Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.119672256_119677283del | CA1139532250 | BAG3 | c.509_*1del | |
10 | g.119674392_119683124del | CA2580082473 | ClinVar | ||
10 | g.119675031_119678711del | CA2580082474 | ClinVar | ||
10 | g.119676621dup | CA2740093565 | BAG3 | c.1067dup (p.Pro357ThrfsTer4) c.890dup (p.Pro298ThrfsTer4) c.1064dup (p.Pro356ThrfsTer4) | ClinVar |
10 | g.119676621del | CA273654 | BAG3 | c.1067del (p.Pro356HisfsTer7) c.890del (p.Pro297HisfsTer7) c.1064del (p.Pro355HisfsTer7) | ClinVar dbSNP |
10 | g.119676621C>A | CA378296572 | BAG3 | c.1067C>A (p.Pro356Gln) c.890C>A (p.Pro297Gln) c.1064C>A (p.Pro355Gln) | |
10 | g.119676621C>G | CA378296573 | BAG3 | c.1067C>G (p.Pro356Arg) c.890C>G (p.Pro297Arg) c.1064C>G (p.Pro355Arg) | |
10 | g.119676621C>T | CA378296574 | BAG3 | c.1067C>T (p.Pro356Leu) c.890C>T (p.Pro297Leu) c.1064C>T (p.Pro355Leu) | |
10 | g.119676622A>C | CA471634897 | BAG3 | c.1068A>C (p.Pro356=) c.891A>C (p.Pro297=) c.1065A>C (p.Pro355=) | |
10 | g.119676622A>G | CA471634898 | BAG3 | c.1068A>G (p.Pro356=) c.891A>G (p.Pro297=) c.1065A>G (p.Pro355=) | ClinVar dbSNP |
10 | g.119676622A>T | CA471634899 | BAG3 | c.1068A>T (p.Pro356=) c.891A>T (p.Pro297=) c.1065A>T (p.Pro355=) | |
10 | g.119676623C>A | CA378296575 | BAG3 | c.1069C>A (p.Pro357Thr) c.892C>A (p.Pro298Thr) c.1066C>A (p.Pro356Thr) | |
10 | g.119676623C>G | CA378296576 | BAG3 | c.1069C>G (p.Pro357Ala) c.892C>G (p.Pro298Ala) c.1066C>G (p.Pro356Ala) | |
10 | g.119676623C>T | CA378296577 | BAG3 | c.1069C>T (p.Pro357Ser) c.892C>T (p.Pro298Ser) c.1066C>T (p.Pro356Ser) | |
10 | g.119676624C>A | CA378296578 | BAG3 | c.1070C>A (p.Pro357His) c.893C>A (p.Pro298His) c.1067C>A (p.Pro356His) | |
10 | g.119676624C= | CA1940196602 | BAG3 | c.1070C= (p.Pro357=) c.893C= (p.Pro298=) c.1067C= (p.Pro356=) | |
10 | g.119676624C>G | CA378296579 | BAG3 | c.1070C>G (p.Pro357Arg) c.893C>G (p.Pro298Arg) c.1067C>G (p.Pro356Arg) | |
10 | g.119676624C>T | CA5716479 | BAG3 | c.1070C>T (p.Pro357Leu) c.893C>T (p.Pro298Leu) c.1067C>T (p.Pro356Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119676625T>A | CA471634904 | BAG3 | c.1071T>A (p.Pro357=) c.894T>A (p.Pro298=) c.1068T>A (p.Pro356=) | |
10 | g.119676625T>C | CA471634906 | BAG3 | c.1071T>C (p.Pro357=) c.894T>C (p.Pro298=) c.1068T>C (p.Pro356=) | |
10 | g.119676625T>G | CA471634907 | BAG3 | c.1071T>G (p.Pro357=) c.894T>G (p.Pro298=) c.1068T>G (p.Pro356=) | |
10 | g.119676626C>A | CA378296580 | BAG3 | c.1072C>A (p.Pro358Thr) c.895C>A (p.Pro299Thr) c.1069C>A (p.Pro357Thr) | |
10 | g.119676626C= | CA1940196603 | BAG3 | c.1072C= (p.Pro358=) c.895C= (p.Pro299=) c.1069C= (p.Pro357=) | |
10 | g.119676626C>G | CA378296581 | BAG3 | c.1072C>G (p.Pro358Ala) c.895C>G (p.Pro299Ala) c.1069C>G (p.Pro357Ala) | |
10 | g.119676626C>T | CA214224857 | BAG3 | c.1072C>T (p.Pro358Ser) c.895C>T (p.Pro299Ser) c.1069C>T (p.Pro357Ser) | dbSNP gnomAD v4 COSMIC |
10 | g.119676627C>A | CA378296584 | BAG3 | c.1073C>A (p.Pro358His) c.896C>A (p.Pro299His) c.1070C>A (p.Pro357His) | |
10 | g.119676627C= | CA1940196604 | BAG3 | c.1073C= (p.Pro358=) c.896C= (p.Pro299=) c.1070C= (p.Pro357=) | |
10 | g.119676627C>G | CA378296582 | BAG3 | c.1073C>G (p.Pro358Arg) c.896C>G (p.Pro299Arg) c.1070C>G (p.Pro357Arg) | |
10 | g.119676627C>T | CA378296583 | BAG3 | c.1073C>T (p.Pro358Leu) c.896C>T (p.Pro299Leu) c.1070C>T (p.Pro357Leu) | dbSNP |
10 | g.119676628C>A | CA471634910 | BAG3 | c.1074C>A (p.Pro358=) c.897C>A (p.Pro299=) c.1071C>A (p.Pro357=) | |
10 | g.119676628C= | CA1940196605 | BAG3 | c.1074C= (p.Pro358=) c.897C= (p.Pro299=) c.1071C= (p.Pro357=) | |
10 | g.119676628C>G | CA471634911 | BAG3 | c.1074C>G (p.Pro358=) c.897C>G (p.Pro299=) c.1071C>G (p.Pro357=) | ClinVar gnomAD v4 |
10 | g.119676628C>T | CA214224861 | BAG3 | c.1074C>T (p.Pro358=) c.897C>T (p.Pro299=) c.1071C>T (p.Pro357=) | dbSNP |
10 | g.119676629T>A | CA378296585 | BAG3 | c.1075T>A (p.Ser359Thr) c.898T>A (p.Ser300Thr) c.1072T>A (p.Ser358Thr) | |
10 | g.119676629T>C | CA5716480 | BAG3 | c.1075T>C (p.Ser359Pro) c.898T>C (p.Ser300Pro) c.1072T>C (p.Ser358Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.119676629T>G | CA378296586 | BAG3 | c.1075T>G (p.Ser359Ala) c.898T>G (p.Ser300Ala) c.1072T>G (p.Ser358Ala) | |
10 | g.119676629T= | CA1940196606 | BAG3 | c.1075T= (p.Ser359=) c.898T= (p.Ser300=) c.1072T= (p.Ser358=) | |
10 | g.119676630C>A | CA378296587 | BAG3 | c.1076C>A (p.Ser359Tyr) c.899C>A (p.Ser300Tyr) c.1073C>A (p.Ser358Tyr) | |
10 | g.119676630C>G | CA378296588 | BAG3 | c.1076C>G (p.Ser359Cys) c.899C>G (p.Ser300Cys) c.1073C>G (p.Ser358Cys) | |
10 | g.119676630C>T | CA378296589 | BAG3 | c.1076C>T (p.Ser359Phe) c.899C>T (p.Ser300Phe) c.1073C>T (p.Ser358Phe) | gnomAD v4 |
10 | g.119676631T>A | CA471634912 | BAG3 | c.1077T>A (p.Ser359=) c.900T>A (p.Ser300=) c.1074T>A (p.Ser358=) | |
10 | g.119676631T>C | CA471634916 | BAG3 | c.1077T>C (p.Ser359=) c.900T>C (p.Ser300=) c.1074T>C (p.Ser358=) | |
10 | g.119676631T>G | CA471634914 | BAG3 | c.1077T>G (p.Ser359=) c.900T>G (p.Ser300=) c.1074T>G (p.Ser358=) | |
10 | g.119676632G>A | CA378296590 | BAG3 | c.1078G>A (p.Glu360Lys) c.901G>A (p.Glu301Lys) c.1075G>A (p.Glu359Lys) | |
10 | g.119676632G>C | CA378296591 | BAG3 | c.1078G>C (p.Glu360Gln) c.901G>C (p.Glu301Gln) c.1075G>C (p.Glu359Gln) | ClinVar dbSNP |
10 | g.119676632G>T | CA378296592 | BAG3 | c.1078G>T (p.Glu360Ter) c.901G>T (p.Glu301Ter) c.1075G>T (p.Glu359Ter) | COSMIC |
10 | g.119676633A>C | CA378296593 | BAG3 | c.1079A>C (p.Glu360Ala) c.902A>C (p.Glu301Ala) c.1076A>C (p.Glu359Ala) | |
10 | g.119676633A>G | CA378296594 | BAG3 | c.1079A>G (p.Glu360Gly) c.902A>G (p.Glu301Gly) c.1076A>G (p.Glu359Gly) | |
10 | g.119676633A>T | CA378296595 | BAG3 | c.1079A>T (p.Glu360Val) c.902A>T (p.Glu301Val) c.1076A>T (p.Glu359Val) | |
10 | g.119676634G>A | CA471634919 | BAG3 | c.1080G>A (p.Glu360=) c.903G>A (p.Glu301=) c.1077G>A (p.Glu359=) |