| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.119672256_119677283del | CA1139532250 | BAG3 | c.509_*1del | |
| 10 | g.119672304_119672328delinsCCAGCCTGCCTTCCTCCGGCAGGAG | CA1940193130 | BAG3 | c.557_581delinsCCAGCCTGCCTTCCTCCGGCAGGAG (p.Ala186=) c.383_407delinsCCAGCCTGCCTTCCTCCGGCAGGAG (p.Ala128=) | |
| 10 | g.119672312_119672335del | CA1940193132 | BAG3 | c.565_588del (p.Pro189_Leu196del) c.391_414del (p.Pro131_Leu138del) | ClinVar dbSNP |
| 10 | g.119672312_119672327del | CA2611160108 | BAG3 | c.565_580del (p.Pro189AlafsTer17) c.391_406del (p.Pro131AlafsTer17) | gnomAD v4 |
| 10 | g.119672314_119672324delinsTTCCTCCGGCA | CA1940193140 | BAG3 | c.567_577delinsTTCCTCCGGCA (p.Pro189=) c.393_403delinsTTCCTCCGGCA (p.Pro131=) | |
| 10 | g.119672315_119672324del | CA1139661705 | BAG3 | c.568_577del (p.Ser190GlyfsTer18) c.394_403del (p.Ser132GlyfsTer18) | ClinVar dbSNP |
| 10 | g.119672319C>A | CA378295362 | BAG3 | c.572C>A (p.Ser191Tyr) c.398C>A (p.Ser133Tyr) | |
| 10 | g.119672319C>G | CA378295363 | BAG3 | c.572C>G (p.Ser191Cys) c.398C>G (p.Ser133Cys) | |
| 10 | g.119672319C>T | CA378295364 | BAG3 | c.572C>T (p.Ser191Phe) c.398C>T (p.Ser133Phe) | |
| 10 | g.119672320C>A | CA471739195 | BAG3 | c.573C>A (p.Ser191=) c.399C>A (p.Ser133=) | |
| 10 | g.119672320C= | CA1940193157 | BAG3 | c.573C= (p.Ser191=) c.399C= (p.Ser133=) | |
| 10 | g.119672320C>G | CA471739196 | BAG3 | c.573C>G (p.Ser191=) c.399C>G (p.Ser133=) | |
| 10 | g.119672320C>T | CA5716367 | BAG3 | c.573C>T (p.Ser191=) c.399C>T (p.Ser133=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.119672320_119672321insTCT | CA1940193164 | BAG3 | c.573_574insTCT (p.Ser191_Gly192insSer) c.399_400insTCT (p.Ser133_Gly134insSer) | dbSNP |
| 10 | g.119672321G>A | CA5716368 | BAG3 | c.574G>A (p.Gly192Ser) c.400G>A (p.Gly134Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672321G>C | CA378295365 | BAG3 | c.574G>C (p.Gly192Arg) c.400G>C (p.Gly134Arg) | |
| 10 | g.119672321G= | CA1940193165 | BAG3 | c.574G= (p.Gly192=) c.400G= (p.Gly134=) | |
| 10 | g.119672321G>T | CA5716369 | BAG3 | c.574G>T (p.Gly192Cys) c.400G>T (p.Gly134Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672322G>A | CA378295366 | BAG3 | c.575G>A (p.Gly192Asp) c.401G>A (p.Gly134Asp) | |
| 10 | g.119672322G>C | CA378295367 | BAG3 | c.575G>C (p.Gly192Ala) c.401G>C (p.Gly134Ala) | |
| 10 | g.119672322G>T | CA378295368 | BAG3 | c.575G>T (p.Gly192Val) c.401G>T (p.Gly134Val) | |
| 10 | g.119672323C>A | CA471739197 | BAG3 | c.576C>A (p.Gly192=) c.402C>A (p.Gly134=) | |
| 10 | g.119672323C= | CA1940193170 | BAG3 | c.576C= (p.Gly192=) c.402C= (p.Gly134=) | |
| 10 | g.119672323C>G | CA471739199 | BAG3 | c.576C>G (p.Gly192=) c.402C>G (p.Gly134=) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672323C>T | CA471739198 | BAG3 | c.576C>T (p.Gly192=) c.402C>T (p.Gly134=) | ClinVar dbSNP |
| 10 | g.119672324A>C | CA471739200 | BAG3 | c.577A>C (p.Arg193=) c.403A>C (p.Arg135=) | |
| 10 | g.119672324A>G | CA378295369 | BAG3 | c.577A>G (p.Arg193Gly) c.403A>G (p.Arg135Gly) | ClinVar |
| 10 | g.119672324A>T | CA378295370 | BAG3 | c.577A>T (p.Arg193Trp) c.403A>T (p.Arg135Trp) | |
| 10 | g.119672325G>A | CA5716370 | BAG3 | c.578G>A (p.Arg193Lys) c.404G>A (p.Arg135Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.119672325G>C | CA378295372 | BAG3 | c.578G>C (p.Arg193Thr) c.404G>C (p.Arg135Thr) | |
| 10 | g.119672325G= | CA1940193177 | BAG3 | c.578G= (p.Arg193=) c.404G= (p.Arg135=) | |
| 10 | g.119672325G>T | CA378295371 | BAG3 | c.578G>T (p.Arg193Met) c.404G>T (p.Arg135Met) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672326G>A | CA471739201 | BAG3 | c.579G>A (p.Arg193=) c.405G>A (p.Arg135=) | |
| 10 | g.119672326G>C | CA378295373 | BAG3 | c.579G>C (p.Arg193Ser) c.405G>C (p.Arg135Ser) | |
| 10 | g.119672326G>T | CA378295374 | BAG3 | c.579G>T (p.Arg193Ser) c.405G>T (p.Arg135Ser) | |
| 10 | g.119672326_119672327delinsGA | CA1940193180 | BAG3 | c.579_580delinsGA (p.Arg193=) c.405_406delinsGA (p.Arg135=) | |
| 10 | g.119672327del | CA16618934 | BAG3 | c.580del (p.Ser194AlafsTer17) c.406del (p.Ser136AlafsTer17) | ClinVar dbSNP |
| 10 | g.119672327A= | CA1940193184 | BAG3 | c.580A= (p.Ser194=) c.406A= (p.Ser136=) | |
| 10 | g.119672327A>C | CA378295375 | BAG3 | c.580A>C (p.Ser194Arg) c.406A>C (p.Ser136Arg) | |
| 10 | g.119672327A>G | CA378295376 | BAG3 | c.580A>G (p.Ser194Gly) c.406A>G (p.Ser136Gly) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.119672327A>T | CA378295377 | BAG3 | c.580A>T (p.Ser194Cys) c.406A>T (p.Ser136Cys) | |
| 10 | g.119672328G>A | CA378295380 | BAG3 | c.581G>A (p.Ser194Asn) c.407G>A (p.Ser136Asn) | |
| 10 | g.119672328G>C | CA378295378 | BAG3 | c.581G>C (p.Ser194Thr) c.407G>C (p.Ser136Thr) | |
| 10 | g.119672328G>T | CA378295379 | BAG3 | c.581G>T (p.Ser194Ile) c.407G>T (p.Ser136Ile) | |
| 10 | g.119672329C>A | CA378295381 | BAG3 | c.582C>A (p.Ser194Arg) c.408C>A (p.Ser136Arg) | |
| 10 | g.119672329C= | CA1940193187 | BAG3 | c.582C= (p.Ser194=) c.408C= (p.Ser136=) | |
| 10 | g.119672329C>G | CA214221693 | BAG3 | c.582C>G (p.Ser194Arg) c.408C>G (p.Ser136Arg) | ClinVar dbSNP |
| 10 | g.119672329C>T | CA471739202 | BAG3 | c.582C>T (p.Ser194=) c.408C>T (p.Ser136=) | |
| 10 | g.119672330A= | CA1940193189 | BAG3 | c.583A= (p.Ser195=) c.409A= (p.Ser137=) | |
| 10 | g.119672330A>C | CA378295382 | BAG3 | c.583A>C (p.Ser195Arg) c.409A>C (p.Ser137Arg) | |
| 10 | g.119672330A>G | CA5716371 | BAG3 | c.583A>G (p.Ser195Gly) c.409A>G (p.Ser137Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672330A>T | CA378295383 | BAG3 | c.583A>T (p.Ser195Cys) c.409A>T (p.Ser137Cys) | |
| 10 | g.119672331G>A | CA5716372 | BAG3 | c.584G>A (p.Ser195Asn) c.410G>A (p.Ser137Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672331G>C | CA378295385 | BAG3 | c.584G>C (p.Ser195Thr) c.410G>C (p.Ser137Thr) | |
| 10 | g.119672331G= | CA1940193192 | BAG3 | c.584G= (p.Ser195=) c.410G= (p.Ser137=) | |
| 10 | g.119672331G>T | CA378295384 | BAG3 | c.584G>T (p.Ser195Ile) c.410G>T (p.Ser137Ile) | |
| 10 | g.119672332C>A | CA378295386 | BAG3 | c.585C>A (p.Ser195Arg) c.411C>A (p.Ser137Arg) | |
| 10 | g.119672332C= | CA1940193197 | BAG3 | c.585C= (p.Ser195=) c.411C= (p.Ser137=) | |
| 10 | g.119672332C>G | CA378295387 | BAG3 | c.585C>G (p.Ser195Arg) c.411C>G (p.Ser137Arg) | |
| 10 | g.119672332C>T | CA471739203 | BAG3 | c.585C>T (p.Ser195=) c.411C>T (p.Ser137=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672333C>A | CA378295388 | BAG3 | c.586C>A (p.Leu196Met) c.412C>A (p.Leu138Met) | |
| 10 | g.119672333C= | CA1940193199 | BAG3 | c.586C= (p.Leu196=) c.412C= (p.Leu138=) | |
| 10 | g.119672333C>G | CA214221700 | BAG3 | c.586C>G (p.Leu196Val) c.412C>G (p.Leu138Val) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672333C>T | CA471739204 | BAG3 | c.586C>T (p.Leu196=) c.412C>T (p.Leu138=) | |
| 10 | g.119672334T>A | CA378295389 | BAG3 | c.587T>A (p.Leu196Gln) c.413T>A (p.Leu138Gln) | |
| 10 | g.119672334T>C | CA378295390 | BAG3 | c.587T>C (p.Leu196Pro) c.413T>C (p.Leu138Pro) | |
| 10 | g.119672334T>G | CA378295391 | BAG3 | c.587T>G (p.Leu196Arg) c.413T>G (p.Leu138Arg) | |
| 10 | g.119672335G>A | CA471739205 | BAG3 | c.588G>A (p.Leu196=) c.414G>A (p.Leu138=) | |
| 10 | g.119672335G>C | CA471739207 | BAG3 | c.588G>C (p.Leu196=) c.414G>C (p.Leu138=) | |
| 10 | g.119672335G>T | CA471739206 | BAG3 | c.588G>T (p.Leu196=) c.414G>T (p.Leu138=) | |
| 10 | g.119672336G>A | CA5716373 | BAG3 | c.589G>A (p.Gly197Ser) c.415G>A (p.Gly139Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672336G>C | CA378295392 | BAG3 | c.589G>C (p.Gly197Arg) c.415G>C (p.Gly139Arg) | |
| 10 | g.119672336G= | CA1940193202 | BAG3 | c.589G= (p.Gly197=) c.415G= (p.Gly139=) | |
| 10 | g.119672336G>T | CA378295393 | BAG3 | c.589G>T (p.Gly197Cys) c.415G>T (p.Gly139Cys) | COSMIC |
| 10 | g.119672337G>A | CA5716374 | BAG3 | c.590G>A (p.Gly197Asp) c.416G>A (p.Gly139Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672337G>C | CA378295394 | BAG3 | c.590G>C (p.Gly197Ala) c.416G>C (p.Gly139Ala) | |
| 10 | g.119672337G= | CA1940193204 | BAG3 | c.590G= (p.Gly197=) c.416G= (p.Gly139=) | |
| 10 | g.119672337G>T | CA378295395 | BAG3 | c.590G>T (p.Gly197Val) c.416G>T (p.Gly139Val) | |
| 10 | g.119672338C>A | CA471739208 | BAG3 | c.591C>A (p.Gly197=) c.417C>A (p.Gly139=) | |
| 10 | g.119672338C= | CA1940193208 | BAG3 | c.591C= (p.Gly197=) c.417C= (p.Gly139=) | |
| 10 | g.119672338C>G | CA471739209 | BAG3 | c.591C>G (p.Gly197=) c.417C>G (p.Gly139=) | |
| 10 | g.119672338C>T | CA471739210 | BAG3 | c.591C>T (p.Gly197=) c.417C>T (p.Gly139=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672339A>C | CA378295396 | BAG3 | c.592A>C (p.Ser198Arg) c.418A>C (p.Ser140Arg) | |
| 10 | g.119672339A>G | CA378295397 | BAG3 | c.592A>G (p.Ser198Gly) c.418A>G (p.Ser140Gly) | |
| 10 | g.119672339A>T | CA378295398 | BAG3 | c.592A>T (p.Ser198Cys) c.418A>T (p.Ser140Cys) | ClinVar |
| 10 | g.119672340G>A | CA378295401 | BAG3 | c.593G>A (p.Ser198Asn) c.419G>A (p.Ser140Asn) | |
| 10 | g.119672340G>C | CA378295399 | BAG3 | c.593G>C (p.Ser198Thr) c.419G>C (p.Ser140Thr) | |
| 10 | g.119672340G>T | CA378295400 | BAG3 | c.593G>T (p.Ser198Ile) c.419G>T (p.Ser140Ile) | |
| 10 | g.119672341T>A | CA378295402 | BAG3 | c.594T>A (p.Ser198Arg) c.420T>A (p.Ser140Arg) | |
| 10 | g.119672341T>C | CA471739211 | BAG3 | c.594T>C (p.Ser198=) c.420T>C (p.Ser140=) | |
| 10 | g.119672341T>G | CA378295403 | BAG3 | c.594T>G (p.Ser198Arg) c.420T>G (p.Ser140Arg) | |
| 10 | g.119672342C>A | CA378295404 | BAG3 | c.595C>A (p.His199Asn) c.421C>A (p.His141Asn) | |
| 10 | g.119672342C= | CA1940193212 | BAG3 | c.595C= (p.His199=) c.421C= (p.His141=) | |
| 10 | g.119672342C>G | CA378295405 | BAG3 | c.595C>G (p.His199Asp) c.421C>G (p.His141Asp) | |
| 10 | g.119672342C>T | CA5716375 | BAG3 | c.595C>T (p.His199Tyr) c.421C>T (p.His141Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672343A>C | CA378295406 | BAG3 | c.596A>C (p.His199Pro) c.422A>C (p.His141Pro) | |
| 10 | g.119672343A>G | CA378295407 | BAG3 | c.596A>G (p.His199Arg) c.422A>G (p.His141Arg) | |
| 10 | g.119672343A>T | CA378295408 | BAG3 | c.596A>T (p.His199Leu) c.422A>T (p.His141Leu) | |
| 10 | g.119672344C>A | CA378295409 | BAG3 | c.597C>A (p.His199Gln) c.423C>A (p.His141Gln) | |
| 10 | g.119672344C= | CA1940193216 | BAG3 | c.597C= (p.His199=) c.423C= (p.His141=) | |
| 10 | g.119672344C>G | CA378295410 | BAG3 | c.597C>G (p.His199Gln) c.423C>G (p.His141Gln) | |
| 10 | g.119672344C>T | CA5716376 | BAG3 | c.597C>T (p.His199=) c.423C>T (p.His141=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672345C>A | CA378295413 | BAG3 | c.598C>A (p.Gln200Lys) c.424C>A (p.Gln142Lys) | |
| 10 | g.119672345C>G | CA378295412 | BAG3 | c.598C>G (p.Gln200Glu) c.424C>G (p.Gln142Glu) | |
| 10 | g.119672345C>T | CA378295411 | BAG3 | c.598C>T (p.Gln200Ter) c.424C>T (p.Gln142Ter) | ClinVar dbSNP COSMIC |
| 10 | g.119672346A= | CA1940193218 | BAG3 | c.599A= (p.Gln200=) c.425A= (p.Gln142=) | |
| 10 | g.119672346A>C | CA378295414 | BAG3 | c.599A>C (p.Gln200Pro) c.425A>C (p.Gln142Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672346A>G | CA378295415 | BAG3 | c.599A>G (p.Gln200Arg) c.425A>G (p.Gln142Arg) | dbSNP gnomAD v4 |
| 10 | g.119672346A>T | CA378295416 | BAG3 | c.599A>T (p.Gln200Leu) c.425A>T (p.Gln142Leu) | |
| 10 | g.119672347G>A | CA471739744 | BAG3 | c.600G>A (p.Gln200=) c.426G>A (p.Gln142=) | |
| 10 | g.119672347G>C | CA5716377 | BAG3 | c.600G>C (p.Gln200His) c.426G>C (p.Gln142His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672347G= | CA1940193219 | BAG3 | c.600G= (p.Gln200=) c.426G= (p.Gln142=) | |
| 10 | g.119672347G>T | CA378295417 | BAG3 | c.600G>T (p.Gln200His) c.426G>T (p.Gln142His) | |
| 10 | g.119672348C>A | CA378295418 | BAG3 | c.601C>A (p.Leu201Ile) c.427C>A (p.Leu143Ile) | |
| 10 | g.119672348C>G | CA378295419 | BAG3 | c.601C>G (p.Leu201Val) c.427C>G (p.Leu143Val) | dbSNP gnomAD v4 |
| 10 | g.119672348C>T | CA378295420 | BAG3 | c.601C>T (p.Leu201Phe) c.427C>T (p.Leu143Phe) | gnomAD v4 |
| 10 | g.119672349T>A | CA378295421 | BAG3 | c.602T>A (p.Leu201His) c.428T>A (p.Leu143His) | |
| 10 | g.119672349T>C | CA214221721 | BAG3 | c.602T>C (p.Leu201Pro) c.428T>C (p.Leu143Pro) | dbSNP |
| 10 | g.119672349T>G | CA378295422 | BAG3 | c.602T>G (p.Leu201Arg) c.428T>G (p.Leu143Arg) | dbSNP |
| 10 | g.119672349T= | CA1940193223 | BAG3 | c.602T= (p.Leu201=) c.428T= (p.Leu143=) | |
| 10 | g.119672350C>A | CA471739745 | BAG3 | c.603C>A (p.Leu201=) c.429C>A (p.Leu143=) | |
| 10 | g.119672350C= | CA1940193225 | BAG3 | c.603C= (p.Leu201=) c.429C= (p.Leu143=) | |
| 10 | g.119672350C>G | CA471739746 | BAG3 | c.603C>G (p.Leu201=) c.429C>G (p.Leu143=) | dbSNP |
| 10 | g.119672350C>T | CA471739747 | BAG3 | c.603C>T (p.Leu201=) c.429C>T (p.Leu143=) | |
| 10 | g.119672351C>A | CA378295425 | BAG3 | c.604C>A (p.Pro202Thr) c.430C>A (p.Pro144Thr) | |
| 10 | g.119672351C>G | CA378295424 | BAG3 | c.604C>G (p.Pro202Ala) c.430C>G (p.Pro144Ala) | |
| 10 | g.119672351C>T | CA378295423 | BAG3 | c.604C>T (p.Pro202Ser) c.430C>T (p.Pro144Ser) | |
| 10 | g.119672352C>A | CA378295426 | BAG3 | c.605C>A (p.Pro202Gln) c.431C>A (p.Pro144Gln) | |
| 10 | g.119672352C= | CA1940193229 | BAG3 | c.605C= (p.Pro202=) c.431C= (p.Pro144=) | |
| 10 | g.119672352C>G | CA378295427 | BAG3 | c.605C>G (p.Pro202Arg) c.431C>G (p.Pro144Arg) | |
| 10 | g.119672352C>T | CA5716378 | BAG3 | c.605C>T (p.Pro202Leu) c.431C>T (p.Pro144Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672353G>A | CA5716379 | BAG3 | c.606G>A (p.Pro202=) c.432G>A (p.Pro144=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672353G>C | CA471739748 | BAG3 | c.606G>C (p.Pro202=) c.432G>C (p.Pro144=) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672353G= | CA1940193232 | BAG3 | c.606G= (p.Pro202=) c.432G= (p.Pro144=) | |
| 10 | g.119672353G>T | CA282473 | BAG3 | c.606G>T (p.Pro202=) c.432G>T (p.Pro144=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672354C>A | CA214221736 | BAG3 | c.607C>A (p.Arg203=) c.433C>A (p.Arg145=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.119672354C= | CA1940193237 | BAG3 | c.607C= (p.Arg203=) c.433C= (p.Arg145=) | |
| 10 | g.119672354C>G | CA378295428 | BAG3 | c.607C>G (p.Arg203Gly) c.433C>G (p.Arg145Gly) | gnomAD v4 |
| 10 | g.119672354C>T | CA378295429 | BAG3 | c.607C>T (p.Arg203Trp) c.433C>T (p.Arg145Trp) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 10 | g.119672354dup | CA16612935 | BAG3 | c.607dup (p.Arg203ProfsTer?) c.433dup (p.Arg145ProfsTer?) | ClinVar dbSNP |
| 10 | g.119672355G>A | CA16605610 | BAG3 | c.608G>A (p.Arg203Gln) c.434G>A (p.Arg145Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672355G>C | CA378295430 | BAG3 | c.608G>C (p.Arg203Pro) c.434G>C (p.Arg145Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672355G= | CA1940193244 | BAG3 | c.608G= (p.Arg203=) c.434G= (p.Arg145=) | |
| 10 | g.119672355G>T | CA378295431 | BAG3 | c.608G>T (p.Arg203Leu) c.434G>T (p.Arg145Leu) | gnomAD v4 |
| 10 | g.119672359del | CA2573145589 | BAG3 | c.612del (p.Tyr205ThrfsTer6) c.438del (p.Tyr147ThrfsTer6) | ClinVar dbSNP |
| 10 | g.119672356G>A | CA471739750 | BAG3 | c.609G>A (p.Arg203=) c.435G>A (p.Arg145=) | |
| 10 | g.119672356G>C | CA471739751 | BAG3 | c.609G>C (p.Arg203=) c.435G>C (p.Arg145=) | ClinVar dbSNP |
| 10 | g.119672356G= | CA1940193246 | BAG3 | c.609G= (p.Arg203=) c.435G= (p.Arg145=) | |
| 10 | g.119672356G>T | CA471739749 | BAG3 | c.609G>T (p.Arg203=) c.435G>T (p.Arg145=) | |
| 10 | g.119672357G>A | CA378295432 | BAG3 | c.610G>A (p.Gly204Arg) c.436G>A (p.Gly146Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672357G>C | CA378295433 | BAG3 | c.610G>C (p.Gly204Arg) c.436G>C (p.Gly146Arg) | |
| 10 | g.119672357G= | CA1940193249 | BAG3 | c.610G= (p.Gly204=) c.436G= (p.Gly146=) | |
| 10 | g.119672357G>T | CA378295434 | BAG3 | c.610G>T (p.Gly204Trp) c.436G>T (p.Gly146Trp) | |
| 10 | g.119672358G>A | CA378295435 | BAG3 | c.611G>A (p.Gly204Glu) c.437G>A (p.Gly146Glu) | |
| 10 | g.119672358G>C | CA378295436 | BAG3 | c.611G>C (p.Gly204Ala) c.437G>C (p.Gly146Ala) | |
| 10 | g.119672358G= | CA1940193250 | BAG3 | c.611G= (p.Gly204=) c.437G= (p.Gly146=) | |
| 10 | g.119672358G>T | CA5716380 | BAG3 | c.611G>T (p.Gly204Val) c.437G>T (p.Gly146Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672359G>A | CA471739754 | BAG3 | c.612G>A (p.Gly204=) c.438G>A (p.Gly146=) | ClinVar dbSNP |
| 10 | g.119672359G>C | CA471739753 | BAG3 | c.612G>C (p.Gly204=) c.438G>C (p.Gly146=) | |
| 10 | g.119672359G>T | CA471739752 | BAG3 | c.612G>T (p.Gly204=) c.438G>T (p.Gly146=) | |
| 10 | g.119672359_119672360delinsGT | CA1940193252 | BAG3 | c.612_613delinsGT (p.Gly204=) c.438_439delinsGT (p.Gly146=) | |
| 10 | g.119672360del | CA915948733 | BAG3 | c.613del (p.Tyr205ThrfsTer6) c.439del (p.Tyr147ThrfsTer6) | |
| 10 | g.119672360T>A | CA378295438 | BAG3 | c.613T>A (p.Tyr205Asn) c.439T>A (p.Tyr147Asn) | |
| 10 | g.119672360T>C | CA5716381 | BAG3 | c.613T>C (p.Tyr205His) c.439T>C (p.Tyr147His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672360T>G | CA378295437 | BAG3 | c.613T>G (p.Tyr205Asp) c.439T>G (p.Tyr147Asp) | dbSNP |
| 10 | g.119672360T= | CA1940193258 | BAG3 | c.613T= (p.Tyr205=) c.439T= (p.Tyr147=) | |
| 10 | g.119672361A= | CA1940193267 | BAG3 | c.614A= (p.Tyr205=) c.440A= (p.Tyr147=) | |
| 10 | g.119672361A>C | CA378295439 | BAG3 | c.614A>C (p.Tyr205Ser) c.440A>C (p.Tyr147Ser) | |
| 10 | g.119672361A>G | CA378295440 | BAG3 | c.614A>G (p.Tyr205Cys) c.440A>G (p.Tyr147Cys) | gnomAD v4 COSMIC |
| 10 | g.119672361A>T | CA5716382 | BAG3 | c.614A>T (p.Tyr205Phe) c.440A>T (p.Tyr147Phe) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 10 | g.119672362C>A | CA378295441 | BAG3 | c.615C>A (p.Tyr205Ter) c.441C>A (p.Tyr147Ter) | |
| 10 | g.119672362C= | CA1940193269 | BAG3 | c.615C= (p.Tyr205=) c.441C= (p.Tyr147=) | |
| 10 | g.119672362C>G | CA378295442 | BAG3 | c.615C>G (p.Tyr205Ter) c.441C>G (p.Tyr147Ter) | |
| 10 | g.119672362C>T | CA214221744 | BAG3 | c.615C>T (p.Tyr205=) c.441C>T (p.Tyr147=) | dbSNP |
| 10 | g.119672363A= | CA1940193279 | BAG3 | c.616A= (p.Ile206=) c.442A= (p.Ile148=) | |
| 10 | g.119672363A>C | CA5716383 | BAG3 | c.616A>C (p.Ile206Leu) c.442A>C (p.Ile148Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672363A>G | CA237049 | BAG3 | c.616A>G (p.Ile206Val) c.442A>G (p.Ile148Val) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672363A>T | CA378295443 | BAG3 | c.616A>T (p.Ile206Phe) c.442A>T (p.Ile148Phe) | gnomAD v4 |
| 10 | g.119672364T>A | CA378295444 | BAG3 | c.617T>A (p.Ile206Asn) c.443T>A (p.Ile148Asn) | |
| 10 | g.119672364T>C | CA378295445 | BAG3 | c.617T>C (p.Ile206Thr) c.443T>C (p.Ile148Thr) | |
| 10 | g.119672364T>G | CA378295446 | BAG3 | c.617T>G (p.Ile206Ser) c.443T>G (p.Ile148Ser) | |
| 10 | g.119672365C>A | CA471739755 | BAG3 | c.618C>A (p.Ile206=) c.444C>A (p.Ile148=) | |
| 10 | g.119672365C= | CA1940193285 | BAG3 | c.618C= (p.Ile206=) c.444C= (p.Ile148=) | |
| 10 | g.119672365C>G | CA378295447 | BAG3 | c.618C>G (p.Ile206Met) c.444C>G (p.Ile148Met) | ClinVar dbSNP |
| 10 | g.119672365C>T | CA471739756 | BAG3 | c.618C>T (p.Ile206=) c.444C>T (p.Ile148=) | |
| 10 | g.119672366T>A | CA378295448 | BAG3 | c.619T>A (p.Ser207Thr) c.445T>A (p.Ser149Thr) | |
| 10 | g.119672366T>C | CA378295449 | BAG3 | c.619T>C (p.Ser207Pro) c.445T>C (p.Ser149Pro) | |
| 10 | g.119672366T>G | CA378295450 | BAG3 | c.619T>G (p.Ser207Ala) c.445T>G (p.Ser149Ala) | |
| 10 | g.119672367C>A | CA378295451 | BAG3 | c.620C>A (p.Ser207Tyr) c.446C>A (p.Ser149Tyr) | dbSNP |
| 10 | g.119672367C= | CA1940193289 | BAG3 | c.620C= (p.Ser207=) c.446C= (p.Ser149=) | |
| 10 | g.119672367C>G | CA378295452 | BAG3 | c.620C>G (p.Ser207Cys) c.446C>G (p.Ser149Cys) | |
| 10 | g.119672367C>T | CA5716384 | BAG3 | c.620C>T (p.Ser207Phe) c.446C>T (p.Ser149Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672368C>A | CA471739757 | BAG3 | c.621C>A (p.Ser207=) c.447C>A (p.Ser149=) | |
| 10 | g.119672368C>G | CA471739758 | BAG3 | c.621C>G (p.Ser207=) c.447C>G (p.Ser149=) | |
| 10 | g.119672368C>T | CA471739759 | BAG3 | c.621C>T (p.Ser207=) c.447C>T (p.Ser149=) | |
| 10 | g.119672369A= | CA1940193295 | BAG3 | c.622A= (p.Ile208=) c.448A= (p.Ile150=) | |
| 10 | g.119672369A>C | CA214221754 | BAG3 | c.622A>C (p.Ile208Leu) c.448A>C (p.Ile150Leu) | ClinVar dbSNP |
| 10 | g.119672369A>G | CA378295453 | BAG3 | c.622A>G (p.Ile208Val) c.448A>G (p.Ile150Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.119672369A>T | CA378295454 | BAG3 | c.622A>T (p.Ile208Phe) c.448A>T (p.Ile150Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672370T>A | CA378295455 | BAG3 | c.623T>A (p.Ile208Asn) c.449T>A (p.Ile150Asn) | gnomAD v4 |
| 10 | g.119672370T>C | CA378295456 | BAG3 | c.623T>C (p.Ile208Thr) c.449T>C (p.Ile150Thr) | ClinVar dbSNP |
| 10 | g.119672370T>G | CA378295457 | BAG3 | c.623T>G (p.Ile208Ser) c.449T>G (p.Ile150Ser) | |
| 10 | g.119672370T= | CA1940193300 | BAG3 | c.623T= (p.Ile208=) c.449T= (p.Ile150=) | |
| 10 | g.119672371T>A | CA471739760 | BAG3 | c.624T>A (p.Ile208=) c.450T>A (p.Ile150=) | |
| 10 | g.119672371T>C | CA471739761 | BAG3 | c.624T>C (p.Ile208=) c.450T>C (p.Ile150=) | |
| 10 | g.119672371T>G | CA378295458 | BAG3 | c.624T>G (p.Ile208Met) c.450T>G (p.Ile150Met) | COSMIC |
| 10 | g.119672372C>A | CA378295461 | BAG3 | c.625C>A (p.Pro209Thr) c.451C>A (p.Pro151Thr) | |
| 10 | g.119672372C= | CA1940193303 | BAG3 | c.625C= (p.Pro209=) c.451C= (p.Pro151=) | |
| 10 | g.119672372C>G | CA378295460 | BAG3 | c.625C>G (p.Pro209Ala) c.451C>G (p.Pro151Ala) | ClinVar dbSNP |
| 10 | g.119672372C>T | CA378295459 | BAG3 | c.625C>T (p.Pro209Ser) c.451C>T (p.Pro151Ser) | ClinVar dbSNP |
| 10 | g.119672372_119672373delinsTT | CA645568596 | BAG3 | c.625_626delinsTT (p.Pro209Leu) c.451_452delinsTT (p.Pro151Leu) | COSMIC |
| 10 | g.119672373C>A | CA170913 | BAG3 | c.626C>A (p.Pro209Gln) c.452C>A (p.Pro151Gln) | ClinVar dbSNP |
| 10 | g.119672373C= | CA1940193308 | BAG3 | c.626C= (p.Pro209=) c.452C= (p.Pro151=) | |
| 10 | g.119672373C>G | CA378295462 | BAG3 | c.626C>G (p.Pro209Arg) c.452C>G (p.Pro151Arg) | |
| 10 | g.119672373C>T | CA308228 | BAG3 | c.626C>T (p.Pro209Leu) c.452C>T (p.Pro151Leu) | ClinVar dbSNP COSMIC |
| 10 | g.119672374G>A | CA5716385 | BAG3 | c.627G>A (p.Pro209=) c.453G>A (p.Pro151=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672374G>C | CA471739762 | BAG3 | c.627G>C (p.Pro209=) c.453G>C (p.Pro151=) | ClinVar dbSNP |
| 10 | g.119672374G= | CA1940193313 | BAG3 | c.627G= (p.Pro209=) c.453G= (p.Pro151=) | |
| 10 | g.119672374G>T | CA471739763 | BAG3 | c.627G>T (p.Pro209=) c.453G>T (p.Pro151=) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672375G>A | CA378295463 | BAG3 | c.628G>A (p.Val210Met) c.454G>A (p.Val152Met) | |
| 10 | g.119672375G>C | CA378295464 | BAG3 | c.628G>C (p.Val210Leu) c.454G>C (p.Val152Leu) | ClinVar gnomAD v4 |
| 10 | g.119672375G>T | CA378295465 | BAG3 | c.628G>T (p.Val210Leu) c.454G>T (p.Val152Leu) | ClinVar dbSNP |
| 10 | g.119672376T>A | CA378295466 | BAG3 | c.629T>A (p.Val210Glu) c.455T>A (p.Val152Glu) | |
| 10 | g.119672376T>C | CA378295467 | BAG3 | c.629T>C (p.Val210Ala) c.455T>C (p.Val152Ala) | gnomAD v4 |
| 10 | g.119672376T>G | CA378295468 | BAG3 | c.629T>G (p.Val210Gly) c.455T>G (p.Val152Gly) | |
| 10 | g.119672377G>A | CA471739766 | BAG3 | c.630G>A (p.Val210=) c.456G>A (p.Val152=) | |
| 10 | g.119672377G>C | CA471739764 | BAG3 | c.630G>C (p.Val210=) c.456G>C (p.Val152=) | |
| 10 | g.119672377G>T | CA471739765 | BAG3 | c.630G>T (p.Val210=) c.456G>T (p.Val152=) | |
| 10 | g.119672378A>C | CA378295469 | BAG3 | c.631A>C (p.Ile211Leu) c.457A>C (p.Ile153Leu) | |
| 10 | g.119672378A>G | CA378295470 | BAG3 | c.631A>G (p.Ile211Val) c.457A>G (p.Ile153Val) | ClinVar |
| 10 | g.119672378A>T | CA378295471 | BAG3 | c.631A>T (p.Ile211Leu) c.457A>T (p.Ile153Leu) | ClinVar |
| 10 | g.119672379T>A | CA378295474 | BAG3 | c.632T>A (p.Ile211Lys) c.458T>A (p.Ile153Lys) | |
| 10 | g.119672379T>C | CA378295472 | BAG3 | c.632T>C (p.Ile211Thr) c.458T>C (p.Ile153Thr) | |
| 10 | g.119672379T>G | CA378295473 | BAG3 | c.632T>G (p.Ile211Arg) c.458T>G (p.Ile153Arg) | |
| 10 | g.119672380A>C | CA471739768 | BAG3 | c.633A>C (p.Ile211=) c.459A>C (p.Ile153=) | |
| 10 | g.119672380A>G | CA378295475 | BAG3 | c.633A>G (p.Ile211Met) c.459A>G (p.Ile153Met) | |
| 10 | g.119672380A>T | CA471739767 | BAG3 | c.633A>T (p.Ile211=) c.459A>T (p.Ile153=) | |
| 10 | g.119672381C>A | CA378295476 | BAG3 | c.634C>A (p.His212Asn) c.460C>A (p.His154Asn) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672381C= | CA1940193322 | BAG3 | c.634C= (p.His212=) c.460C= (p.His154=) | |
| 10 | g.119672381C>G | CA378295477 | BAG3 | c.634C>G (p.His212Asp) c.460C>G (p.His154Asp) | |
| 10 | g.119672381C>T | CA5716386 | BAG3 | c.634C>T (p.His212Tyr) c.460C>T (p.His154Tyr) | dbSNP ExAC gnomAD v2 |
| 10 | g.119672382A>C | CA378295478 | BAG3 | c.635A>C (p.His212Pro) c.461A>C (p.His154Pro) | |
| 10 | g.119672382A>G | CA378295479 | BAG3 | c.635A>G (p.His212Arg) c.461A>G (p.His154Arg) | |
| 10 | g.119672382A>T | CA378295480 | BAG3 | c.635A>T (p.His212Leu) c.461A>T (p.His154Leu) | |
| 10 | g.119672383C>A | CA378295481 | BAG3 | c.636C>A (p.His212Gln) c.462C>A (p.His154Gln) | |
| 10 | g.119672383C= | CA1940193327 | BAG3 | c.636C= (p.His212=) c.462C= (p.His154=) | |
| 10 | g.119672383C>G | CA378295482 | BAG3 | c.636C>G (p.His212Gln) c.462C>G (p.His154Gln) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.119672383C>T | CA5716387 | BAG3 | c.636C>T (p.His212=) c.462C>T (p.His154=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672384G>A | CA378295483 | BAG3 | c.637G>A (p.Glu213Lys) c.463G>A (p.Glu155Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672384G>C | CA378295484 | BAG3 | c.637G>C (p.Glu213Gln) c.463G>C (p.Glu155Gln) | |
| 10 | g.119672384G= | CA1940193333 | BAG3 | c.637G= (p.Glu213=) c.463G= (p.Glu155=) | |
| 10 | g.119672384G>T | CA378295485 | BAG3 | c.637G>T (p.Glu213Ter) c.463G>T (p.Glu155Ter) | |
| 10 | g.119672385A>C | CA378295487 | BAG3 | c.638A>C (p.Glu213Ala) c.464A>C (p.Glu155Ala) | |
| 10 | g.119672385A>G | CA378295488 | BAG3 | c.638A>G (p.Glu213Gly) c.464A>G (p.Glu155Gly) | |
| 10 | g.119672385A>T | CA378295486 | BAG3 | c.638A>T (p.Glu213Val) c.464A>T (p.Glu155Val) | |
| 10 | g.119672388_119672414del | CA2580082424 | BAG3 | c.641_667del (p.Gln214_Gln222del) c.467_493del (p.Gln156_Gln164del) | ClinVar |
| 10 | g.119672386G>A | CA214221763 | BAG3 | c.639G>A (p.Glu213=) c.465G>A (p.Glu155=) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672386G>C | CA378295490 | BAG3 | c.639G>C (p.Glu213Asp) c.465G>C (p.Glu155Asp) | |
| 10 | g.119672386G= | CA1940193336 | BAG3 | c.639G= (p.Glu213=) c.465G= (p.Glu155=) | |
| 10 | g.119672386G>T | CA378295489 | BAG3 | c.639G>T (p.Glu213Asp) c.465G>T (p.Glu155Asp) | |
| 10 | g.119672387C>A | CA378295492 | BAG3 | c.640C>A (p.Gln214Lys) c.466C>A (p.Gln156Lys) | |
| 10 | g.119672387C>G | CA378295491 | BAG3 | c.640C>G (p.Gln214Glu) c.466C>G (p.Gln156Glu) | |
| 10 | g.119672387C>T | CA378295493 | BAG3 | c.640C>T (p.Gln214Ter) c.466C>T (p.Gln156Ter) | ClinVar dbSNP |
| 10 | g.119672388A>C | CA378295494 | BAG3 | c.641A>C (p.Gln214Pro) c.467A>C (p.Gln156Pro) | |
| 10 | g.119672388A>G | CA378295495 | BAG3 | c.641A>G (p.Gln214Arg) c.467A>G (p.Gln156Arg) | |
| 10 | g.119672388A>T | CA378295496 | BAG3 | c.641A>T (p.Gln214Leu) c.467A>T (p.Gln156Leu) | |
| 10 | g.119672389G>A | CA471739776 | BAG3 | c.642G>A (p.Gln214=) c.468G>A (p.Gln156=) | |
| 10 | g.119672389G>C | CA378295497 | BAG3 | c.642G>C (p.Gln214His) c.468G>C (p.Gln156His) | |
| 10 | g.119672389G>T | CA378295498 | BAG3 | c.642G>T (p.Gln214His) c.468G>T (p.Gln156His) | |
| 10 | g.119672390A>C | CA378295501 | BAG3 | c.643A>C (p.Asn215His) c.469A>C (p.Asn157His) | |
| 10 | g.119672390A>G | CA378295500 | BAG3 | c.643A>G (p.Asn215Asp) c.469A>G (p.Asn157Asp) | |
| 10 | g.119672390A>T | CA378295499 | BAG3 | c.643A>T (p.Asn215Tyr) c.469A>T (p.Asn157Tyr) | |
| 10 | g.119672391A>C | CA378295502 | BAG3 | c.644A>C (p.Asn215Thr) c.470A>C (p.Asn157Thr) | |
| 10 | g.119672391A>G | CA378295503 | BAG3 | c.644A>G (p.Asn215Ser) c.470A>G (p.Asn157Ser) | gnomAD v4 |
| 10 | g.119672391A>T | CA378295504 | BAG3 | c.644A>T (p.Asn215Ile) c.470A>T (p.Asn157Ile) | |
| 10 | g.119672392C>A | CA5716388 | BAG3 | c.645C>A (p.Asn215Lys) c.471C>A (p.Asn157Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672392C= | CA1940193341 | BAG3 | c.645C= (p.Asn215=) c.471C= (p.Asn157=) | |
| 10 | g.119672392C>G | CA378295505 | BAG3 | c.645C>G (p.Asn215Lys) c.471C>G (p.Asn157Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.119672392C>T | CA181168 | BAG3 | c.645C>T (p.Asn215=) c.471C>T (p.Asn157=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.119672393G>A | CA5716389 | BAG3 | c.646G>A (p.Val216Ile) c.472G>A (p.Val158Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672393G>C | CA378295506 | BAG3 | c.646G>C (p.Val216Leu) c.472G>C (p.Val158Leu) | |
| 10 | g.119672393G= | CA1940193351 | BAG3 | c.646G= (p.Val216=) c.472G= (p.Val158=) | |
| 10 | g.119672393G>T | CA237052 | BAG3 | c.646G>T (p.Val216Phe) c.472G>T (p.Val158Phe) | ClinVar dbSNP |
| 10 | g.119672394T>A | CA378295507 | BAG3 | c.647T>A (p.Val216Asp) c.473T>A (p.Val158Asp) | |
| 10 | g.119672394T>C | CA378295508 | BAG3 | c.647T>C (p.Val216Ala) c.473T>C (p.Val158Ala) | |
| 10 | g.119672394T>G | CA378295509 | BAG3 | c.647T>G (p.Val216Gly) c.473T>G (p.Val158Gly) | |
| 10 | g.119672395T>A | CA471739783 | BAG3 | c.648T>A (p.Val216=) c.474T>A (p.Val158=) | |
| 10 | g.119672395T>C | CA471739785 | BAG3 | c.648T>C (p.Val216=) c.474T>C (p.Val158=) | gnomAD v3 gnomAD v4 |
| 10 | g.119672395T>G | CA471739787 | BAG3 | c.648T>G (p.Val216=) c.474T>G (p.Val158=) | |
| 10 | g.119672396A= | CA1940193358 | BAG3 | c.649A= (p.Thr217=) c.475A= (p.Thr159=) | |
| 10 | g.119672396A>C | CA378295510 | BAG3 | c.649A>C (p.Thr217Pro) c.475A>C (p.Thr159Pro) | dbSNP |
| 10 | g.119672396A>G | CA378295511 | BAG3 | c.649A>G (p.Thr217Ala) c.475A>G (p.Thr159Ala) | |
| 10 | g.119672396A>T | CA378295512 | BAG3 | c.649A>T (p.Thr217Ser) c.475A>T (p.Thr159Ser) | |
| 10 | g.119672396_119672397delinsAC | CA1940193357 | BAG3 | c.649_650delinsAC (p.Thr217=) c.475_476delinsAC (p.Thr159=) | |
| 10 | g.119672397C>A | CA378295513 | BAG3 | c.650C>A (p.Thr217Asn) c.476C>A (p.Thr159Asn) | |
| 10 | g.119672397C= | CA1940193362 | BAG3 | c.650C= (p.Thr217=) c.476C= (p.Thr159=) | |
| 10 | g.119672397C>G | CA378295514 | BAG3 | c.650C>G (p.Thr217Ser) c.476C>G (p.Thr159Ser) | |
| 10 | g.119672397C>T | CA378295515 | BAG3 | c.650C>T (p.Thr217Ile) c.476C>T (p.Thr159Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.119672399del | CA16609667 | BAG3 | c.652del (p.Arg218GlyfsTer?) c.478del (p.Arg160GlyfsTer?) | ClinVar dbSNP |
| 10 | g.119672398C>A | CA471739790 | BAG3 | c.651C>A (p.Thr217=) c.477C>A (p.Thr159=) | |
| 10 | g.119672398C= | CA1940193363 | BAG3 | c.651C= (p.Thr217=) c.477C= (p.Thr159=) | |
| 10 | g.119672398C>G | CA471739789 | BAG3 | c.651C>G (p.Thr217=) c.477C>G (p.Thr159=) | |
| 10 | g.119672398C>T | CA214221791 | BAG3 | c.651C>T (p.Thr217=) c.477C>T (p.Thr159=) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672399C>A | CA471739793 | BAG3 | c.652C>A (p.Arg218=) c.478C>A (p.Arg160=) | |
| 10 | g.119672399C= | CA1940193366 | BAG3 | c.652C= (p.Arg218=) c.478C= (p.Arg160=) | |
| 10 | g.119672399C>G | CA378295516 | BAG3 | c.652C>G (p.Arg218Gly) c.478C>G (p.Arg160Gly) | |
| 10 | g.119672399C>T | CA261129 | BAG3 | c.652C>T (p.Arg218Trp) c.478C>T (p.Arg160Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672400G>A | CA183490 | BAG3 | c.653G>A (p.Arg218Gln) c.479G>A (p.Arg160Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672400G>C | CA378295518 | BAG3 | c.653G>C (p.Arg218Pro) c.479G>C (p.Arg160Pro) | |
| 10 | g.119672400G= | CA1940193368 | BAG3 | c.653G= (p.Arg218=) c.479G= (p.Arg160=) | |
| 10 | g.119672400G>T | CA378295517 | BAG3 | c.653G>T (p.Arg218Leu) c.479G>T (p.Arg160Leu) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672401del | CA2499220172 | BAG3 | c.654del (p.Pro219GlnfsTer?) c.480del (p.Pro161GlnfsTer?) | ClinVar dbSNP |
| 10 | g.119672401G>A | CA471739797 | BAG3 | c.654G>A (p.Arg218=) c.480G>A (p.Arg160=) | |
| 10 | g.119672401G>C | CA471739796 | BAG3 | c.654G>C (p.Arg218=) c.480G>C (p.Arg160=) | |
| 10 | g.119672401G>T | CA471739794 | BAG3 | c.654G>T (p.Arg218=) c.480G>T (p.Arg160=) | |
| 10 | g.119672402C>A | CA378295519 | BAG3 | c.655C>A (p.Pro219Thr) c.481C>A (p.Pro161Thr) | |
| 10 | g.119672402C= | CA1940193373 | BAG3 | c.655C= (p.Pro219=) c.481C= (p.Pro161=) | |
| 10 | g.119672402C>G | CA378295520 | BAG3 | c.655C>G (p.Pro219Ala) c.481C>G (p.Pro161Ala) | |
| 10 | g.119672402C>T | CA378295521 | BAG3 | c.655C>T (p.Pro219Ser) c.481C>T (p.Pro161Ser) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672403C>A | CA378295522 | BAG3 | c.656C>A (p.Pro219Gln) c.482C>A (p.Pro161Gln) | |
| 10 | g.119672403C>G | CA378295523 | BAG3 | c.656C>G (p.Pro219Arg) c.482C>G (p.Pro161Arg) | |
| 10 | g.119672403C>T | CA378295524 | BAG3 | c.656C>T (p.Pro219Leu) c.482C>T (p.Pro161Leu) | gnomAD v4 |
| 10 | g.119672404A= | CA1940193374 | BAG3 | c.657A= (p.Pro219=) c.483A= (p.Pro161=) | |
| 10 | g.119672404A>C | CA471739799 | BAG3 | c.657A>C (p.Pro219=) c.483A>C (p.Pro161=) | |
| 10 | g.119672404A>G | CA471739802 | BAG3 | c.657A>G (p.Pro219=) c.483A>G (p.Pro161=) | dbSNP |
| 10 | g.119672404A>T | CA471739800 | BAG3 | c.657A>T (p.Pro219=) c.483A>T (p.Pro161=) | |
| 10 | g.119672405G>A | CA378295525 | BAG3 | c.658G>A (p.Ala220Thr) c.484G>A (p.Ala162Thr) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672405G>C | CA378295526 | BAG3 | c.658G>C (p.Ala220Pro) c.484G>C (p.Ala162Pro) | dbSNP |
| 10 | g.119672405G= | CA1940193375 | BAG3 | c.658G= (p.Ala220=) c.484G= (p.Ala162=) | |
| 10 | g.119672405G>T | CA378295527 | BAG3 | c.658G>T (p.Ala220Ser) c.484G>T (p.Ala162Ser) | |
| 10 | g.119672406C>A | CA378295528 | BAG3 | c.659C>A (p.Ala220Glu) c.485C>A (p.Ala162Glu) | |
| 10 | g.119672406C>G | CA378295529 | BAG3 | c.659C>G (p.Ala220Gly) c.485C>G (p.Ala162Gly) | |
| 10 | g.119672406C>T | CA378295530 | BAG3 | c.659C>T (p.Ala220Val) c.485C>T (p.Ala162Val) | |
| 10 | g.119672407A>C | CA471739806 | BAG3 | c.660A>C (p.Ala220=) c.486A>C (p.Ala162=) | |
| 10 | g.119672407A>G | CA471739807 | BAG3 | c.660A>G (p.Ala220=) c.486A>G (p.Ala162=) | |
| 10 | g.119672407A>T | CA471739809 | BAG3 | c.660A>T (p.Ala220=) c.486A>T (p.Ala162=) | |
| 10 | g.119672408G>A | CA378295533 | BAG3 | c.661G>A (p.Ala221Thr) c.487G>A (p.Ala163Thr) | gnomAD v4 |
| 10 | g.119672408G>C | CA378295531 | BAG3 | c.661G>C (p.Ala221Pro) c.487G>C (p.Ala163Pro) | |
| 10 | g.119672408G>T | CA378295532 | BAG3 | c.661G>T (p.Ala221Ser) c.487G>T (p.Ala163Ser) | |
| 10 | g.119672409C>A | CA378295534 | BAG3 | c.662C>A (p.Ala221Asp) c.488C>A (p.Ala163Asp) | |
| 10 | g.119672409C>G | CA378295535 | BAG3 | c.662C>G (p.Ala221Gly) c.488C>G (p.Ala163Gly) | |
| 10 | g.119672409C>T | CA378295536 | BAG3 | c.662C>T (p.Ala221Val) c.488C>T (p.Ala163Val) | ClinVar gnomAD v4 |
| 10 | g.119672410C>A | CA471739814 | BAG3 | c.663C>A (p.Ala221=) c.489C>A (p.Ala163=) | |
| 10 | g.119672410C>G | CA471739816 | BAG3 | c.663C>G (p.Ala221=) c.489C>G (p.Ala163=) | gnomAD v4 |
| 10 | g.119672410C>T | CA471739818 | BAG3 | c.663C>T (p.Ala221=) c.489C>T (p.Ala163=) | ClinVar |
| 10 | g.119672411C>A | CA378295537 | BAG3 | c.664C>A (p.Gln222Lys) c.490C>A (p.Gln164Lys) | |
| 10 | g.119672411C>G | CA378295538 | BAG3 | c.664C>G (p.Gln222Glu) c.490C>G (p.Gln164Glu) | |
| 10 | g.119672411C>T | CA378295539 | BAG3 | c.664C>T (p.Gln222Ter) c.490C>T (p.Gln164Ter) | |
| 10 | g.119672412A>C | CA378295540 | BAG3 | c.665A>C (p.Gln222Pro) c.491A>C (p.Gln164Pro) | |
| 10 | g.119672412A>G | CA378295541 | BAG3 | c.665A>G (p.Gln222Arg) c.491A>G (p.Gln164Arg) | ClinVar |
| 10 | g.119672412A>T | CA378295542 | BAG3 | c.665A>T (p.Gln222Leu) c.491A>T (p.Gln164Leu) | |
| 10 | g.119672413G>A | CA471739823 | BAG3 | c.666G>A (p.Gln222=) c.492G>A (p.Gln164=) | |
| 10 | g.119672413G>C | CA378295543 | BAG3 | c.666G>C (p.Gln222His) c.492G>C (p.Gln164His) | |
| 10 | g.119672413G= | CA1940193376 | BAG3 | c.666G= (p.Gln222=) c.492G= (p.Gln164=) | |
| 10 | g.119672413G>T | CA378295544 | BAG3 | c.666G>T (p.Gln222His) c.492G>T (p.Gln164His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672414C>A | CA378295546 | BAG3 | c.667C>A (p.Pro223Thr) c.493C>A (p.Pro165Thr) | ClinVar dbSNP gnomAD v4 |
| 10 | g.119672414C= | CA1940193379 | BAG3 | c.667C= (p.Pro223=) c.493C= (p.Pro165=) | |
| 10 | g.119672414C>G | CA378295547 | BAG3 | c.667C>G (p.Pro223Ala) c.493C>G (p.Pro165Ala) | ClinVar gnomAD v4 |
| 10 | g.119672414C>T | CA378295545 | BAG3 | c.667C>T (p.Pro223Ser) c.493C>T (p.Pro165Ser) | |
| 10 | g.119672415C>A | CA378295548 | BAG3 | c.668C>A (p.Pro223His) c.494C>A (p.Pro165His) | |
| 10 | g.119672415C= | CA1940193385 | BAG3 | c.668C= (p.Pro223=) c.494C= (p.Pro165=) | |
| 10 | g.119672415C>G | CA077630 | BAG3 | c.668C>G (p.Pro223Arg) c.494C>G (p.Pro165Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.119672415C>T | CA5716390 | BAG3 | c.668C>T (p.Pro223Leu) c.494C>T (p.Pro165Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672416C>A | CA471739831 | BAG3 | c.669C>A (p.Pro223=) c.495C>A (p.Pro165=) | |
| 10 | g.119672416C= | CA1940193386 | BAG3 | c.669C= (p.Pro223=) c.495C= (p.Pro165=) | |
| 10 | g.119672416C>G | CA471739833 | BAG3 | c.669C>G (p.Pro223=) c.495C>G (p.Pro165=) | |
| 10 | g.119672416C>T | CA5716391 | BAG3 | c.669C>T (p.Pro223=) c.495C>T (p.Pro165=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.119672417del | CA2695212862 | BAG3 | c.670del (p.Ser224ProfsTer?) c.496del (p.Ser166ProfsTer?) | |
| 10 | g.119672417T>A | CA378295549 | BAG3 | c.670T>A (p.Ser224Thr) c.496T>A (p.Ser166Thr) | |
| 10 | g.119672417T>C | CA378295550 | BAG3 | c.670T>C (p.Ser224Pro) c.496T>C (p.Ser166Pro) | |
| 10 | g.119672417T>G | CA378295551 | BAG3 | c.670T>G (p.Ser224Ala) c.496T>G (p.Ser166Ala) | |
| 10 | g.119672417dup | CA645372886 | BAG3 | c.670dup (p.Ser224PhefsTer?) c.496dup (p.Ser166PhefsTer?) | ClinVar dbSNP |
| 10 | g.119672418C>A | CA378295552 | BAG3 | c.671C>A (p.Ser224Tyr) c.497C>A (p.Ser166Tyr) | |
| 10 | g.119672418C>G | CA378295554 | BAG3 | c.671C>G (p.Ser224Cys) c.497C>G (p.Ser166Cys) | |
| 10 | g.119672418C>T | CA378295553 | BAG3 | c.671C>T (p.Ser224Phe) c.497C>T (p.Ser166Phe) | |
| 10 | g.119672419C>A | CA471739838 | BAG3 | c.672C>A (p.Ser224=) c.498C>A (p.Ser166=) | |
| 10 | g.119672419C= | CA1940193387 | BAG3 | c.672C= (p.Ser224=) c.498C= (p.Ser166=) | |
| 10 | g.119672419C>G | CA471739839 | BAG3 | c.672C>G (p.Ser224=) c.498C>G (p.Ser166=) | |
| 10 | g.119672419C>T | CA5716392 | BAG3 | c.672C>T (p.Ser224=) c.498C>T (p.Ser166=) | dbSNP ExAC gnomAD v2 gnomAD v4 |