Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.119677754C>A | CA383282091 | NECTIN1 | c.534G>T (p.Lys178Asn) n.508G>T | |
11 | g.119677754C>G | CA383282092 | NECTIN1 | c.534G>C (p.Lys178Asn) n.508G>C | |
11 | g.119677754C>T | CA477265351 | NECTIN1 | c.534G>A (p.Lys178=) n.508G>A | |
11 | g.119677755T>A | CA383282093 | NECTIN1 | c.533A>T (p.Lys178Met) n.507A>T | |
11 | g.119677755T>C | CA383282094 | NECTIN1 | c.533A>G (p.Lys178Arg) n.507A>G | |
11 | g.119677755T>G | CA383282095 | NECTIN1 | c.533A>C (p.Lys178Thr) n.507A>C | |
11 | g.119677756T>A | CA383282097 | NECTIN1 | c.532A>T (p.Lys178Ter) n.506A>T | |
11 | g.119677756T>C | CA383282098 | NECTIN1 | c.532A>G (p.Lys178Glu) n.506A>G | |
11 | g.119677756T>G | CA383282096 | NECTIN1 | c.532A>C (p.Lys178Gln) n.506A>C | |
11 | g.119677757C>A | CA477265371 | NECTIN1 | c.531G>T (p.Gly177=) n.505G>T | |
11 | g.119677757C>G | CA477265377 | NECTIN1 | c.531G>C (p.Gly177=) n.505G>C | |
11 | g.119677757C>T | CA477265392 | NECTIN1 | c.531G>A (p.Gly177=) n.505G>A | |
11 | g.119677758C>A | CA383282100 | NECTIN1 | c.530G>T (p.Gly177Val) n.504G>T | |
11 | g.119677758C>G | CA383282099 | NECTIN1 | c.530G>C (p.Gly177Ala) n.504G>C | |
11 | g.119677758C>T | CA383282101 | NECTIN1 | c.530G>A (p.Gly177Glu) n.504G>A | |
11 | g.119677759C>A | CA383282102 | NECTIN1 | c.529G>T (p.Gly177Trp) n.503G>T | |
11 | g.119677759C>G | CA383282104 | NECTIN1 | c.529G>C (p.Gly177Arg) n.503G>C | |
11 | g.119677759C>T | CA383282103 | NECTIN1 | c.529G>A (p.Gly177Arg) n.503G>A | COSMIC COSMIC COSMIC |
11 | g.119677760A>C | CA383282105 | NECTIN1 | c.528T>G (p.Asn176Lys) n.502T>G | |
11 | g.119677760A>G | CA477265407 | NECTIN1 | c.528T>C (p.Asn176=) n.502T>C | gnomAD v4 |
11 | g.119677760A>T | CA383282106 | NECTIN1 | c.528T>A (p.Asn176Lys) n.502T>A | |
11 | g.119677761T>A | CA383282107 | NECTIN1 | c.527A>T (p.Asn176Ile) n.501A>T | |
11 | g.119677761T>C | CA6322062 | NECTIN1 | c.527A>G (p.Asn176Ser) n.501A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
11 | g.119677761T>G | CA383282108 | NECTIN1 | c.527A>C (p.Asn176Thr) n.501A>C | |
11 | g.119677761T= | CA2004079103 | NECTIN1 | c.527A= (p.Asn176=) n.501A= | |
11 | g.119677762T>A | CA383282109 | NECTIN1 | c.526A>T (p.Asn176Tyr) n.500A>T | |
11 | g.119677762T>C | CA383282110 | NECTIN1 | c.526A>G (p.Asn176Asp) n.500A>G | |
11 | g.119677762T>G | CA383282111 | NECTIN1 | c.526A>C (p.Asn176His) n.500A>C | |
11 | g.119677763G>A | CA477265436 | NECTIN1 | c.525C>T (p.Ala175=) n.499C>T | |
11 | g.119677763G>C | CA477265439 | NECTIN1 | c.525C>G (p.Ala175=) n.499C>G | |
11 | g.119677763G>T | CA477265441 | NECTIN1 | c.525C>A (p.Ala175=) n.499C>A | |
11 | g.119677764G>A | CA383282112 | NECTIN1 | c.524C>T (p.Ala175Val) n.498C>T | gnomAD v4 |
11 | g.119677764G>C | CA383282113 | NECTIN1 | c.524C>G (p.Ala175Gly) n.498C>G | gnomAD v4 |
11 | g.119677764G>T | CA383282114 | NECTIN1 | c.524C>A (p.Ala175Asp) n.498C>A | |
11 | g.119677765C>A | CA383282115 | NECTIN1 | c.523G>T (p.Ala175Ser) n.497G>T | |
11 | g.119677765C= | CA2004079106 | NECTIN1 | c.523G= (p.Ala175=) n.497G= | |
11 | g.119677765C>G | CA383282117 | NECTIN1 | c.523G>C (p.Ala175Pro) n.497G>C | |
11 | g.119677765C>T | CA383282116 | NECTIN1 | c.523G>A (p.Ala175Thr) n.497G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.119677766T>A | CA477265466 | NECTIN1 | c.522A>T (p.Ser174=) n.496A>T | |
11 | g.119677766T>C | CA477265469 | NECTIN1 | c.522A>G (p.Ser174=) n.496A>G | |
11 | g.119677766T>G | CA477265475 | NECTIN1 | c.522A>C (p.Ser174=) n.496A>C | |
11 | g.119677767G>A | CA383282118 | NECTIN1 | c.521C>T (p.Ser174Leu) n.495C>T | dbSNP COSMIC COSMIC COSMIC |
11 | g.119677767G>C | CA383282119 | NECTIN1 | c.521C>G (p.Ser174Ter) n.495C>G | |
11 | g.119677767G= | CA2004079112 | NECTIN1 | c.521C= (p.Ser174=) n.495C= | |
11 | g.119677767G>T | CA383282120 | NECTIN1 | c.521C>A (p.Ser174Ter) n.495C>A | |
11 | g.119677768A>C | CA383282121 | NECTIN1 | c.520T>G (p.Ser174Ala) n.494T>G | |
11 | g.119677768A>G | CA383282122 | NECTIN1 | c.520T>C (p.Ser174Pro) n.494T>C | gnomAD v4 |
11 | g.119677768A>T | CA383282123 | NECTIN1 | c.520T>A (p.Ser174Thr) n.494T>A | |
11 | g.119677769G>A | CA477265497 | NECTIN1 | c.519C>T (p.Thr173=) n.493C>T | dbSNP |
11 | g.119677769G>C | CA477265496 | NECTIN1 | c.519C>G (p.Thr173=) n.493C>G | |
11 | g.119677769G>T | CA477265495 | NECTIN1 | c.519C>A (p.Thr173=) n.493C>A | |
11 | g.119677770G>A | CA383282124 | NECTIN1 | c.518C>T (p.Thr173Ile) n.492C>T | |
11 | g.119677770G>C | CA383282125 | NECTIN1 | c.518C>G (p.Thr173Ser) n.492C>G | gnomAD v4 |
11 | g.119677770G>T | CA383282126 | NECTIN1 | c.518C>A (p.Thr173Asn) n.492C>A | gnomAD v4 |
11 | g.119677771T>A | CA383282128 | NECTIN1 | c.517A>T (p.Thr173Ser) n.491A>T | |
11 | g.119677771T>C | CA383282129 | NECTIN1 | c.517A>G (p.Thr173Ala) n.491A>G | |
11 | g.119677771T>G | CA383282127 | NECTIN1 | c.517A>C (p.Thr173Pro) n.491A>C | dbSNP |
11 | g.119677771T= | CA2004079116 | NECTIN1 | c.517A= (p.Thr173=) n.491A= | |
11 | g.119677772G>A | CA477265519 | NECTIN1 | c.516C>T (p.Cys172=) n.490C>T | gnomAD v4 |
11 | g.119677772G>C | CA383282130 | NECTIN1 | c.516C>G (p.Cys172Trp) n.490C>G | |
11 | g.119677772G>T | CA383282131 | NECTIN1 | c.516C>A (p.Cys172Ter) n.490C>A | |
11 | g.119677773C>A | CA383282132 | NECTIN1 | c.515G>T (p.Cys172Phe) n.489G>T | |
11 | g.119677773C>G | CA383282133 | NECTIN1 | c.515G>C (p.Cys172Ser) n.489G>C | gnomAD v4 |
11 | g.119677773C>T | CA383282134 | NECTIN1 | c.515G>A (p.Cys172Tyr) n.489G>A | gnomAD v4 |
11 | g.119677774A>C | CA383282135 | NECTIN1 | c.514T>G (p.Cys172Gly) n.488T>G | |
11 | g.119677774A>G | CA383282136 | NECTIN1 | c.514T>C (p.Cys172Arg) n.488T>C | |
11 | g.119677774A>T | CA383282137 | NECTIN1 | c.514T>A (p.Cys172Ser) n.488T>A | gnomAD v4 |
11 | g.119677775G>A | CA477265543 | NECTIN1 | c.513C>T (p.Thr171=) n.487C>T | |
11 | g.119677775G>C | CA477265551 | NECTIN1 | c.513C>G (p.Thr171=) n.487C>G | |
11 | g.119677775G>T | CA477265550 | NECTIN1 | c.513C>A (p.Thr171=) n.487C>A | gnomAD v4 |
11 | g.119677776G>A | CA6322063 | NECTIN1 | c.512C>T (p.Thr171Ile) n.486C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677776G>C | CA383282138 | NECTIN1 | c.512C>G (p.Thr171Ser) n.486C>G | |
11 | g.119677776G= | CA2004079123 | NECTIN1 | c.512C= (p.Thr171=) n.486C= | |
11 | g.119677776G>T | CA383282139 | NECTIN1 | c.512C>A (p.Thr171Asn) n.486C>A | |
11 | g.119677777T>A | CA383282141 | NECTIN1 | c.511A>T (p.Thr171Ser) n.485A>T | |
11 | g.119677777T>C | CA383282142 | NECTIN1 | c.511A>G (p.Thr171Ala) n.485A>G | gnomAD v4 |
11 | g.119677777T>G | CA383282140 | NECTIN1 | c.511A>C (p.Thr171Pro) n.485A>C | dbSNP |
11 | g.119677777T= | CA2004079126 | NECTIN1 | c.511A= (p.Thr171=) n.485A= | |
11 | g.119677778G>A | CA477265572 | NECTIN1 | c.510C>T (p.Ala170=) n.484C>T | |
11 | g.119677778G>C | CA477265575 | NECTIN1 | c.510C>G (p.Ala170=) n.484C>G | |
11 | g.119677778G>T | CA477265580 | NECTIN1 | c.510C>A (p.Ala170=) n.484C>A | |
11 | g.119677779G>A | CA383282143 | NECTIN1 | c.509C>T (p.Ala170Val) n.483C>T | dbSNP gnomAD v4 COSMIC COSMIC COSMIC |
11 | g.119677779G>C | CA383282144 | NECTIN1 | c.509C>G (p.Ala170Gly) n.483C>G | |
11 | g.119677779G= | CA2004079130 | NECTIN1 | c.509C= (p.Ala170=) n.483C= | |
11 | g.119677779G>T | CA383282145 | NECTIN1 | c.509C>A (p.Ala170Asp) n.483C>A | |
11 | g.119677780C>A | CA383282146 | NECTIN1 | c.508G>T (p.Ala170Ser) n.482G>T | |
11 | g.119677780C>G | CA383282147 | NECTIN1 | c.508G>C (p.Ala170Pro) n.482G>C | |
11 | g.119677780C>T | CA383282148 | NECTIN1 | c.508G>A (p.Ala170Thr) n.482G>A | gnomAD v4 |
11 | g.119677781C>A | CA477265606 | NECTIN1 | c.507G>T (p.Val169=) n.481G>T | |
11 | g.119677781C>G | CA477265597 | NECTIN1 | c.507G>C (p.Val169=) n.481G>C | |
11 | g.119677781C>T | CA477265600 | NECTIN1 | c.507G>A (p.Val169=) n.481G>A | |
11 | g.119677782A>C | CA383282149 | NECTIN1 | c.506T>G (p.Val169Gly) n.480T>G | |
11 | g.119677782A>G | CA383282151 | NECTIN1 | c.506T>C (p.Val169Ala) n.480T>C | |
11 | g.119677782A>T | CA383282150 | NECTIN1 | c.506T>A (p.Val169Glu) n.480T>A | |
11 | g.119677783C>A | CA383282152 | NECTIN1 | c.505G>T (p.Val169Leu) n.479G>T | dbSNP |
11 | g.119677783C= | CA2004079134 | NECTIN1 | c.505G= (p.Val169=) n.479G= | |
11 | g.119677783C>G | CA383282153 | NECTIN1 | c.505G>C (p.Val169Leu) n.479G>C | |
11 | g.119677783C>T | CA383282154 | NECTIN1 | c.505G>A (p.Val169Met) n.479G>A | |
11 | g.119677784C>A | CA477265635 | NECTIN1 | c.504G>T (p.Leu168=) n.478G>T | |
11 | g.119677784C= | CA2004079141 | NECTIN1 | c.504G= (p.Leu168=) n.478G= | |
11 | g.119677784C>G | CA6322065 | NECTIN1 | c.504G>C (p.Leu168=) n.478G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677784C>T | CA6322064 | NECTIN1 | c.504G>A (p.Leu168=) n.478G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677785A>C | CA383282156 | NECTIN1 | c.503T>G (p.Leu168Arg) n.477T>G | |
11 | g.119677785A>G | CA383282157 | NECTIN1 | c.503T>C (p.Leu168Pro) n.477T>C | |
11 | g.119677785A>T | CA383282155 | NECTIN1 | c.503T>A (p.Leu168Gln) n.477T>A | |
11 | g.119677786G>A | CA6322066 | NECTIN1 | c.502C>T (p.Leu168=) n.476C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677786G>C | CA383282158 | NECTIN1 | c.502C>G (p.Leu168Val) n.476C>G | |
11 | g.119677786G= | CA2004079145 | NECTIN1 | c.502C= (p.Leu168=) n.476C= | |
11 | g.119677786G>T | CA383282159 | NECTIN1 | c.502C>A (p.Leu168Met) n.476C>A | |
11 | g.119677787G>A | CA477265649 | NECTIN1 | c.501C>T (p.Val167=) n.475C>T | |
11 | g.119677787G>C | CA477265646 | NECTIN1 | c.501C>G (p.Val167=) n.475C>G | |
11 | g.119677787G>T | CA477265648 | NECTIN1 | c.501C>A (p.Val167=) n.475C>A | |
11 | g.119677788A= | CA2004079153 | NECTIN1 | c.500T= (p.Val167=) n.474T= | |
11 | g.119677788A>C | CA383282160 | NECTIN1 | c.500T>G (p.Val167Gly) n.474T>G | dbSNP |
11 | g.119677788A>G | CA383282161 | NECTIN1 | c.500T>C (p.Val167Ala) n.474T>C | gnomAD v4 |
11 | g.119677788A>T | CA383282162 | NECTIN1 | c.500T>A (p.Val167Asp) n.474T>A | |
11 | g.119677789C>A | CA383282164 | NECTIN1 | c.499G>T (p.Val167Phe) n.473G>T | |
11 | g.119677789C= | CA2004079158 | NECTIN1 | c.499G= (p.Val167=) n.473G= | |
11 | g.119677789C>G | CA383282163 | NECTIN1 | c.499G>C (p.Val167Leu) n.473G>C | |
11 | g.119677789C>T | CA229370381 | NECTIN1 | c.499G>A (p.Val167Ile) n.473G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.119677790C>A | CA383282165 | NECTIN1 | c.498G>T (p.Lys166Asn) n.472G>T | |
11 | g.119677790C>G | CA383282166 | NECTIN1 | c.498G>C (p.Lys166Asn) n.472G>C | |
11 | g.119677790C>T | CA477265674 | NECTIN1 | c.498G>A (p.Lys166=) n.472G>A | |
11 | g.119677791T>A | CA383282167 | NECTIN1 | c.497A>T (p.Lys166Met) n.471A>T | |
11 | g.119677791T>C | CA383282168 | NECTIN1 | c.497A>G (p.Lys166Arg) n.471A>G | |
11 | g.119677791T>G | CA383282169 | NECTIN1 | c.497A>C (p.Lys166Thr) n.471A>C | |
11 | g.119677792T>A | CA383282171 | NECTIN1 | c.496A>T (p.Lys166Ter) n.470A>T | |
11 | g.119677792T>C | CA383282170 | NECTIN1 | c.496A>G (p.Lys166Glu) n.470A>G | dbSNP gnomAD v3 gnomAD v4 |
11 | g.119677792T>G | CA229370386 | NECTIN1 | c.496A>C (p.Lys166Gln) n.470A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677792T= | CA2004079163 | NECTIN1 | c.496A= (p.Lys166=) n.470A= | |
11 | g.119677793G>A | CA477265702 | NECTIN1 | c.495C>T (p.Asp165=) n.469C>T | |
11 | g.119677793G>C | CA383282172 | NECTIN1 | c.495C>G (p.Asp165Glu) n.469C>G | |
11 | g.119677793G= | CA2004079167 | NECTIN1 | c.495C= (p.Asp165=) n.469C= | |
11 | g.119677793G>T | CA6322067 | NECTIN1 | c.495C>A (p.Asp165Glu) n.469C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677794T>A | CA383282173 | NECTIN1 | c.494A>T (p.Asp165Val) n.468A>T | |
11 | g.119677794T>C | CA383282174 | NECTIN1 | c.494A>G (p.Asp165Gly) n.468A>G | |
11 | g.119677794T>G | CA383282175 | NECTIN1 | c.494A>C (p.Asp165Ala) n.468A>C | |
11 | g.119677795C>A | CA383282176 | NECTIN1 | c.493G>T (p.Asp165Tyr) n.467G>T | |
11 | g.119677795C>G | CA383282177 | NECTIN1 | c.493G>C (p.Asp165His) n.467G>C | |
11 | g.119677795C>T | CA383282178 | NECTIN1 | c.493G>A (p.Asp165Asn) n.467G>A | |
11 | g.119677796A>C | CA383282179 | NECTIN1 | c.492T>G (p.Asp164Glu) n.466T>G | |
11 | g.119677796A>G | CA477265746 | NECTIN1 | c.492T>C (p.Asp164=) n.466T>C | |
11 | g.119677796A>T | CA383282180 | NECTIN1 | c.492T>A (p.Asp164Glu) n.466T>A | |
11 | g.119677797T>A | CA383282181 | NECTIN1 | c.491A>T (p.Asp164Val) n.465A>T | |
11 | g.119677797T>C | CA383282182 | NECTIN1 | c.491A>G (p.Asp164Gly) n.465A>G | |
11 | g.119677797T>G | CA383282183 | NECTIN1 | c.491A>C (p.Asp164Ala) n.465A>C | |
11 | g.119677798C>A | CA383282184 | NECTIN1 | c.490G>T (p.Asp164Tyr) n.464G>T | dbSNP |
11 | g.119677798C= | CA2004079170 | NECTIN1 | c.490G= (p.Asp164=) n.464G= | |
11 | g.119677798C>G | CA383282186 | NECTIN1 | c.490G>C (p.Asp164His) n.464G>C | |
11 | g.119677798C>T | CA383282185 | NECTIN1 | c.490G>A (p.Asp164Asn) n.464G>A | gnomAD v4 |
11 | g.119677799C>A | CA383282187 | NECTIN1 | c.489G>T (p.Gln163His) n.463G>T | |
11 | g.119677799C>G | CA383282188 | NECTIN1 | c.489G>C (p.Gln163His) n.463G>C | |
11 | g.119677799C>T | CA477265782 | NECTIN1 | c.489G>A (p.Gln163=) n.463G>A | gnomAD v4 |
11 | g.119677800T>A | CA383282189 | NECTIN1 | c.488A>T (p.Gln163Leu) n.462A>T | |
11 | g.119677800T>C | CA383282190 | NECTIN1 | c.488A>G (p.Gln163Arg) n.462A>G | |
11 | g.119677800T>G | CA383282191 | NECTIN1 | c.488A>C (p.Gln163Pro) n.462A>C | dbSNP gnomAD v4 |
11 | g.119677800T= | CA2004079173 | NECTIN1 | c.488A= (p.Gln163=) n.462A= | |
11 | g.119677801G>A | CA383282192 | NECTIN1 | c.487C>T (p.Gln163Ter) n.461C>T | |
11 | g.119677801G>C | CA383282193 | NECTIN1 | c.487C>G (p.Gln163Glu) n.461C>G | |
11 | g.119677801G>T | CA383282194 | NECTIN1 | c.487C>A (p.Gln163Lys) n.461C>A | |
11 | g.119677802C>A | CA477265801 | NECTIN1 | c.486G>T (p.Gly162=) n.460G>T | |
11 | g.119677802C= | CA2004079175 | NECTIN1 | c.486G= (p.Gly162=) n.460G= | |
11 | g.119677802C>G | CA477265802 | NECTIN1 | c.486G>C (p.Gly162=) n.460G>C | |
11 | g.119677802C>T | CA477265805 | NECTIN1 | c.486G>A (p.Gly162=) n.460G>A | dbSNP |
11 | g.119677803C>A | CA383282195 | NECTIN1 | c.485G>T (p.Gly162Val) n.459G>T | COSMIC COSMIC COSMIC |
11 | g.119677803C= | CA2004079180 | NECTIN1 | c.485G= (p.Gly162=) n.459G= | |
11 | g.119677803C>G | CA383282196 | NECTIN1 | c.485G>C (p.Gly162Ala) n.459G>C | |
11 | g.119677803C>T | CA6322068 | NECTIN1 | c.485G>A (p.Gly162Glu) n.459G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677804C>A | CA383282197 | NECTIN1 | c.484G>T (p.Gly162Trp) n.458G>T | |
11 | g.119677804C>G | CA383282198 | NECTIN1 | c.484G>C (p.Gly162Arg) n.458G>C | |
11 | g.119677804C>T | CA383282199 | NECTIN1 | c.484G>A (p.Gly162Arg) n.458G>A | gnomAD v4 |
11 | g.119677805C>A | CA383282200 | NECTIN1 | c.483G>T (p.Lys161Asn) n.457G>T | |
11 | g.119677805C= | CA2004079185 | NECTIN1 | c.483G= (p.Lys161=) n.457G= | |
11 | g.119677805C>G | CA6322069 | NECTIN1 | c.483G>C (p.Lys161Asn) n.457G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677805C>T | CA477265831 | NECTIN1 | c.483G>A (p.Lys161=) n.457G>A | |
11 | g.119677806T>A | CA383282201 | NECTIN1 | c.482A>T (p.Lys161Met) n.456A>T | |
11 | g.119677806T>C | CA383282202 | NECTIN1 | c.482A>G (p.Lys161Arg) n.456A>G | |
11 | g.119677806T>G | CA383282203 | NECTIN1 | c.482A>C (p.Lys161Thr) n.456A>C | gnomAD v4 |
11 | g.119677807T>A | CA383282204 | NECTIN1 | c.481A>T (p.Lys161Ter) n.455A>T | |
11 | g.119677807T>C | CA383282205 | NECTIN1 | c.481A>G (p.Lys161Glu) n.455A>G | |
11 | g.119677807T>G | CA383282206 | NECTIN1 | c.481A>C (p.Lys161Gln) n.455A>C | |
11 | g.119677808C>A | CA383282207 | NECTIN1 | c.480G>T (p.Lys160Asn) n.454G>T | |
11 | g.119677808C= | CA2004079191 | NECTIN1 | c.480G= (p.Lys160=) n.454G= | |
11 | g.119677808C>G | CA6322071 | NECTIN1 | c.480G>C (p.Lys160Asn) n.454G>C | dbSNP ExAC gnomAD v3 gnomAD v4 |
11 | g.119677808C>T | CA6322070 | NECTIN1 | c.480G>A (p.Lys160=) n.454G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677809T>A | CA383282208 | NECTIN1 | c.479A>T (p.Lys160Met) n.453A>T | |
11 | g.119677809T>C | CA383282209 | NECTIN1 | c.479A>G (p.Lys160Arg) n.453A>G | |
11 | g.119677809T>G | CA383282210 | NECTIN1 | c.479A>C (p.Lys160Thr) n.453A>C | |
11 | g.119677810T>A | CA383282212 | NECTIN1 | c.478A>T (p.Lys160Ter) n.452A>T | |
11 | g.119677810T>C | CA383282213 | NECTIN1 | c.478A>G (p.Lys160Glu) n.452A>G | |
11 | g.119677810T>G | CA383282211 | NECTIN1 | c.478A>C (p.Lys160Gln) n.452A>C | |
11 | g.119677811G>A | CA477265912 | NECTIN1 | c.477C>T (p.Ala159=) n.451C>T | |
11 | g.119677811G>C | CA477265916 | NECTIN1 | c.477C>G (p.Ala159=) n.451C>G | |
11 | g.119677811G>T | CA477265920 | NECTIN1 | c.477C>A (p.Ala159=) n.451C>A | |
11 | g.119677812G>A | CA383282216 | NECTIN1 | c.476C>T (p.Ala159Val) n.450C>T | gnomAD v4 |
11 | g.119677812G>C | CA383282214 | NECTIN1 | c.476C>G (p.Ala159Gly) n.450C>G | gnomAD v4 |
11 | g.119677812G= | CA2004079198 | NECTIN1 | c.476C= (p.Ala159=) n.450C= | |
11 | g.119677812G>T | CA383282215 | NECTIN1 | c.476C>A (p.Ala159Asp) n.450C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.119677813C>A | CA383282217 | NECTIN1 | c.475G>T (p.Ala159Ser) n.449G>T | |
11 | g.119677813C>G | CA383282218 | NECTIN1 | c.475G>C (p.Ala159Pro) n.449G>C | |
11 | g.119677813C>T | CA383282219 | NECTIN1 | c.475G>A (p.Ala159Thr) n.449G>A | |
11 | g.119677814T>A | CA477265938 | NECTIN1 | c.474A>T (p.Arg158=) n.448A>T | |
11 | g.119677814T>C | CA477265941 | NECTIN1 | c.474A>G (p.Arg158=) n.448A>G | |
11 | g.119677814T>G | CA477265943 | NECTIN1 | c.474A>C (p.Arg158=) n.448A>C | |
11 | g.119677815C>A | CA383282220 | NECTIN1 | c.473G>T (p.Arg158Leu) n.447G>T | |
11 | g.119677815C= | CA2004079202 | NECTIN1 | c.473G= (p.Arg158=) n.447G= | |
11 | g.119677815C>G | CA6322073 | NECTIN1 | c.473G>C (p.Arg158Pro) n.447G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677815C>T | CA6322072 | NECTIN1 | c.473G>A (p.Arg158Gln) n.447G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677816G>A | CA383282221 | NECTIN1 | c.472C>T (p.Arg158Ter) n.446C>T | ClinVar dbSNP gnomAD v4 |
11 | g.119677816G>C | CA383282222 | NECTIN1 | c.472C>G (p.Arg158Gly) n.446C>G | |
11 | g.119677816G>T | CA477265950 | NECTIN1 | c.472C>A (p.Arg158=) n.446C>A | |
11 | g.119677817A>C | CA477265953 | NECTIN1 | c.471T>G (p.Leu157=) n.445T>G | |
11 | g.119677817A>G | CA477265955 | NECTIN1 | c.471T>C (p.Leu157=) n.445T>C | |
11 | g.119677817A>T | CA477265958 | NECTIN1 | c.471T>A (p.Leu157=) n.445T>A | |
11 | g.119677818A>C | CA383282223 | NECTIN1 | c.470T>G (p.Leu157Arg) n.444T>G | |
11 | g.119677818A>G | CA383282224 | NECTIN1 | c.470T>C (p.Leu157Pro) n.444T>C | |
11 | g.119677818A>T | CA383282225 | NECTIN1 | c.470T>A (p.Leu157His) n.444T>A | |
11 | g.119677819G>A | CA383282228 | NECTIN1 | c.469C>T (p.Leu157Phe) n.443C>T | gnomAD v4 |
11 | g.119677819G>C | CA383282226 | NECTIN1 | c.469C>G (p.Leu157Val) n.443C>G | |
11 | g.119677819G>T | CA383282227 | NECTIN1 | c.469C>A (p.Leu157Ile) n.443C>A | |
11 | g.119677820C>A | CA477265972 | NECTIN1 | c.468G>T (p.Val156=) n.442G>T | gnomAD v4 |
11 | g.119677820C>G | CA477265973 | NECTIN1 | c.468G>C (p.Val156=) n.442G>C | |
11 | g.119677820C>T | CA477265974 | NECTIN1 | c.468G>A (p.Val156=) n.442G>A | |
11 | g.119677821A>C | CA383282229 | NECTIN1 | c.467T>G (p.Val156Gly) n.441T>G | |
11 | g.119677821A>G | CA383282230 | NECTIN1 | c.467T>C (p.Val156Ala) n.441T>C | |
11 | g.119677821A>T | CA383282231 | NECTIN1 | c.467T>A (p.Val156Glu) n.441T>A | |
11 | g.119677822C>A | CA383282232 | NECTIN1 | c.466G>T (p.Val156Leu) n.440G>T | |
11 | g.119677822C>G | CA383282233 | NECTIN1 | c.466G>C (p.Val156Leu) n.440G>C | |
11 | g.119677822C>T | CA383282234 | NECTIN1 | c.466G>A (p.Val156Met) n.440G>A | |
11 | g.119677823T>A | CA6322074 | NECTIN1 | c.465A>T (p.Ala155=) n.439A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677823T>C | CA477266004 | NECTIN1 | c.465A>G (p.Ala155=) n.439A>G | |
11 | g.119677823T>G | CA477266005 | NECTIN1 | c.465A>C (p.Ala155=) n.439A>C | |
11 | g.119677823T= | CA2004079208 | NECTIN1 | c.465A= (p.Ala155=) n.439A= | |
11 | g.119677824G>A | CA229370451 | NECTIN1 | c.464C>T (p.Ala155Val) n.438C>T | dbSNP |
11 | g.119677824G>C | CA383282235 | NECTIN1 | c.464C>G (p.Ala155Gly) n.438C>G | |
11 | g.119677824G= | CA2004079217 | NECTIN1 | c.464C= (p.Ala155=) n.438C= | |
11 | g.119677824G>T | CA383282236 | NECTIN1 | c.464C>A (p.Ala155Glu) n.438C>A | COSMIC COSMIC COSMIC |
11 | g.119677825C>A | CA383282237 | NECTIN1 | c.463G>T (p.Ala155Ser) n.437G>T | |
11 | g.119677825C= | CA2004079222 | NECTIN1 | c.463G= (p.Ala155=) n.437G= | |
11 | g.119677825C>G | CA383282238 | NECTIN1 | c.463G>C (p.Ala155Pro) n.437G>C | dbSNP |
11 | g.119677825C>T | CA383282239 | NECTIN1 | c.463G>A (p.Ala155Thr) n.437G>A | |
11 | g.119677826C>A | CA383282241 | NECTIN1 | c.462G>T (p.Gln154His) n.436G>T | |
11 | g.119677826C>G | CA383282240 | NECTIN1 | c.462G>C (p.Gln154His) n.436G>C | gnomAD v4 |
11 | g.119677826C>T | CA477266025 | NECTIN1 | c.462G>A (p.Gln154=) n.436G>A | |
11 | g.119677827T>A | CA383282242 | NECTIN1 | c.461A>T (p.Gln154Leu) n.435A>T | |
11 | g.119677827T>C | CA383282243 | NECTIN1 | c.461A>G (p.Gln154Arg) n.435A>G | |
11 | g.119677827T>G | CA383282244 | NECTIN1 | c.461A>C (p.Gln154Pro) n.435A>C | |
11 | g.119677828G>A | CA383282245 | NECTIN1 | c.460C>T (p.Gln154Ter) n.434C>T | gnomAD v4 |
11 | g.119677828G>C | CA383282246 | NECTIN1 | c.460C>G (p.Gln154Glu) n.434C>G | |
11 | g.119677828G>T | CA383282247 | NECTIN1 | c.460C>A (p.Gln154Lys) n.434C>A | |
11 | g.119677829G>A | CA477266047 | NECTIN1 | c.459C>T (p.Thr153=) n.433C>T | |
11 | g.119677829G>C | CA6322075 | NECTIN1 | c.459C>G (p.Thr153=) n.433C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677829G= | CA2004079225 | NECTIN1 | c.459C= (p.Thr153=) n.433C= | |
11 | g.119677829G>T | CA477266052 | NECTIN1 | c.459C>A (p.Thr153=) n.433C>A | |
11 | g.119677830G>A | CA383282250 | NECTIN1 | c.458C>T (p.Thr153Ile) n.432C>T | gnomAD v4 COSMIC COSMIC COSMIC |
11 | g.119677830G>C | CA383282248 | NECTIN1 | c.458C>G (p.Thr153Ser) n.432C>G | |
11 | g.119677830G= | CA2004079230 | NECTIN1 | c.458C= (p.Thr153=) n.432C= | |
11 | g.119677830G>T | CA383282249 | NECTIN1 | c.458C>A (p.Thr153Asn) n.432C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.119677831T>A | CA383282251 | NECTIN1 | c.457A>T (p.Thr153Ser) n.431A>T | |
11 | g.119677831T>C | CA6322076 | NECTIN1 | c.457A>G (p.Thr153Ala) n.431A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677831T>G | CA383282252 | NECTIN1 | c.457A>C (p.Thr153Pro) n.431A>C | dbSNP |
11 | g.119677831T= | CA2004079233 | NECTIN1 | c.457A= (p.Thr153=) n.431A= | |
11 | g.119677832A= | CA2004079236 | NECTIN1 | c.456T= (p.Gly152=) n.430T= | |
11 | g.119677832A>C | CA477266062 | NECTIN1 | c.456T>G (p.Gly152=) n.430T>G | dbSNP |
11 | g.119677832A>G | CA477266065 | NECTIN1 | c.456T>C (p.Gly152=) n.430T>C | |
11 | g.119677832A>T | CA477266068 | NECTIN1 | c.456T>A (p.Gly152=) n.430T>A | |
11 | g.119677833C>A | CA383282253 | NECTIN1 | c.455G>T (p.Gly152Val) n.429G>T | |
11 | g.119677833C= | CA2004079240 | NECTIN1 | c.455G= (p.Gly152=) n.429G= | |
11 | g.119677833C>G | CA383282254 | NECTIN1 | c.455G>C (p.Gly152Ala) n.429G>C | |
11 | g.119677833C>T | CA383282255 | NECTIN1 | c.455G>A (p.Gly152Asp) n.429G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677834C>A | CA6322078 | NECTIN1 | c.454G>T (p.Gly152Cys) n.428G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677834C= | CA2004079247 | NECTIN1 | c.454G= (p.Gly152=) n.428G= | |
11 | g.119677834C>G | CA383282256 | NECTIN1 | c.454G>C (p.Gly152Arg) n.428G>C | dbSNP gnomAD v4 |
11 | g.119677834C>T | CA6322077 | NECTIN1 | c.454G>A (p.Gly152Ser) n.428G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677835C>A | CA383282257 | NECTIN1 | c.453G>T (p.Glu151Asp) n.427G>T | dbSNP gnomAD v4 |
11 | g.119677835C= | CA2004079251 | NECTIN1 | c.453G= (p.Glu151=) n.427G= | |
11 | g.119677835C>G | CA383282258 | NECTIN1 | c.453G>C (p.Glu151Asp) n.427G>C | gnomAD v4 |
11 | g.119677835C>T | CA477266081 | NECTIN1 | c.453G>A (p.Glu151=) n.427G>A | |
11 | g.119677836T>A | CA383282259 | NECTIN1 | c.452A>T (p.Glu151Val) n.426A>T | |
11 | g.119677836T>C | CA383282260 | NECTIN1 | c.452A>G (p.Glu151Gly) n.426A>G | |
11 | g.119677836T>G | CA383282261 | NECTIN1 | c.452A>C (p.Glu151Ala) n.426A>C | |
11 | g.119677837C>A | CA383282262 | NECTIN1 | c.451G>T (p.Glu151Ter) n.425G>T | COSMIC COSMIC COSMIC |
11 | g.119677837C>G | CA383282263 | NECTIN1 | c.451G>C (p.Glu151Gln) n.425G>C | |
11 | g.119677837C>T | CA383282264 | NECTIN1 | c.451G>A (p.Glu151Lys) n.425G>A | gnomAD v4 |
11 | g.119677838T>A | CA477266103 | NECTIN1 | c.450A>T (p.Ile150=) n.424A>T | |
11 | g.119677838T>C | CA383282265 | NECTIN1 | c.450A>G (p.Ile150Met) n.424A>G | |
11 | g.119677838T>G | CA477266108 | NECTIN1 | c.450A>C (p.Ile150=) n.424A>C | |
11 | g.119677839A>C | CA383282266 | NECTIN1 | c.449T>G (p.Ile150Arg) n.423T>G | |
11 | g.119677839A>G | CA383282267 | NECTIN1 | c.449T>C (p.Ile150Thr) n.423T>C | |
11 | g.119677839A>T | CA383282268 | NECTIN1 | c.449T>A (p.Ile150Lys) n.423T>A | |
11 | g.119677840T>A | CA383282269 | NECTIN1 | c.448A>T (p.Ile150Leu) n.422A>T | |
11 | g.119677840T>C | CA383282271 | NECTIN1 | c.448A>G (p.Ile150Val) n.422A>G | |
11 | g.119677840T>G | CA383282270 | NECTIN1 | c.448A>C (p.Ile150Leu) n.422A>C | |
11 | g.119677841C>A | CA383282272 | NECTIN1 | c.447G>T (p.Trp149Cys) n.421G>T | |
11 | g.119677841C>G | CA383282274 | NECTIN1 | c.447G>C (p.Trp149Cys) n.421G>C | |
11 | g.119677841C>T | CA383282273 | NECTIN1 | c.447G>A (p.Trp149Ter) n.421G>A | |
11 | g.119677842C>A | CA383282275 | NECTIN1 | c.446G>T (p.Trp149Leu) n.420G>T | |
11 | g.119677842C>G | CA383282276 | NECTIN1 | c.446G>C (p.Trp149Ser) n.420G>C | |
11 | g.119677842C>T | CA383282277 | NECTIN1 | c.446G>A (p.Trp149Ter) n.420G>A | |
11 | g.119677843A>C | CA383282278 | NECTIN1 | c.445T>G (p.Trp149Gly) n.419T>G | |
11 | g.119677843A>G | CA383282279 | NECTIN1 | c.445T>C (p.Trp149Arg) n.419T>C | |
11 | g.119677843A>T | CA383282280 | NECTIN1 | c.445T>A (p.Trp149Arg) n.419T>A | |
11 | g.119677844A= | CA2004079254 | NECTIN1 | c.444T= (p.Asn148=) n.418T= | |
11 | g.119677844A>C | CA383282281 | NECTIN1 | c.444T>G (p.Asn148Lys) n.418T>G | |
11 | g.119677844A>G | CA477266147 | NECTIN1 | c.444T>C (p.Asn148=) n.418T>C | ClinVar dbSNP gnomAD v4 |
11 | g.119677844A>T | CA383282282 | NECTIN1 | c.444T>A (p.Asn148Lys) n.418T>A | |
11 | g.119677845T>A | CA383282283 | NECTIN1 | c.443A>T (p.Asn148Ile) n.417A>T | |
11 | g.119677845T>C | CA383282284 | NECTIN1 | c.443A>G (p.Asn148Ser) n.417A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677845T>G | CA383282285 | NECTIN1 | c.443A>C (p.Asn148Thr) n.417A>C | |
11 | g.119677845T= | CA2004079258 | NECTIN1 | c.443A= (p.Asn148=) n.417A= | |
11 | g.119677846T>A | CA383282288 | NECTIN1 | c.442A>T (p.Asn148Tyr) n.416A>T | |
11 | g.119677846T>C | CA383282287 | NECTIN1 | c.442A>G (p.Asn148Asp) n.416A>G | |
11 | g.119677846T>G | CA383282286 | NECTIN1 | c.442A>C (p.Asn148His) n.416A>C | |
11 | g.119677847G>A | CA477266169 | NECTIN1 | c.441C>T (p.Thr147=) n.415C>T | |
11 | g.119677847G>C | CA477266171 | NECTIN1 | c.441C>G (p.Thr147=) n.415C>G | |
11 | g.119677847G>T | CA477266174 | NECTIN1 | c.441C>A (p.Thr147=) n.415C>A | |
11 | g.119677848G>A | CA383282289 | NECTIN1 | c.440C>T (p.Thr147Ile) n.414C>T | |
11 | g.119677848G>C | CA383282290 | NECTIN1 | c.440C>G (p.Thr147Ser) n.414C>G | gnomAD v4 |
11 | g.119677848G>T | CA383282291 | NECTIN1 | c.440C>A (p.Thr147Asn) n.414C>A | |
11 | g.119677849T>A | CA383282292 | NECTIN1 | c.439A>T (p.Thr147Ser) n.413A>T | |
11 | g.119677849T>C | CA383282293 | NECTIN1 | c.439A>G (p.Thr147Ala) n.413A>G | |
11 | g.119677849T>G | CA383282294 | NECTIN1 | c.439A>C (p.Thr147Pro) n.413A>C | |
11 | g.119677850G>A | CA477266182 | NECTIN1 | c.438C>T (p.Pro146=) n.412C>T | |
11 | g.119677850G>C | CA477266184 | NECTIN1 | c.438C>G (p.Pro146=) n.412C>G | |
11 | g.119677850G>T | CA477266188 | NECTIN1 | c.438C>A (p.Pro146=) n.412C>A | |
11 | g.119677851G>A | CA383282295 | NECTIN1 | c.437C>T (p.Pro146Leu) n.411C>T | |
11 | g.119677851G>C | CA383282296 | NECTIN1 | c.437C>G (p.Pro146Arg) n.411C>G | |
11 | g.119677851G= | CA2004079261 | NECTIN1 | c.437C= (p.Pro146=) n.411C= | |
11 | g.119677851G>T | CA383282297 | NECTIN1 | c.437C>A (p.Pro146His) n.411C>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.119677852G>A | CA383282298 | NECTIN1 | c.436C>T (p.Pro146Ser) n.410C>T | |
11 | g.119677852G>C | CA383282299 | NECTIN1 | c.436C>G (p.Pro146Ala) n.410C>G | |
11 | g.119677852G>T | CA383282300 | NECTIN1 | c.436C>A (p.Pro146Thr) n.410C>A | |
11 | g.119677853T>A | CA383282302 | NECTIN1 | c.435A>T (p.Lys145Asn) n.409A>T | gnomAD v4 |
11 | g.119677853T>C | CA477266210 | NECTIN1 | c.435A>G (p.Lys145=) n.409A>G | |
11 | g.119677853T>G | CA383282301 | NECTIN1 | c.435A>C (p.Lys145Asn) n.409A>C | dbSNP |
11 | g.119677853T= | CA2004079266 | NECTIN1 | c.435A= (p.Lys145=) n.409A= | |
11 | g.119677854T>A | CA383282303 | NECTIN1 | c.434A>T (p.Lys145Ile) n.408A>T | |
11 | g.119677854T>C | CA383282305 | NECTIN1 | c.434A>G (p.Lys145Arg) n.408A>G | |
11 | g.119677854T>G | CA383282304 | NECTIN1 | c.434A>C (p.Lys145Thr) n.408A>C |