Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128838415A>C | CA369224307 | FLNC | c.1196A>C (p.Asp399Ala) | |
7 | g.128838415A>G | CA369224308 | FLNC | c.1196A>G (p.Asp399Gly) | |
7 | g.128838415A>T | CA369224309 | FLNC | c.1196A>T (p.Asp399Val) | gnomAD v4 |
7 | g.128838418_128838423del | CA2695199636 | FLNC | c.1199_1204del (p.Ile400_Tyr401del) | ClinVar |
7 | g.128838416del | CA2684819871 | FLNC | c.1197del (p.Asp399GlufsTer15) | gnomAD v4 |
7 | g.128838416C>A | CA369224310 | FLNC | c.1197C>A (p.Asp399Glu) | |
7 | g.128838416C= | CA1742545097 | FLNC | c.1197C= (p.Asp399=) | |
7 | g.128838416C>G | CA369224311 | FLNC | c.1197C>G (p.Asp399Glu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128838416C>T | CA4474254 | FLNC | c.1197C>T (p.Asp399=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128838417A>C | CA369224312 | FLNC | c.1198A>C (p.Ile400Leu) | |
7 | g.128838417A>G | CA369224314 | FLNC | c.1198A>G (p.Ile400Val) | |
7 | g.128838417A>T | CA369224313 | FLNC | c.1198A>T (p.Ile400Phe) | |
7 | g.128838418T>A | CA369224315 | FLNC | c.1199T>A (p.Ile400Asn) | |
7 | g.128838418T>C | CA369224317 | FLNC | c.1199T>C (p.Ile400Thr) | ClinVar dbSNP |
7 | g.128838418T>G | CA369224316 | FLNC | c.1199T>G (p.Ile400Ser) | |
7 | g.128838418T= | CA1742545098 | FLNC | c.1199T= (p.Ile400=) | |
7 | g.128838419C>A | CA457846445 | FLNC | c.1200C>A (p.Ile400=) | |
7 | g.128838419C= | CA1742545099 | FLNC | c.1200C= (p.Ile400=) | |
7 | g.128838419C>G | CA369224318 | FLNC | c.1200C>G (p.Ile400Met) | |
7 | g.128838419C>T | CA4474255 | FLNC | c.1200C>T (p.Ile400=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128838420T>A | CA369224319 | FLNC | c.1201T>A (p.Tyr401Asn) | |
7 | g.128838420T>C | CA369224320 | FLNC | c.1201T>C (p.Tyr401His) | |
7 | g.128838420T>G | CA369224321 | FLNC | c.1201T>G (p.Tyr401Asp) | |
7 | g.128838421A>C | CA369224322 | FLNC | c.1202A>C (p.Tyr401Ser) | gnomAD v4 |
7 | g.128838421A>G | CA369224323 | FLNC | c.1202A>G (p.Tyr401Cys) | |
7 | g.128838421A>T | CA369224324 | FLNC | c.1202A>T (p.Tyr401Phe) | |
7 | g.128838422C>A | CA369224325 | FLNC | c.1203C>A (p.Tyr401Ter) | |
7 | g.128838422C>G | CA369224326 | FLNC | c.1203C>G (p.Tyr401Ter) | |
7 | g.128838422C>T | CA457846449 | FLNC | c.1203C>T (p.Tyr401=) | |
7 | g.128838423A>C | CA369224327 | FLNC | c.1204A>C (p.Thr402Pro) | |
7 | g.128838423A>G | CA369224328 | FLNC | c.1204A>G (p.Thr402Ala) | |
7 | g.128838423A>T | CA369224329 | FLNC | c.1204A>T (p.Thr402Ser) | |
7 | g.128838424del | CA2499218718 | FLNC | c.1205del (p.Thr402MetfsTer12) | ClinVar dbSNP |
7 | g.128838424C>A | CA369224331 | FLNC | c.1205C>A (p.Thr402Asn) | |
7 | g.128838424C= | CA1742545100 | FLNC | c.1205C= (p.Thr402=) | |
7 | g.128838424C>G | CA369224330 | FLNC | c.1205C>G (p.Thr402Ser) | |
7 | g.128838424C>T | CA4474256 | FLNC | c.1205C>T (p.Thr402Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128838425T>A | CA457846450 | FLNC | c.1206T>A (p.Thr402=) | ClinVar dbSNP gnomAD v4 |
7 | g.128838425T>C | CA457846451 | FLNC | c.1206T>C (p.Thr402=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128838425T>G | CA4474257 | FLNC | c.1206T>G (p.Thr402=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128838425T= | CA1742545101 | FLNC | c.1206T= (p.Thr402=) | |
7 | g.128838425_128838426dup | CA2740097539 | FLNC | c.1206_1207dup (p.Ala403ValfsTer12) | ClinVar |
7 | g.128838426G>A | CA369224332 | FLNC | c.1207G>A (p.Ala403Thr) | |
7 | g.128838426G>C | CA369224333 | FLNC | c.1207G>C (p.Ala403Pro) | |
7 | g.128838426G>T | CA369224334 | FLNC | c.1207G>T (p.Ala403Ser) | |
7 | g.128838427C>A | CA369224335 | FLNC | c.1208C>A (p.Ala403Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128838427C= | CA1742545102 | FLNC | c.1208C= (p.Ala403=) | |
7 | g.128838427C>G | CA369224336 | FLNC | c.1208C>G (p.Ala403Gly) | |
7 | g.128838427C>T | CA4474258 | FLNC | c.1208C>T (p.Ala403Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128838428G>A | CA4474259 | FLNC | c.1209G>A (p.Ala403=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |