Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128840123_128840136del | CA2695208476 | FLNC | c.1512_1525del (p.Gly505GlnfsTer?) | |
7 | g.128840123C>A | CA457582760 | FLNC | c.1512C>A (p.Ala504=) | |
7 | g.128840123C= | CA1742545934 | FLNC | c.1512C= (p.Ala504=) | |
7 | g.128840123C>G | CA457582757 | FLNC | c.1512C>G (p.Ala504=) | |
7 | g.128840123C>T | CA4474364 | FLNC | c.1512C>T (p.Ala504=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840126_128840131dup | CA4474363 | FLNC | c.1515_1520dup (p.Gly507_Glu508insSerGly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128840124G>A | CA4474365 | FLNC | c.1513G>A (p.Gly505Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840124G>C | CA369225785 | FLNC | c.1513G>C (p.Gly505Arg) | gnomAD v4 |
7 | g.128840124G= | CA1742545935 | FLNC | c.1513G= (p.Gly505=) | |
7 | g.128840124G>T | CA369225787 | FLNC | c.1513G>T (p.Gly505Cys) | |
7 | g.128840125G>A | CA4474366 | FLNC | c.1514G>A (p.Gly505Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128840125G>C | CA166216165 | FLNC | c.1514G>C (p.Gly505Ala) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128840125G= | CA1742545936 | FLNC | c.1514G= (p.Gly505=) | |
7 | g.128840125G>T | CA369225789 | FLNC | c.1514G>T (p.Gly505Val) | |
7 | g.128840126C>A | CA457582773 | FLNC | c.1515C>A (p.Gly505=) | |
7 | g.128840126C= | CA1742545937 | FLNC | c.1515C= (p.Gly505=) | |
7 | g.128840126C>G | CA457582775 | FLNC | c.1515C>G (p.Gly505=) | |
7 | g.128840126C>T | CA457582777 | FLNC | c.1515C>T (p.Gly505=) | dbSNP |
7 | g.128840126_128840133delinsCAGCGGGG | CA1742545938 | FLNC | c.1515_1522delinsCAGCGGGG (p.Gly505=) | |
7 | g.128840127A>C | CA369225791 | FLNC | c.1516A>C (p.Ser506Arg) | |
7 | g.128840127A>G | CA369225793 | FLNC | c.1516A>G (p.Ser506Gly) | |
7 | g.128840127A>T | CA369225794 | FLNC | c.1516A>T (p.Ser506Cys) | |
7 | g.128840130_128840136del | CA658657716 | FLNC | c.1519_1525del (p.Gly507SerfsTer15) | ClinVar dbSNP |
7 | g.128840128G>A | CA369225796 | FLNC | c.1517G>A (p.Ser506Asn) | ClinVar dbSNP gnomAD v4 |
7 | g.128840128G>C | CA369225798 | FLNC | c.1517G>C (p.Ser506Thr) | |
7 | g.128840128G= | CA1742545939 | FLNC | c.1517G= (p.Ser506=) | |
7 | g.128840128G>T | CA369225799 | FLNC | c.1517G>T (p.Ser506Ile) | gnomAD v4 |
7 | g.128840129C>A | CA369225803 | FLNC | c.1518C>A (p.Ser506Arg) | |
7 | g.128840129C= | CA1742545940 | FLNC | c.1518C= (p.Ser506=) | |
7 | g.128840129C>G | CA369225801 | FLNC | c.1518C>G (p.Ser506Arg) | |
7 | g.128840129C>T | CA4474367 | FLNC | c.1518C>T (p.Ser506=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840130G>A | CA4474368 | FLNC | c.1519G>A (p.Gly507Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128840130G>C | CA369225804 | FLNC | c.1519G>C (p.Gly507Arg) | |
7 | g.128840130G= | CA1742545941 | FLNC | c.1519G= (p.Gly507=) | |
7 | g.128840130G>T | CA369225805 | FLNC | c.1519G>T (p.Gly507Trp) | |
7 | g.128840131G>A | CA369225806 | FLNC | c.1520G>A (p.Gly507Glu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128840131G>C | CA369225808 | FLNC | c.1520G>C (p.Gly507Ala) | |
7 | g.128840131G= | CA1742545942 | FLNC | c.1520G= (p.Gly507=) | |
7 | g.128840131G>T | CA369225810 | FLNC | c.1520G>T (p.Gly507Val) | |
7 | g.128840132G>A | CA457582796 | FLNC | c.1521G>A (p.Gly507=) | dbSNP |
7 | g.128840132G>C | CA457582798 | FLNC | c.1521G>C (p.Gly507=) | |
7 | g.128840132G>T | CA457582800 | FLNC | c.1521G>T (p.Gly507=) | |
7 | g.128840133G>A | CA369225813 | FLNC | c.1522G>A (p.Glu508Lys) | |
7 | g.128840133G>C | CA369225815 | FLNC | c.1522G>C (p.Glu508Gln) | COSMIC |
7 | g.128840133G>T | CA369225817 | FLNC | c.1522G>T (p.Glu508Ter) | |
7 | g.128840134A>C | CA369225819 | FLNC | c.1523A>C (p.Glu508Ala) | ClinVar |
7 | g.128840134A>G | CA369225821 | FLNC | c.1523A>G (p.Glu508Gly) | |
7 | g.128840134A>T | CA369225823 | FLNC | c.1523A>T (p.Glu508Val) | |
7 | g.128840135G>A | CA457582818 | FLNC | c.1524G>A (p.Glu508=) | |
7 | g.128840135G>C | CA369225824 | FLNC | c.1524G>C (p.Glu508Asp) |