Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.119670126A= | CA1940191235 | BAG3 | c.456A= (p.Gly152=) c.282A= (p.Gly94=) | |
10 | g.119670126A>C | CA471634588 | BAG3 | c.456A>C (p.Gly152=) c.282A>C (p.Gly94=) | |
10 | g.119670126A>G | CA214220098 | BAG3 | c.456A>G (p.Gly152=) c.282A>G (p.Gly94=) | ClinVar dbSNP gnomAD v4 |
10 | g.119670126A>T | CA471634589 | BAG3 | c.456A>T (p.Gly152=) c.282A>T (p.Gly94=) | |
10 | g.119670127C>A | CA378295133 | BAG3 | c.457C>A (p.Gln153Lys) c.283C>A (p.Gln95Lys) | |
10 | g.119670127C= | CA1940191237 | BAG3 | c.457C= (p.Gln153=) c.283C= (p.Gln95=) | |
10 | g.119670127C>G | CA378295134 | BAG3 | c.457C>G (p.Gln153Glu) c.283C>G (p.Gln95Glu) | |
10 | g.119670127C>T | CA378295135 | BAG3 | c.457C>T (p.Gln153Ter) c.283C>T (p.Gln95Ter) | ClinVar dbSNP gnomAD v2 |
10 | g.119670128A>C | CA378295136 | BAG3 | c.458A>C (p.Gln153Pro) c.284A>C (p.Gln95Pro) | |
10 | g.119670128A>G | CA378295137 | BAG3 | c.458A>G (p.Gln153Arg) c.284A>G (p.Gln95Arg) | ClinVar |
10 | g.119670128A>T | CA378295138 | BAG3 | c.458A>T (p.Gln153Leu) c.284A>T (p.Gln95Leu) | |
10 | g.119670129G>A | CA471634590 | BAG3 | c.459G>A (p.Gln153=) c.285G>A (p.Gln95=) | |
10 | g.119670129G>C | CA5716321 | BAG3 | c.459G>C (p.Gln153His) c.285G>C (p.Gln95His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.119670129G= | CA1940191243 | BAG3 | c.459G= (p.Gln153=) c.285G= (p.Gln95=) | |
10 | g.119670129G>T | CA378295139 | BAG3 | c.459G>T (p.Gln153His) c.285G>T (p.Gln95His) | |
10 | g.119670131_119670142del | CA2611159847 | BAG3 | c.461_472del (p.Val154_Ala157del) c.287_298del (p.Val96_Ala99del) | gnomAD v4 |
10 | g.119670130G>A | CA5716322 | BAG3 | c.460G>A (p.Val154Met) c.286G>A (p.Val96Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670130G>C | CA16605989 | BAG3 | c.460G>C (p.Val154Leu) c.286G>C (p.Val96Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670130G= | CA1940191247 | BAG3 | c.460G= (p.Val154=) c.286G= (p.Val96=) | |
10 | g.119670130G>T | CA378295140 | BAG3 | c.460G>T (p.Val154Leu) c.286G>T (p.Val96Leu) | |
10 | g.119670131T>A | CA378295141 | BAG3 | c.461T>A (p.Val154Glu) c.287T>A (p.Val96Glu) | gnomAD v4 |
10 | g.119670131T>C | CA378295142 | BAG3 | c.461T>C (p.Val154Ala) c.287T>C (p.Val96Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
10 | g.119670131T>G | CA378295143 | BAG3 | c.461T>G (p.Val154Gly) c.287T>G (p.Val96Gly) | gnomAD v4 |
10 | g.119670131T= | CA1940191250 | BAG3 | c.461T= (p.Val154=) c.287T= (p.Val96=) | |
10 | g.119670132G>A | CA471634593 | BAG3 | c.462G>A (p.Val154=) c.288G>A (p.Val96=) | |
10 | g.119670132G>C | CA471634591 | BAG3 | c.462G>C (p.Val154=) c.288G>C (p.Val96=) | |
10 | g.119670132G>T | CA471634592 | BAG3 | c.462G>T (p.Val154=) c.288G>T (p.Val96=) | |
10 | g.119670132_119670134dup | CA660663473 | BAG3 | c.462_464dup (p.Ala155_Ala156insAla) c.288_290dup (p.Ala97_Ala98insAla) | ClinVar dbSNP gnomAD v4 |
10 | g.119670133G>A | CA135022 | BAG3 | c.463G>A (p.Ala155Thr) c.289G>A (p.Ala97Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670133G>C | CA378295144 | BAG3 | c.463G>C (p.Ala155Pro) c.289G>C (p.Ala97Pro) | |
10 | g.119670133G= | CA1940191258 | BAG3 | c.463G= (p.Ala155=) c.289G= (p.Ala97=) | |
10 | g.119670133G>T | CA378295145 | BAG3 | c.463G>T (p.Ala155Ser) c.289G>T (p.Ala97Ser) | |
10 | g.119670135_119670137dup | CA2697558794 | BAG3 | c.465_467dup (p.Ala156_Ala157insAla) c.291_293dup (p.Ala98_Ala99insAla) | ClinVar |
10 | g.119670134C>A | CA378295146 | BAG3 | c.464C>A (p.Ala155Glu) c.290C>A (p.Ala97Glu) | gnomAD v4 |
10 | g.119670134C= | CA1940191264 | BAG3 | c.464C= (p.Ala155=) c.290C= (p.Ala97=) | |
10 | g.119670134C>G | CA378295147 | BAG3 | c.464C>G (p.Ala155Gly) c.290C>G (p.Ala97Gly) | |
10 | g.119670134C>T | CA378295148 | BAG3 | c.464C>T (p.Ala155Val) c.290C>T (p.Ala97Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670135A= | CA1940191267 | BAG3 | c.465A= (p.Ala155=) c.291A= (p.Ala97=) | |
10 | g.119670135A>C | CA471634594 | BAG3 | c.465A>C (p.Ala155=) c.291A>C (p.Ala97=) | |
10 | g.119670135A>G | CA5716323 | BAG3 | c.465A>G (p.Ala155=) c.291A>G (p.Ala97=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670135A>T | CA471634595 | BAG3 | c.465A>T (p.Ala155=) c.291A>T (p.Ala97=) | |
10 | g.119670136G>A | CA378295149 | BAG3 | c.466G>A (p.Ala156Thr) c.292G>A (p.Ala98Thr) | ClinVar |
10 | g.119670136G>C | CA378295151 | BAG3 | c.466G>C (p.Ala156Pro) c.292G>C (p.Ala98Pro) | |
10 | g.119670136G>T | CA378295150 | BAG3 | c.466G>T (p.Ala156Ser) c.292G>T (p.Ala98Ser) | |
10 | g.119670136_119670137insGCG | CA1139661704 | BAG3 | c.466_467insGCG (p.Ala155_Ala156insGly) c.292_293insGCG (p.Ala97_Ala98insGly) | |
10 | g.119670144_119670146dup | CA282470 | BAG3 | c.474_476dup (p.Ala159_Ala160insAla) c.300_302dup (p.Ala101_Ala102insAla) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.119670144_119670146del | CA912966568 | BAG3 | c.474_476del (p.Ala159del) c.300_302del (p.Ala101del) | ClinVar dbSNP gnomAD v4 |
10 | g.119670137C>A | CA378295152 | BAG3 | c.467C>A (p.Ala156Glu) c.293C>A (p.Ala98Glu) | ClinVar dbSNP gnomAD v4 |
10 | g.119670137C= | CA1940191276 | BAG3 | c.467C= (p.Ala156=) c.293C= (p.Ala98=) | |
10 | g.119670137C>G | CA184149 | BAG3 | c.467C>G (p.Ala156Gly) c.293C>G (p.Ala98Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |