.128849374G= | CA1742564274 | FLNC | c.4995G= (p.Val1665=) | |
7 | g.128849374G>T | CA457849012 | FLNC | c.4995G>T (p.Val1665=) | |
7 | g.128849375A= | CA1742564284 | FLNC | c.4996A= (p.Ile1666=) | |
7 | g.128849375A>C | CA369203953 | FLNC | c.4996A>C (p.Ile1666Leu) | |
7 | g.128849375A>G | CA369203954 | FLNC | c.4996A>G (p.Ile1666Val) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128849375A>T | CA369203955 | FLNC | c.4996A>T (p.Ile1666Phe) | |
7 | g.128849376T>A | CA369203956 | FLNC | c.4997T>A (p.Ile1666Asn) | |
7 | g.128849376T>C | CA369203957 | FLNC | c.4997T>C (p.Ile1666Thr) | |
7 | g.128849376T>G | CA369203958 | FLNC | c.4997T>G (p.Ile1666Ser) | |
7 | g.128849377C>A | CA457849017 | FLNC | c.4998C>A (p.Ile1666=) | |
7 | g.128849377C= | CA1742564289 | FLNC | c.4998C= (p.Ile1666=) | |
7 | g.128849377C>G | CA369203959 | FLNC | c.4998C>G (p.Ile1666Met) | dbSNP gnomAD v4 |
7 | g.128849377C>T | CA457849016 | FLNC | c.4998C>T (p.Ile1666=) | |
7 | g.128849378A>C | CA369203960 | FLNC | c.4999A>C (p.Thr1667Pro) | |
7 | g.128849378A>G | CA369203961 | FLNC | c.4999A>G (p.Thr1667Ala) | |
7 | g.128849378A>T | CA369203962 | FLNC | c.4999A>T (p.Thr1667Ser) |