Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128847712T>A | CA369201100 | FLNC | c.4304T>A (p.Val1435Glu) | |
7 | g.128847712T>C | CA369201102 | FLNC | c.4304T>C (p.Val1435Ala) | |
7 | g.128847712T>G | CA369201098 | FLNC | c.4304T>G (p.Val1435Gly) | |
7 | g.128847713G>A | CA457848474 | FLNC | c.4305G>A (p.Val1435=) | |
7 | g.128847713G>C | CA457848475 | FLNC | c.4305G>C (p.Val1435=) | |
7 | g.128847713G>T | CA457848476 | FLNC | c.4305G>T (p.Val1435=) | |
7 | g.128847714C>A | CA369201107 | FLNC | c.4306C>A (p.Pro1436Thr) | |
7 | g.128847714C= | CA1742589232 | FLNC | c.4306C= (p.Pro1436=) | |
7 | g.128847714C>G | CA166182920 | FLNC | c.4306C>G (p.Pro1436Ala) | dbSNP |
7 | g.128847714C>T | CA369201105 | FLNC | c.4306C>T (p.Pro1436Ser) | |
7 | g.128847715C>A | CA369201110 | FLNC | c.4307C>A (p.Pro1436Gln) | |
7 | g.128847715C>G | CA369201112 | FLNC | c.4307C>G (p.Pro1436Arg) | |
7 | g.128847715C>T | CA369201113 | FLNC | c.4307C>T (p.Pro1436Leu) | |
7 | g.128847716A>C | CA457848477 | FLNC | c.4308A>C (p.Pro1436=) | |
7 | g.128847716A>G | CA457848478 | FLNC | c.4308A>G (p.Pro1436=) | |
7 | g.128847716A>T | CA457848479 | FLNC | c.4308A>T (p.Pro1436=) | |
7 | g.128847717G>A | CA369201116 | FLNC | c.4309G>A (p.Val1437Met) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128847717G>C | CA369201118 | FLNC | c.4309G>C (p.Val1437Leu) | gnomAD v4 |
7 | g.128847717G= | CA1742589235 | FLNC | c.4309G= (p.Val1437=) | |
7 | g.128847717G>T | CA369201120 | FLNC | c.4309G>T (p.Val1437Leu) | ClinVar dbSNP |
7 | g.128847718T>A | CA369201121 | FLNC | c.4310T>A (p.Val1437Glu) | |
7 | g.128847718T>C | CA166182932 | FLNC | c.4310T>C (p.Val1437Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128847718T>G | CA369201124 | FLNC | c.4310T>G (p.Val1437Gly) | |
7 | g.128847718T= | CA1742589237 | FLNC | c.4310T= (p.Val1437=) | |
7 | g.128847719G>A | CA457848480 | FLNC | c.4311G>A (p.Val1437=) | gnomAD v4 |
7 | g.128847719G>C | CA457848481 | FLNC | c.4311G>C (p.Val1437=) | |
7 | g.128847719G>T | CA457848482 | FLNC | c.4311G>T (p.Val1437=) | |
7 | g.128847720A>C | CA369201130 | FLNC | c.4312A>C (p.Lys1438Gln) | |
7 | g.128847720A>G | CA369201128 | FLNC | c.4312A>G (p.Lys1438Glu) | gnomAD v4 |
7 | g.128847720A>T | CA369201126 | FLNC | c.4312A>T (p.Lys1438Ter) | |
7 | g.128847721A>C | CA369201132 | FLNC | c.4313A>C (p.Lys1438Thr) | |
7 | g.128847721A>G | CA369201135 | FLNC | c.4313A>G (p.Lys1438Arg) | |
7 | g.128847721A>T | CA369201137 | FLNC | c.4313A>T (p.Lys1438Met) | |
7 | g.128847722G>A | CA457848483 | FLNC | c.4314G>A (p.Lys1438=) | COSMIC |
7 | g.128847722G>C | CA369201139 | FLNC | c.4314G>C (p.Lys1438Asn) | |
7 | g.128847722G>T | CA369201141 | FLNC | c.4314G>T (p.Lys1438Asn) | |
7 | g.128847723G>A | CA369201143 | FLNC | c.4315G>A (p.Asp1439Asn) | ClinVar dbSNP gnomAD v4 |
7 | g.128847723G>C | CA369201145 | FLNC | c.4315G>C (p.Asp1439His) | gnomAD v4 |
7 | g.128847723G= | CA1742589241 | FLNC | c.4315G= (p.Asp1439=) | |
7 | g.128847723G>T | CA369201147 | FLNC | c.4315G>T (p.Asp1439Tyr) | |
7 | g.128847724A>C | CA369201148 | FLNC | c.4316A>C (p.Asp1439Ala) | |
7 | g.128847724A>G | CA369201150 | FLNC | c.4316A>G (p.Asp1439Gly) | |
7 | g.128847724A>T | CA369201152 | FLNC | c.4316A>T (p.Asp1439Val) | |
7 | g.128847725T>A | CA369201154 | FLNC | c.4317T>A (p.Asp1439Glu) | dbSNP |
7 | g.128847725T>C | CA457848484 | FLNC | c.4317T>C (p.Asp1439=) | gnomAD v4 |
7 | g.128847725T>G | CA369201156 | FLNC | c.4317T>G (p.Asp1439Glu) | |
7 | g.128847725T= | CA1742589243 | FLNC | c.4317T= (p.Asp1439=) | |
7 | g.128847726G>A | CA369201161 | FLNC | c.4318G>A (p.Val1440Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128847726G>C | CA369201163 | FLNC | c.4318G>C (p.Val1440Leu) | |
7 | g.128847726G= | CA1742589246 | FLNC | c.4318G= (p.Val1440=) |