| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.39665924G>A | CA399305096 | TCAP | c.319G>A (p.Glu107Lys) c.247G>A (p.Glu83Lys) | |
| 17 | g.39665924G>C | CA399305100 | TCAP | c.319G>C (p.Glu107Gln) c.247G>C (p.Glu83Gln) | |
| 17 | g.39665924G>T | CA399305103 | TCAP | c.319G>T (p.Glu107Ter) c.247G>T (p.Glu83Ter) | |
| 17 | g.39665925A>C | CA399305106 | TCAP | c.320A>C (p.Glu107Ala) c.248A>C (p.Glu83Ala) | |
| 17 | g.39665925A>G | CA399305108 | TCAP | c.320A>G (p.Glu107Gly) c.248A>G (p.Glu83Gly) | |
| 17 | g.39665925A>T | CA399305111 | TCAP | c.320A>T (p.Glu107Val) c.248A>T (p.Glu83Val) | |
| 17 | g.39665926G>A | CA499889181 | TCAP | c.321G>A (p.Glu107=) c.249G>A (p.Glu83=) | |
| 17 | g.39665926G>C | CA399305115 | TCAP | c.321G>C (p.Glu107Asp) c.249G>C (p.Glu83Asp) | |
| 17 | g.39665926G>T | CA399305116 | TCAP | c.321G>T (p.Glu107Asp) c.249G>T (p.Glu83Asp) | |
| 17 | g.39665927G>A | CA399305117 | TCAP | c.322G>A (p.Asp108Asn) c.250G>A (p.Asp84Asn) | gnomAD v4 |
| 17 | g.39665927G>C | CA399305118 | TCAP | c.322G>C (p.Asp108His) c.250G>C (p.Asp84His) | |
| 17 | g.39665927G>T | CA399305119 | TCAP | c.322G>T (p.Asp108Tyr) c.250G>T (p.Asp84Tyr) | |
| 17 | g.39665928A= | CA2259200820 | TCAP | c.323A= (p.Asp108=) c.251A= (p.Asp84=) | |
| 17 | g.39665928A>C | CA399305120 | TCAP | c.323A>C (p.Asp108Ala) c.251A>C (p.Asp84Ala) | |
| 17 | g.39665928A>G | CA290434154 | TCAP | c.323A>G (p.Asp108Gly) c.251A>G (p.Asp84Gly) | dbSNP gnomAD v4 |
| 17 | g.39665928A>T | CA399305128 | TCAP | c.323A>T (p.Asp108Val) c.251A>T (p.Asp84Val) | |
| 17 | g.39665929C>A | CA399305131 | TCAP | c.324C>A (p.Asp108Glu) c.252C>A (p.Asp84Glu) | |
| 17 | g.39665929C= | CA2259200821 | TCAP | c.324C= (p.Asp108=) c.252C= (p.Asp84=) | |
| 17 | g.39665929C>G | CA399305134 | TCAP | c.324C>G (p.Asp108Glu) c.252C>G (p.Asp84Glu) | dbSNP |
| 17 | g.39665929C>T | CA499889185 | TCAP | c.324C>T (p.Asp108=) c.252C>T (p.Asp84=) | gnomAD v4 |
| 17 | g.39665930A= | CA2259200822 | TCAP | c.325A= (p.Thr109=) c.253A= (p.Thr85=) | |
| 17 | g.39665930A>C | CA399305136 | TCAP | c.325A>C (p.Thr109Pro) c.253A>C (p.Thr85Pro) | dbSNP |
| 17 | g.39665930A>G | CA8532899 | TCAP | c.325A>G (p.Thr109Ala) c.253A>G (p.Thr85Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.39665930A>T | CA399305140 | TCAP | c.325A>T (p.Thr109Ser) c.253A>T (p.Thr85Ser) | |
| 17 | g.39665930_39665931delinsAC | CA2259200823 | TCAP | c.325_326delinsAC (p.Thr109=) c.253_254delinsAC (p.Thr85=) | |
| 17 | g.39665931C>A | CA399305147 | TCAP | c.326C>A (p.Thr109Asn) c.254C>A (p.Thr85Asn) | ClinVar |
| 17 | g.39665931C>G | CA399305146 | TCAP | c.326C>G (p.Thr109Ser) c.254C>G (p.Thr85Ser) | |
| 17 | g.39665931C>T | CA399305143 | TCAP | c.326C>T (p.Thr109Ile) c.254C>T (p.Thr85Ile) | COSMIC |
| 17 | g.39665935del | CA2259200824 | TCAP | c.330del (p.Ile111SerfsTer?) c.258del (p.Ile87SerfsTer?) | ClinVar dbSNP gnomAD v4 |
| 17 | g.39665932C>A | CA499889187 | TCAP | c.327C>A (p.Thr109=) c.255C>A (p.Thr85=) | dbSNP |
| 17 | g.39665932C>G | CA499889188 | TCAP | c.327C>G (p.Thr109=) c.255C>G (p.Thr85=) | |
| 17 | g.39665932C>T | CA499889189 | TCAP | c.327C>T (p.Thr109=) c.255C>T (p.Thr85=) | gnomAD v4 |
| 17 | g.39665933C>A | CA399305148 | TCAP | c.328C>A (p.Pro110Thr) c.256C>A (p.Pro86Thr) | dbSNP gnomAD v2 |
| 17 | g.39665933C= | CA2259200825 | TCAP | c.328C= (p.Pro110=) c.256C= (p.Pro86=) | |
| 17 | g.39665933C>G | CA399305149 | TCAP | c.328C>G (p.Pro110Ala) c.256C>G (p.Pro86Ala) | gnomAD v4 |
| 17 | g.39665933C>T | CA399305150 | TCAP | c.328C>T (p.Pro110Ser) c.256C>T (p.Pro86Ser) | |
| 17 | g.39665934C>A | CA399305154 | TCAP | c.329C>A (p.Pro110His) c.257C>A (p.Pro86His) | |
| 17 | g.39665934C= | CA2259200826 | TCAP | c.329C= (p.Pro110=) c.257C= (p.Pro86=) | |
| 17 | g.39665934C>G | CA399305156 | TCAP | c.329C>G (p.Pro110Arg) c.257C>G (p.Pro86Arg) | |
| 17 | g.39665934C>T | CA399305159 | TCAP | c.329C>T (p.Pro110Leu) c.257C>T (p.Pro86Leu) | dbSNP |
| 17 | g.39665935C>A | CA499889193 | TCAP | c.330C>A (p.Pro110=) c.258C>A (p.Pro86=) | ClinVar dbSNP |
| 17 | g.39665935C>G | CA499889194 | TCAP | c.330C>G (p.Pro110=) c.258C>G (p.Pro86=) | |
| 17 | g.39665935C>T | CA499889195 | TCAP | c.330C>T (p.Pro110=) c.258C>T (p.Pro86=) | |
| 17 | g.39665936A= | CA2259200827 | TCAP | c.331A= (p.Ile111=) c.259A= (p.Ile87=) | |
| 17 | g.39665936A>C | CA399305168 | TCAP | c.331A>C (p.Ile111Leu) c.259A>C (p.Ile87Leu) | ClinVar dbSNP |
| 17 | g.39665936A>G | CA399305163 | TCAP | c.331A>G (p.Ile111Val) c.259A>G (p.Ile87Val) | |
| 17 | g.39665936A>T | CA399305165 | TCAP | c.331A>T (p.Ile111Phe) c.259A>T (p.Ile87Phe) | |
| 17 | g.39665937T>A | CA399305174 | TCAP | c.332T>A (p.Ile111Asn) c.260T>A (p.Ile87Asn) | |
| 17 | g.39665937T>C | CA399305183 | TCAP | c.332T>C (p.Ile111Thr) c.260T>C (p.Ile87Thr) | gnomAD v4 |
| 17 | g.39665937T>G | CA399305185 | TCAP | c.332T>G (p.Ile111Ser) c.260T>G (p.Ile87Ser) | |
| 17 | g.39665937dup | CA8532900 | TCAP | c.332dup (p.Gln112ProfsTer24) c.260dup (p.Gln88ProfsTer24) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665938C>A | CA499889198 | TCAP | c.333C>A (p.Ile111=) c.261C>A (p.Ile87=) | |
| 17 | g.39665938C= | CA2259200828 | TCAP | c.333C= (p.Ile111=) c.261C= (p.Ile87=) | |
| 17 | g.39665938C>G | CA399305189 | TCAP | c.333C>G (p.Ile111Met) c.261C>G (p.Ile87Met) | |
| 17 | g.39665938C>T | CA290434156 | TCAP | c.333C>T (p.Ile111=) c.261C>T (p.Ile87=) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.39665939C>A | CA399305197 | TCAP | c.334C>A (p.Gln112Lys) c.262C>A (p.Gln88Lys) | |
| 17 | g.39665939C= | CA2259200829 | TCAP | c.334C= (p.Gln112=) c.262C= (p.Gln88=) | |
| 17 | g.39665939C>G | CA399305202 | TCAP | c.334C>G (p.Gln112Glu) c.262C>G (p.Gln88Glu) | |
| 17 | g.39665939C>T | CA308823 | TCAP | c.334C>T (p.Gln112Ter) c.262C>T (p.Gln88Ter) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.39665940A= | CA2259200830 | TCAP | c.335A= (p.Gln112=) c.263A= (p.Gln88=) | |
| 17 | g.39665940A>C | CA399305204 | TCAP | c.335A>C (p.Gln112Pro) c.263A>C (p.Gln88Pro) | |
| 17 | g.39665940A>G | CA399305206 | TCAP | c.335A>G (p.Gln112Arg) c.263A>G (p.Gln88Arg) | dbSNP gnomAD v4 |
| 17 | g.39665940A>T | CA399305209 | TCAP | c.335A>T (p.Gln112Leu) c.263A>T (p.Gln88Leu) | |
| 17 | g.39665941G>A | CA499889201 | TCAP | c.336G>A (p.Gln112=) c.264G>A (p.Gln88=) | |
| 17 | g.39665941G>C | CA399305211 | TCAP | c.336G>C (p.Gln112His) c.264G>C (p.Gln88His) | |
| 17 | g.39665941G>T | CA399305214 | TCAP | c.336G>T (p.Gln112His) c.264G>T (p.Gln88His) | |
| 17 | g.39665942C>A | CA399305217 | TCAP | c.337C>A (p.Leu113Ile) c.265C>A (p.Leu89Ile) | |
| 17 | g.39665942C= | CA2259200831 | TCAP | c.337C= (p.Leu113=) c.265C= (p.Leu89=) | |
| 17 | g.39665942C>G | CA399305220 | TCAP | c.337C>G (p.Leu113Val) c.265C>G (p.Leu89Val) | |
| 17 | g.39665942C>T | CA183562 | TCAP | c.337C>T (p.Leu113Phe) c.265C>T (p.Leu89Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665943T>A | CA399305224 | TCAP | c.338T>A (p.Leu113His) c.266T>A (p.Leu89His) | |
| 17 | g.39665943T>C | CA399305228 | TCAP | c.338T>C (p.Leu113Pro) c.266T>C (p.Leu89Pro) | |
| 17 | g.39665943T>G | CA399305235 | TCAP | c.338T>G (p.Leu113Arg) c.266T>G (p.Leu89Arg) | |
| 17 | g.39665944T>A | CA499889205 | TCAP | c.339T>A (p.Leu113=) c.267T>A (p.Leu89=) | |
| 17 | g.39665944T>C | CA499889207 | TCAP | c.339T>C (p.Leu113=) c.267T>C (p.Leu89=) | |
| 17 | g.39665944T>G | CA499889206 | TCAP | c.339T>G (p.Leu113=) c.267T>G (p.Leu89=) | dbSNP |
| 17 | g.39665944T= | CA2259200832 | TCAP | c.339T= (p.Leu113=) c.267T= (p.Leu89=) | |
| 17 | g.39665945C>A | CA399305243 | TCAP | c.340C>A (p.Gln114Lys) c.268C>A (p.Gln90Lys) | |
| 17 | g.39665945C>G | CA399305241 | TCAP | c.340C>G (p.Gln114Glu) c.268C>G (p.Gln90Glu) | |
| 17 | g.39665945C>T | CA399305238 | TCAP | c.340C>T (p.Gln114Ter) c.268C>T (p.Gln90Ter) | |
| 17 | g.39665946A= | CA2259200833 | TCAP | c.341A= (p.Gln114=) c.269A= (p.Gln90=) | |
| 17 | g.39665946A>C | CA399305247 | TCAP | c.341A>C (p.Gln114Pro) c.269A>C (p.Gln90Pro) | |
| 17 | g.39665946A>G | CA399305254 | TCAP | c.341A>G (p.Gln114Arg) c.269A>G (p.Gln90Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665946A>T | CA399305249 | TCAP | c.341A>T (p.Gln114Leu) c.269A>T (p.Gln90Leu) | |
| 17 | g.39665947G>A | CA499889211 | TCAP | c.342G>A (p.Gln114=) c.270G>A (p.Gln90=) | |
| 17 | g.39665947G>C | CA399305258 | TCAP | c.342G>C (p.Gln114His) c.270G>C (p.Gln90His) | |
| 17 | g.39665947G>T | CA399305260 | TCAP | c.342G>T (p.Gln114His) c.270G>T (p.Gln90His) | |
| 17 | g.39665948G>A | CA16615341 | TCAP | c.343G>A (p.Glu115Lys) c.271G>A (p.Glu91Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665948G>C | CA399305264 | TCAP | c.343G>C (p.Glu115Gln) c.271G>C (p.Glu91Gln) | |
| 17 | g.39665948G= | CA2259200834 | TCAP | c.343G= (p.Glu115=) c.271G= (p.Glu91=) | |
| 17 | g.39665948G>T | CA399305265 | TCAP | c.343G>T (p.Glu115Ter) c.271G>T (p.Glu91Ter) | |
| 17 | g.39665949A= | CA2259200835 | TCAP | c.344A= (p.Glu115=) c.272A= (p.Glu91=) | |
| 17 | g.39665949A>C | CA399305269 | TCAP | c.344A>C (p.Glu115Ala) c.272A>C (p.Glu91Ala) | |
| 17 | g.39665949A>G | CA399305278 | TCAP | c.344A>G (p.Glu115Gly) c.272A>G (p.Glu91Gly) | dbSNP |
| 17 | g.39665949A>T | CA399305281 | TCAP | c.344A>T (p.Glu115Val) c.272A>T (p.Glu91Val) | ClinVar dbSNP |
| 17 | g.39665950G>A | CA499889215 | TCAP | c.345G>A (p.Glu115=) c.273G>A (p.Glu91=) | |
| 17 | g.39665950G>C | CA399305283 | TCAP | c.345G>C (p.Glu115Asp) c.273G>C (p.Glu91Asp) | |
| 17 | g.39665950G>T | CA399305284 | TCAP | c.345G>T (p.Glu115Asp) c.273G>T (p.Glu91Asp) | dbSNP |
| 17 | g.39665951C>A | CA399305286 | TCAP | c.346C>A (p.Leu116Met) c.274C>A (p.Leu92Met) | dbSNP |
| 17 | g.39665951C= | CA2259200836 | TCAP | c.346C= (p.Leu116=) c.274C= (p.Leu92=) | |
| 17 | g.39665951C>G | CA399305285 | TCAP | c.346C>G (p.Leu116Val) c.274C>G (p.Leu92Val) | |
| 17 | g.39665951C>T | CA10577040 | TCAP | c.346C>T (p.Leu116=) c.274C>T (p.Leu92=) | ClinVar dbSNP COSMIC |
| 17 | g.39665952T>A | CA399305287 | TCAP | c.347T>A (p.Leu116Gln) c.275T>A (p.Leu92Gln) | |
| 17 | g.39665952T>C | CA399305288 | TCAP | c.347T>C (p.Leu116Pro) c.275T>C (p.Leu92Pro) | |
| 17 | g.39665952T>G | CA399305289 | TCAP | c.347T>G (p.Leu116Arg) c.275T>G (p.Leu92Arg) | |
| 17 | g.39665953G>A | CA499889217 | TCAP | c.348G>A (p.Leu116=) c.276G>A (p.Leu92=) | dbSNP |
| 17 | g.39665953G>C | CA499889218 | TCAP | c.348G>C (p.Leu116=) c.276G>C (p.Leu92=) | dbSNP |
| 17 | g.39665953G>T | CA499889219 | TCAP | c.348G>T (p.Leu116=) c.276G>T (p.Leu92=) | dbSNP gnomAD v4 |
| 17 | g.39665954C>A | CA399305290 | TCAP | c.349C>A (p.Leu117Met) c.277C>A (p.Leu93Met) | dbSNP |
| 17 | g.39665954C= | CA2259200837 | TCAP | c.349C= (p.Leu117=) c.277C= (p.Leu93=) | |
| 17 | g.39665954C>G | CA399305291 | TCAP | c.349C>G (p.Leu117Val) c.277C>G (p.Leu93Val) | |
| 17 | g.39665954C>T | CA10587267 | TCAP | c.349C>T (p.Leu117=) c.277C>T (p.Leu93=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665955T>A | CA399305292 | TCAP | c.350T>A (p.Leu117Gln) c.278T>A (p.Leu93Gln) | |
| 17 | g.39665955T>C | CA399305293 | TCAP | c.350T>C (p.Leu117Pro) c.278T>C (p.Leu93Pro) | |
| 17 | g.39665955T>G | CA399305294 | TCAP | c.350T>G (p.Leu117Arg) c.278T>G (p.Leu93Arg) | |
| 17 | g.39665956G>A | CA499889221 | TCAP | c.351G>A (p.Leu117=) c.279G>A (p.Leu93=) | dbSNP gnomAD v4 |
| 17 | g.39665956G>C | CA499889222 | TCAP | c.351G>C (p.Leu117=) c.279G>C (p.Leu93=) | |
| 17 | g.39665956G>T | CA499889223 | TCAP | c.351G>T (p.Leu117=) c.279G>T (p.Leu93=) | |
| 17 | g.39665957G>A | CA399305295 | TCAP | c.352G>A (p.Ala118Thr) c.280G>A (p.Ala94Thr) | dbSNP |
| 17 | g.39665957G>C | CA399305296 | TCAP | c.352G>C (p.Ala118Pro) c.280G>C (p.Ala94Pro) | dbSNP |
| 17 | g.39665957G>T | CA399305297 | TCAP | c.352G>T (p.Ala118Ser) c.280G>T (p.Ala94Ser) | |
| 17 | g.39665958C>A | CA399305298 | TCAP | c.353C>A (p.Ala118Glu) c.281C>A (p.Ala94Glu) | ClinVar dbSNP |
| 17 | g.39665958C= | CA2259200838 | TCAP | c.353C= (p.Ala118=) c.281C= (p.Ala94=) | |
| 17 | g.39665958C>G | CA399305299 | TCAP | c.353C>G (p.Ala118Gly) c.281C>G (p.Ala94Gly) | |
| 17 | g.39665958C>T | CA308826 | TCAP | c.353C>T (p.Ala118Val) c.281C>T (p.Ala94Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665959G>A | CA499889226 | TCAP | c.354G>A (p.Ala118=) c.282G>A (p.Ala94=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665959G>C | CA499889227 | TCAP | c.354G>C (p.Ala118=) c.282G>C (p.Ala94=) | ClinVar dbSNP |
| 17 | g.39665959G= | CA2259200839 | TCAP | c.354G= (p.Ala118=) c.282G= (p.Ala94=) | |
| 17 | g.39665959G>T | CA499889228 | TCAP | c.354G>T (p.Ala118=) c.282G>T (p.Ala94=) | ClinVar dbSNP COSMIC |
| 17 | g.39665960C>A | CA399305300 | TCAP | c.355C>A (p.Leu119Met) c.283C>A (p.Leu95Met) | |
| 17 | g.39665960C>G | CA399305301 | TCAP | c.355C>G (p.Leu119Val) c.283C>G (p.Leu95Val) | |
| 17 | g.39665960C>T | CA499889229 | TCAP | c.355C>T (p.Leu119=) c.283C>T (p.Leu95=) | dbSNP |
| 17 | g.39665961T>A | CA399305302 | TCAP | c.356T>A (p.Leu119Gln) c.284T>A (p.Leu95Gln) | |
| 17 | g.39665961T>C | CA399305304 | TCAP | c.356T>C (p.Leu119Pro) c.284T>C (p.Leu95Pro) | |
| 17 | g.39665961T>G | CA399305306 | TCAP | c.356T>G (p.Leu119Arg) c.284T>G (p.Leu95Arg) | dbSNP |
| 17 | g.39665962G>A | CA499889233 | TCAP | c.357G>A (p.Leu119=) c.285G>A (p.Leu95=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665962G>C | CA499889235 | TCAP | c.357G>C (p.Leu119=) c.285G>C (p.Leu95=) | |
| 17 | g.39665962G= | CA2259200840 | TCAP | c.357G= (p.Leu119=) c.285G= (p.Leu95=) | |
| 17 | g.39665962G>T | CA499889234 | TCAP | c.357G>T (p.Leu119=) c.285G>T (p.Leu95=) | |
| 17 | g.39665963G>A | CA399305308 | TCAP | c.358G>A (p.Glu120Lys) c.286G>A (p.Glu96Lys) | |
| 17 | g.39665963G>C | CA399305311 | TCAP | c.358G>C (p.Glu120Gln) c.286G>C (p.Glu96Gln) | dbSNP |
| 17 | g.39665963G>T | CA399305313 | TCAP | c.358G>T (p.Glu120Ter) c.286G>T (p.Glu96Ter) | dbSNP |
| 17 | g.39665965_39665966del | CA2580613273 | TCAP | c.360_361del (p.Glu120AspfsTer15) c.288_289del (p.Glu96AspfsTer15) | ClinVar |
| 17 | g.39665964A>C | CA399305315 | TCAP | c.359A>C (p.Glu120Ala) c.287A>C (p.Glu96Ala) | |
| 17 | g.39665964A>G | CA399305317 | TCAP | c.359A>G (p.Glu120Gly) c.287A>G (p.Glu96Gly) | dbSNP |
| 17 | g.39665964A>T | CA399305319 | TCAP | c.359A>T (p.Glu120Val) c.287A>T (p.Glu96Val) | dbSNP |
| 17 | g.39665965G>A | CA499889239 | TCAP | c.360G>A (p.Glu120=) c.288G>A (p.Glu96=) | dbSNP gnomAD v4 |
| 17 | g.39665965G>C | CA399305322 | TCAP | c.360G>C (p.Glu120Asp) c.288G>C (p.Glu96Asp) | |
| 17 | g.39665965G>T | CA399305324 | TCAP | c.360G>T (p.Glu120Asp) c.288G>T (p.Glu96Asp) | |
| 17 | g.39665965_39665966delinsGA | CA2259200841 | TCAP | c.360_361delinsGA (p.Glu120=) c.288_289delinsGA (p.Glu96=) | |
| 17 | g.39665966del | CA771858472 | TCAP | c.361del (p.Thr121GlnfsTer?) c.289del (p.Thr97GlnfsTer?) | dbSNP |
| 17 | g.39665966A>C | CA399305332 | TCAP | c.361A>C (p.Thr121Pro) c.289A>C (p.Thr97Pro) | |
| 17 | g.39665966A>G | CA399305328 | TCAP | c.361A>G (p.Thr121Ala) c.289A>G (p.Thr97Ala) | dbSNP |
| 17 | g.39665966A>T | CA399305326 | TCAP | c.361A>T (p.Thr121Ser) c.289A>T (p.Thr97Ser) | dbSNP |
| 17 | g.39665966_39665967delinsAC | CA2259200842 | TCAP | c.361_362delinsAC (p.Thr121=) c.289_290delinsAC (p.Thr97=) | |
| 17 | g.39665967del | CA919838668 | TCAP | c.362del (p.Thr121LysfsTer?) c.290del (p.Thr97LysfsTer?) | dbSNP gnomAD v4 |
| 17 | g.39665967C>A | CA399305334 | TCAP | c.362C>A (p.Thr121Lys) c.290C>A (p.Thr97Lys) | dbSNP |
| 17 | g.39665967C>G | CA399305335 | TCAP | c.362C>G (p.Thr121Arg) c.290C>G (p.Thr97Arg) | dbSNP |
| 17 | g.39665967C>T | CA399305336 | TCAP | c.362C>T (p.Thr121Ile) c.290C>T (p.Thr97Ile) | dbSNP |
| 17 | g.39665968A>C | CA499889243 | TCAP | c.363A>C (p.Thr121=) c.291A>C (p.Thr97=) | |
| 17 | g.39665968A>G | CA499889244 | TCAP | c.363A>G (p.Thr121=) c.291A>G (p.Thr97=) | dbSNP |
| 17 | g.39665968A>T | CA499889245 | TCAP | c.363A>T (p.Thr121=) c.291A>T (p.Thr97=) | dbSNP |
| 17 | g.39665969G>A | CA399305338 | TCAP | c.364G>A (p.Ala122Thr) c.292G>A (p.Ala98Thr) | dbSNP |
| 17 | g.39665969G>C | CA399305339 | TCAP | c.364G>C (p.Ala122Pro) c.292G>C (p.Ala98Pro) | |
| 17 | g.39665969G>T | CA399305341 | TCAP | c.364G>T (p.Ala122Ser) c.292G>T (p.Ala98Ser) | dbSNP |
| 17 | g.39665970C>A | CA399305343 | TCAP | c.365C>A (p.Ala122Asp) c.293C>A (p.Ala98Asp) | dbSNP |
| 17 | g.39665970C>G | CA399305345 | TCAP | c.365C>G (p.Ala122Gly) c.293C>G (p.Ala98Gly) | dbSNP |
| 17 | g.39665970C>T | CA399305347 | TCAP | c.365C>T (p.Ala122Val) c.293C>T (p.Ala98Val) | dbSNP gnomAD v4 |
| 17 | g.39665971C>A | CA499889248 | TCAP | c.366C>A (p.Ala122=) c.294C>A (p.Ala98=) | dbSNP gnomAD v4 |
| 17 | g.39665971C>G | CA499889249 | TCAP | c.366C>G (p.Ala122=) c.294C>G (p.Ala98=) | |
| 17 | g.39665971C>T | CA499889250 | TCAP | c.366C>T (p.Ala122=) c.294C>T (p.Ala98=) | gnomAD v4 |
| 17 | g.39665972C>A | CA399305349 | TCAP | c.367C>A (p.Leu123Met) c.295C>A (p.Leu99Met) | dbSNP |
| 17 | g.39665972C>G | CA399305351 | TCAP | c.367C>G (p.Leu123Val) c.295C>G (p.Leu99Val) | gnomAD v4 |
| 17 | g.39665972C>T | CA499889251 | TCAP | c.367C>T (p.Leu123=) c.295C>T (p.Leu99=) | dbSNP |
| 17 | g.39665972_39665982del | CA2637632987 | TCAP | c.367_377del (p.Leu123ValfsTer9) c.295_305del (p.Leu99ValfsTer9) | gnomAD v4 |
| 17 | g.39665973T>A | CA399305354 | TCAP | c.368T>A (p.Leu123Gln) c.296T>A (p.Leu99Gln) | |
| 17 | g.39665973T>C | CA399305357 | TCAP | c.368T>C (p.Leu123Pro) c.296T>C (p.Leu99Pro) | |
| 17 | g.39665973T>G | CA399305360 | TCAP | c.368T>G (p.Leu123Arg) c.296T>G (p.Leu99Arg) | ClinVar |
| 17 | g.39665974G>A | CA499889255 | TCAP | c.369G>A (p.Leu123=) c.297G>A (p.Leu99=) | dbSNP |
| 17 | g.39665974G>C | CA499889257 | TCAP | c.369G>C (p.Leu123=) c.297G>C (p.Leu99=) | |
| 17 | g.39665974G= | CA2259200843 | TCAP | c.369G= (p.Leu123=) c.297G= (p.Leu99=) | |
| 17 | g.39665974G>T | CA499889256 | TCAP | c.369G>T (p.Leu123=) c.297G>T (p.Leu99=) | dbSNP |
| 17 | g.39665976dup | CA2593710010 | TCAP | c.371dup (p.Gly125TrpfsTer11) c.299dup (p.Gly101TrpfsTer11) | gnomAD v3 gnomAD v4 |
| 17 | g.39665975G>A | CA399305365 | TCAP | c.370G>A (p.Gly124Ser) c.298G>A (p.Gly100Ser) | dbSNP |
| 17 | g.39665975G>C | CA399305368 | TCAP | c.370G>C (p.Gly124Arg) c.298G>C (p.Gly100Arg) | dbSNP |
| 17 | g.39665975G>T | CA399305363 | TCAP | c.370G>T (p.Gly124Cys) c.298G>T (p.Gly100Cys) | dbSNP |
| 17 | g.39665976G>A | CA399305372 | TCAP | c.371G>A (p.Gly124Asp) c.299G>A (p.Gly100Asp) | dbSNP gnomAD v2 |
| 17 | g.39665976G>C | CA399305377 | TCAP | c.371G>C (p.Gly124Ala) c.299G>C (p.Gly100Ala) | |
| 17 | g.39665976G= | CA2259200844 | TCAP | c.371G= (p.Gly124=) c.299G= (p.Gly100=) | |
| 17 | g.39665976G>T | CA399305374 | TCAP | c.371G>T (p.Gly124Val) c.299G>T (p.Gly100Val) | |
| 17 | g.39665977T>A | CA499889261 | TCAP | c.372T>A (p.Gly124=) c.300T>A (p.Gly100=) | dbSNP |
| 17 | g.39665977T>C | CA499889263 | TCAP | c.372T>C (p.Gly124=) c.300T>C (p.Gly100=) | dbSNP |
| 17 | g.39665977T>G | CA499889262 | TCAP | c.372T>G (p.Gly124=) c.300T>G (p.Gly100=) | |
| 17 | g.39665977T= | CA2259200845 | TCAP | c.372T= (p.Gly124=) c.300T= (p.Gly100=) | |
| 17 | g.39665978G>A | CA399305380 | TCAP | c.373G>A (p.Gly125Ser) c.301G>A (p.Gly101Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665978G>C | CA399305385 | TCAP | c.373G>C (p.Gly125Arg) c.301G>C (p.Gly101Arg) | |
| 17 | g.39665978G= | CA2259200847 | TCAP | c.373G= (p.Gly125=) c.301G= (p.Gly101=) | |
| 17 | g.39665978G>T | CA399305383 | TCAP | c.373G>T (p.Gly125Cys) c.301G>T (p.Gly101Cys) | |
| 17 | g.39665978_39665993delinsGGCCAGTGTGTGGACC | CA2259200846 | TCAP | c.373_388delinsGGCCAGTGTGTGGACC (p.Gly125=) c.301_316delinsGGCCAGTGTGTGGACC (p.Gly101=) | |
| 17 | g.39665979G>A | CA399305389 | TCAP | c.374G>A (p.Gly125Asp) c.302G>A (p.Gly101Asp) | dbSNP gnomAD v4 |
| 17 | g.39665979G>C | CA399305394 | TCAP | c.374G>C (p.Gly125Ala) c.302G>C (p.Gly101Ala) | |
| 17 | g.39665979G>T | CA399305396 | TCAP | c.374G>T (p.Gly125Val) c.302G>T (p.Gly101Val) | |
| 17 | g.39665984_39665998del | CA8532901 | TCAP | c.379_393del (p.Cys127_Gln131del) c.307_321del (p.Cys103_Gln107del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.39665980C>A | CA499889264 | TCAP | c.375C>A (p.Gly125=) c.303C>A (p.Gly101=) | dbSNP |
| 17 | g.39665980C= | CA2259200848 | TCAP | c.375C= (p.Gly125=) c.303C= (p.Gly101=) | |
| 17 | g.39665980C>G | CA499889265 | TCAP | c.375C>G (p.Gly125=) c.303C>G (p.Gly101=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665980C>T | CA499889266 | TCAP | c.375C>T (p.Gly125=) c.303C>T (p.Gly101=) | dbSNP |
| 17 | g.39665981C>A | CA399305405 | TCAP | c.376C>A (p.Gln126Lys) c.304C>A (p.Gln102Lys) | dbSNP |
| 17 | g.39665981C>G | CA399305400 | TCAP | c.376C>G (p.Gln126Glu) c.304C>G (p.Gln102Glu) | dbSNP |
| 17 | g.39665981C>T | CA399305403 | TCAP | c.376C>T (p.Gln126Ter) c.304C>T (p.Gln102Ter) | dbSNP COSMIC |
| 17 | g.39665982A= | CA2259200849 | TCAP | c.377A= (p.Gln126=) c.305A= (p.Gln102=) | |
| 17 | g.39665982A>C | CA399305409 | TCAP | c.377A>C (p.Gln126Pro) c.305A>C (p.Gln102Pro) | |
| 17 | g.39665982A>G | CA8532902 | TCAP | c.377A>G (p.Gln126Arg) c.305A>G (p.Gln102Arg) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 17 | g.39665982A>T | CA399305414 | TCAP | c.377A>T (p.Gln126Leu) c.305A>T (p.Gln102Leu) | |
| 17 | g.39665983G>A | CA499889269 | TCAP | c.378G>A (p.Gln126=) c.306G>A (p.Gln102=) | dbSNP |
| 17 | g.39665983G>C | CA8532903 | TCAP | c.378G>C (p.Gln126His) c.306G>C (p.Gln102His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665983G= | CA2259200850 | TCAP | c.378G= (p.Gln126=) c.306G= (p.Gln102=) | |
| 17 | g.39665983G>T | CA399305418 | TCAP | c.378G>T (p.Gln126His) c.306G>T (p.Gln102His) | |
| 17 | g.39665984T>A | CA399305427 | TCAP | c.379T>A (p.Cys127Ser) c.307T>A (p.Cys103Ser) | |
| 17 | g.39665984T>C | CA399305422 | TCAP | c.379T>C (p.Cys127Arg) c.307T>C (p.Cys103Arg) | |
| 17 | g.39665984T>G | CA399305423 | TCAP | c.379T>G (p.Cys127Gly) c.307T>G (p.Cys103Gly) | dbSNP |
| 17 | g.39665985G>A | CA399305430 | TCAP | c.380G>A (p.Cys127Tyr) c.308G>A (p.Cys103Tyr) | ClinVar dbSNP |
| 17 | g.39665985G>C | CA399305434 | TCAP | c.380G>C (p.Cys127Ser) c.308G>C (p.Cys103Ser) | |
| 17 | g.39665985G= | CA2259200851 | TCAP | c.380G= (p.Cys127=) c.308G= (p.Cys103=) | |
| 17 | g.39665985G>T | CA399305437 | TCAP | c.380G>T (p.Cys127Phe) c.308G>T (p.Cys103Phe) | dbSNP |
| 17 | g.39665986T>A | CA399305439 | TCAP | c.381T>A (p.Cys127Ter) c.309T>A (p.Cys103Ter) | |
| 17 | g.39665986T>C | CA499889273 | TCAP | c.381T>C (p.Cys127=) c.309T>C (p.Cys103=) | ClinVar dbSNP |
| 17 | g.39665986T>G | CA399305442 | TCAP | c.381T>G (p.Cys127Trp) c.309T>G (p.Cys103Trp) | |
| 17 | g.39665986T= | CA2259200852 | TCAP | c.381T= (p.Cys127=) c.309T= (p.Cys103=) | |
| 17 | g.39665987G>A | CA399305445 | TCAP | c.382G>A (p.Val128Met) c.310G>A (p.Val104Met) | gnomAD v4 |
| 17 | g.39665987G>C | CA399305451 | TCAP | c.382G>C (p.Val128Leu) c.310G>C (p.Val104Leu) | ClinVar |
| 17 | g.39665987G>T | CA399305446 | TCAP | c.382G>T (p.Val128Leu) c.310G>T (p.Val104Leu) | |
| 17 | g.39665988T>A | CA399305454 | TCAP | c.383T>A (p.Val128Glu) c.311T>A (p.Val104Glu) | |
| 17 | g.39665988T>C | CA399305456 | TCAP | c.383T>C (p.Val128Ala) c.311T>C (p.Val104Ala) | |
| 17 | g.39665988T>G | CA399305460 | TCAP | c.383T>G (p.Val128Gly) c.311T>G (p.Val104Gly) | |
| 17 | g.39665989G>A | CA499889277 | TCAP | c.384G>A (p.Val128=) c.312G>A (p.Val104=) | dbSNP |
| 17 | g.39665989G>C | CA499889278 | TCAP | c.384G>C (p.Val128=) c.312G>C (p.Val104=) | |
| 17 | g.39665989G>T | CA499889279 | TCAP | c.384G>T (p.Val128=) c.312G>T (p.Val104=) | |
| 17 | g.39665990G>A | CA399305462 | TCAP | c.385G>A (p.Asp129Asn) c.313G>A (p.Asp105Asn) | |
| 17 | g.39665990G>C | CA399305464 | TCAP | c.385G>C (p.Asp129His) c.313G>C (p.Asp105His) | |
| 17 | g.39665990G>T | CA399305466 | TCAP | c.385G>T (p.Asp129Tyr) c.313G>T (p.Asp105Tyr) | dbSNP gnomAD v4 |
| 17 | g.39665991A= | CA2259200853 | TCAP | c.386A= (p.Asp129=) c.314A= (p.Asp105=) | |
| 17 | g.39665991A>C | CA399305471 | TCAP | c.386A>C (p.Asp129Ala) c.314A>C (p.Asp105Ala) | ClinVar dbSNP gnomAD v4 |
| 17 | g.39665991A>G | CA399305473 | TCAP | c.386A>G (p.Asp129Gly) c.314A>G (p.Asp105Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665991A>T | CA399305475 | TCAP | c.386A>T (p.Asp129Val) c.314A>T (p.Asp105Val) | dbSNP |
| 17 | g.39665992C>A | CA399305479 | TCAP | c.387C>A (p.Asp129Glu) c.315C>A (p.Asp105Glu) | dbSNP |
| 17 | g.39665992C= | CA2259200854 | TCAP | c.387C= (p.Asp129=) c.315C= (p.Asp105=) | |
| 17 | g.39665992C>G | CA8532904 | TCAP | c.387C>G (p.Asp129Glu) c.315C>G (p.Asp105Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.39665992C>T | CA499889280 | TCAP | c.387C>T (p.Asp129=) c.315C>T (p.Asp105=) | ClinVar dbSNP |
| 17 | g.39665993C>A | CA184980 | TCAP | c.388C>A (p.Arg130Ser) c.316C>A (p.Arg106Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665993C= | CA2259200855 | TCAP | c.388C= (p.Arg130=) c.316C= (p.Arg106=) | |
| 17 | g.39665993C>G | CA399305487 | TCAP | c.388C>G (p.Arg130Gly) c.316C>G (p.Arg106Gly) | dbSNP |
| 17 | g.39665993C>T | CA134923 | TCAP | c.388C>T (p.Arg130Cys) c.316C>T (p.Arg106Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665994G>A | CA241516 | TCAP | c.389G>A (p.Arg130His) c.317G>A (p.Arg106His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39665994G>C | CA399305492 | TCAP | c.389G>C (p.Arg130Pro) c.317G>C (p.Arg106Pro) | ClinVar dbSNP gnomAD v4 |
| 17 | g.39665994G= | CA2259200856 | TCAP | c.389G= (p.Arg130=) c.317G= (p.Arg106=) | |
| 17 | g.39665994G>T | CA399305494 | TCAP | c.389G>T (p.Arg130Leu) c.317G>T (p.Arg106Leu) | dbSNP gnomAD v4 COSMIC |
| 17 | g.39665995C>A | CA499889286 | TCAP | c.390C>A (p.Arg130=) c.318C>A (p.Arg106=) | |
| 17 | g.39665995C= | CA2259200857 | TCAP | c.390C= (p.Arg130=) c.318C= (p.Arg106=) | |
| 17 | g.39665995C>G | CA499889284 | TCAP | c.390C>G (p.Arg130=) c.318C>G (p.Arg106=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.39665995C>T | CA499889285 | TCAP | c.390C>T (p.Arg130=) c.318C>T (p.Arg106=) | |
| 17 | g.39665996C>A | CA399305497 | TCAP | c.391C>A (p.Gln131Lys) c.319C>A (p.Gln107Lys) | |
| 17 | g.39665996C>G | CA399305499 | TCAP | c.391C>G (p.Gln131Glu) c.319C>G (p.Gln107Glu) | |
| 17 | g.39665996C>T | CA399305501 | TCAP | c.391C>T (p.Gln131Ter) c.319C>T (p.Gln107Ter) | dbSNP |
| 17 | g.39665997A>C | CA399305505 | TCAP | c.392A>C (p.Gln131Pro) c.320A>C (p.Gln107Pro) | |
| 17 | g.39665997A>G | CA399305508 | TCAP | c.392A>G (p.Gln131Arg) c.320A>G (p.Gln107Arg) | dbSNP |
| 17 | g.39665997A>T | CA399305511 | TCAP | c.392A>T (p.Gln131Leu) c.320A>T (p.Gln107Leu) | |
| 17 | g.39665998G>A | CA499889288 | TCAP | c.393G>A (p.Gln131=) c.321G>A (p.Gln107=) | dbSNP |
| 17 | g.39665998G>C | CA399305513 | TCAP | c.393G>C (p.Gln131His) c.321G>C (p.Gln107His) | dbSNP |
| 17 | g.39665998G>T | CA399305515 | TCAP | c.393G>T (p.Gln131His) c.321G>T (p.Gln107His) | dbSNP |
| 17 | g.39665999G>A | CA8532905 | TCAP | c.394G>A (p.Glu132Lys) c.322G>A (p.Glu108Lys) | ClinVar dbSNP ExAC gnomAD v2 |
| 17 | g.39665999G>C | CA399305521 | TCAP | c.394G>C (p.Glu132Gln) c.322G>C (p.Glu108Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39665999G= | CA2259200858 | TCAP | c.394G= (p.Glu132=) c.322G= (p.Glu108=) | |
| 17 | g.39665999G>T | CA399305519 | TCAP | c.394G>T (p.Glu132Ter) c.322G>T (p.Glu108Ter) | dbSNP gnomAD v4 |
| 17 | g.39666000del | CA2637633062 | TCAP | c.395del (p.Glu132GlyfsTer?) c.323del (p.Glu108GlyfsTer?) | gnomAD v4 |
| 17 | g.39666000A= | CA2259200859 | TCAP | c.395A= (p.Glu132=) c.323A= (p.Glu108=) | |
| 17 | g.39666000A>C | CA399305526 | TCAP | c.395A>C (p.Glu132Ala) c.323A>C (p.Glu108Ala) | dbSNP |
| 17 | g.39666000A>G | CA399305529 | TCAP | c.395A>G (p.Glu132Gly) c.323A>G (p.Glu108Gly) | dbSNP |
| 17 | g.39666000A>T | CA399305530 | TCAP | c.395A>T (p.Glu132Val) c.323A>T (p.Glu108Val) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.39666001G>A | CA499889290 | TCAP | c.396G>A (p.Glu132=) c.324G>A (p.Glu108=) | ClinVar dbSNP gnomAD v4 |
| 17 | g.39666001G>C | CA399305534 | TCAP | c.396G>C (p.Glu132Asp) c.324G>C (p.Glu108Asp) | dbSNP |
| 17 | g.39666001G= | CA2259200860 | TCAP | c.396G= (p.Glu132=) c.324G= (p.Glu108=) | |
| 17 | g.39666001G>T | CA399305537 | TCAP | c.396G>T (p.Glu132Asp) c.324G>T (p.Glu108Asp) | dbSNP gnomAD v4 |
| 17 | g.39666002G>A | CA399305539 | TCAP | c.397G>A (p.Val133Met) c.325G>A (p.Val109Met) | ClinVar dbSNP |
| 17 | g.39666002G>C | CA399305542 | TCAP | c.397G>C (p.Val133Leu) c.325G>C (p.Val109Leu) | dbSNP |
| 17 | g.39666002G>T | CA399305544 | TCAP | c.397G>T (p.Val133Leu) c.325G>T (p.Val109Leu) | |
| 17 | g.39666002_39666017del | CA2637633069 | TCAP | c.397_412del (p.Val133SerfsTer?) c.325_340del (p.Val109SerfsTer?) | gnomAD v4 |
| 17 | g.39666003T>A | CA399305547 | TCAP | c.398T>A (p.Val133Glu) c.326T>A (p.Val109Glu) | dbSNP |
| 17 | g.39666003T>C | CA399305549 | TCAP | c.398T>C (p.Val133Ala) c.326T>C (p.Val109Ala) | |
| 17 | g.39666003T>G | CA399305552 | TCAP | c.398T>G (p.Val133Gly) c.326T>G (p.Val109Gly) | dbSNP |
| 17 | g.39666004G>A | CA499889292 | TCAP | c.399G>A (p.Val133=) c.327G>A (p.Val109=) | |
| 17 | g.39666004G>C | CA499889294 | TCAP | c.399G>C (p.Val133=) c.327G>C (p.Val109=) | |
| 17 | g.39666004G>T | CA499889293 | TCAP | c.399G>T (p.Val133=) c.327G>T (p.Val109=) | dbSNP |
| 17 | g.39666005G>A | CA399305561 | TCAP | c.400G>A (p.Ala134Thr) c.328G>A (p.Ala110Thr) | dbSNP gnomAD v2 |
| 17 | g.39666005G>C | CA399305558 | TCAP | c.400G>C (p.Ala134Pro) c.328G>C (p.Ala110Pro) | |
| 17 | g.39666005G= | CA2259200861 | TCAP | c.400G= (p.Ala134=) c.328G= (p.Ala110=) | |
| 17 | g.39666005G>T | CA399305554 | TCAP | c.400G>T (p.Ala134Ser) c.328G>T (p.Ala110Ser) | dbSNP gnomAD v4 |
| 17 | g.39666006C>A | CA237513 | TCAP | c.401C>A (p.Ala134Asp) c.329C>A (p.Ala110Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39666006C= | CA2259200862 | TCAP | c.401C= (p.Ala134=) c.329C= (p.Ala110=) | |
| 17 | g.39666006C>G | CA399305563 | TCAP | c.401C>G (p.Ala134Gly) c.329C>G (p.Ala110Gly) | dbSNP |
| 17 | g.39666006C>T | CA399305562 | TCAP | c.401C>T (p.Ala134Val) c.329C>T (p.Ala110Val) | dbSNP |
| 17 | g.39666007del | CA2637633082 | TCAP | c.402del (p.Glu135ArgfsTer?) c.330del (p.Glu111ArgfsTer?) | ClinVar gnomAD v4 |
| 17 | g.39666007T>A | CA499889296 | TCAP | c.402T>A (p.Ala134=) c.330T>A (p.Ala110=) | dbSNP |
| 17 | g.39666007T>C | CA499889297 | TCAP | c.402T>C (p.Ala134=) c.330T>C (p.Ala110=) | dbSNP |
| 17 | g.39666007T>G | CA8532906 | TCAP | c.402T>G (p.Ala134=) c.330T>G (p.Ala110=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.39666007T= | CA2259200863 | TCAP | c.402T= (p.Ala134=) c.330T= (p.Ala110=) | |
| 17 | g.39666008G>A | CA399305564 | TCAP | c.403G>A (p.Glu135Lys) c.331G>A (p.Glu111Lys) | dbSNP gnomAD v4 |
| 17 | g.39666008G>C | CA399305566 | TCAP | c.403G>C (p.Glu135Gln) c.331G>C (p.Glu111Gln) | dbSNP |
| 17 | g.39666008G>T | CA399305569 | TCAP | c.403G>T (p.Glu135Ter) c.331G>T (p.Glu111Ter) | gnomAD v4 |
| 17 | g.39666009A>C | CA399305571 | TCAP | c.404A>C (p.Glu135Ala) c.332A>C (p.Glu111Ala) | |
| 17 | g.39666009A>G | CA399305573 | TCAP | c.404A>G (p.Glu135Gly) c.332A>G (p.Glu111Gly) | dbSNP |
| 17 | g.39666009A>T | CA399305576 | TCAP | c.404A>T (p.Glu135Val) c.332A>T (p.Glu111Val) | dbSNP |
| 17 | g.39666010G>A | CA499889299 | TCAP | c.405G>A (p.Glu135=) c.333G>A (p.Glu111=) | gnomAD v4 |
| 17 | g.39666010G>C | CA399305578 | TCAP | c.405G>C (p.Glu135Asp) c.333G>C (p.Glu111Asp) | dbSNP |
| 17 | g.39666010G>T | CA399305581 | TCAP | c.405G>T (p.Glu135Asp) c.333G>T (p.Glu111Asp) | dbSNP |
| 17 | g.39666011A>C | CA399305584 | TCAP | c.406A>C (p.Ile136Leu) c.334A>C (p.Ile112Leu) | ClinVar dbSNP |
| 17 | g.39666011A>G | CA399305586 | TCAP | c.406A>G (p.Ile136Val) c.334A>G (p.Ile112Val) | |
| 17 | g.39666011A>T | CA399305588 | TCAP | c.406A>T (p.Ile136Phe) c.334A>T (p.Ile112Phe) | |
| 17 | g.39666012T>A | CA399305742 | TCAP | c.407T>A (p.Ile136Asn) c.335T>A (p.Ile112Asn) | ClinVar dbSNP |
| 17 | g.39666012T>C | CA399305737 | TCAP | c.407T>C (p.Ile136Thr) c.335T>C (p.Ile112Thr) | |
| 17 | g.39666012T>G | CA399305740 | TCAP | c.407T>G (p.Ile136Ser) c.335T>G (p.Ile112Ser) | ClinVar dbSNP |
| 17 | g.39666013del | CA2637633102 | TCAP | c.408del (p.Thr137GlnfsTer?) c.336del (p.Thr113GlnfsTer?) | gnomAD v4 |
| 17 | g.39666013C>A | CA499670482 | TCAP | c.408C>A (p.Ile136=) c.336C>A (p.Ile112=) | dbSNP |
| 17 | g.39666013C>G | CA399305744 | TCAP | c.408C>G (p.Ile136Met) c.336C>G (p.Ile112Met) | dbSNP |
| 17 | g.39666013C>T | CA499670483 | TCAP | c.408C>T (p.Ile136=) c.336C>T (p.Ile112=) | dbSNP |
| 17 | g.39666013_39666015delinsA | CA2580093662 | TCAP | c.408_410delinsA (p.Thr137LysfsTer?) c.336_338delinsA (p.Thr113LysfsTer?) | ClinVar |
| 17 | g.39666015_39666016del | CA2576253852 | TCAP | c.410_411del (p.Thr137LysfsTer?) c.338_339del (p.Thr113LysfsTer?) | ClinVar |
| 17 | g.39666014A>C | CA399305749 | TCAP | c.409A>C (p.Thr137Pro) c.337A>C (p.Thr113Pro) | gnomAD v4 |
| 17 | g.39666014A>G | CA399305751 | TCAP | c.409A>G (p.Thr137Ala) c.337A>G (p.Thr113Ala) | |
| 17 | g.39666014A>T | CA399305753 | TCAP | c.409A>T (p.Thr137Ser) c.337A>T (p.Thr113Ser) | dbSNP |
| 17 | g.39666015del | CA2637633110 | TCAP | c.410del (p.Thr137LysfsTer?) c.338del (p.Thr113LysfsTer?) | gnomAD v4 |
| 17 | g.39666015C>A | CA8532907 | TCAP | c.410C>A (p.Thr137Lys) c.338C>A (p.Thr113Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.39666015C= | CA2259200864 | TCAP | c.410C= (p.Thr137=) c.338C= (p.Thr113=) | |
| 17 | g.39666015C>G | CA399305758 | TCAP | c.410C>G (p.Thr137Arg) c.338C>G (p.Thr113Arg) | dbSNP |
| 17 | g.39666015C>T | CA274680 | TCAP | c.410C>T (p.Thr137Ile) c.338C>T (p.Thr113Ile) | ClinVar dbSNP |
| 17 | g.39666016A= | CA2259200865 | TCAP | c.411A= (p.Thr137=) c.339A= (p.Thr113=) | |
| 17 | g.39666016A>C | CA499670486 | TCAP | c.411A>C (p.Thr137=) c.339A>C (p.Thr113=) | dbSNP |
| 17 | g.39666016A>G | CA499670487 | TCAP | c.411A>G (p.Thr137=) c.339A>G (p.Thr113=) | COSMIC |
| 17 | g.39666016A>T | CA499670488 | TCAP | c.411A>T (p.Thr137=) c.339A>T (p.Thr113=) | |
| 17 | g.39666017A>C | CA399305763 | TCAP | c.412A>C (p.Lys138Gln) c.340A>C (p.Lys114Gln) | |
| 17 | g.39666017A>G | CA399305765 | TCAP | c.412A>G (p.Lys138Glu) c.340A>G (p.Lys114Glu) | dbSNP gnomAD v4 |
| 17 | g.39666017A>T | CA399305768 | TCAP | c.412A>T (p.Lys138Ter) c.340A>T (p.Lys114Ter) | dbSNP |
| 17 | g.39666018A>C | CA399305776 | TCAP | c.413A>C (p.Lys138Thr) c.341A>C (p.Lys114Thr) | |
| 17 | g.39666018A>G | CA399305774 | TCAP | c.413A>G (p.Lys138Arg) c.341A>G (p.Lys114Arg) | dbSNP |
| 17 | g.39666018A>T | CA399305772 | TCAP | c.413A>T (p.Lys138Met) c.341A>T (p.Lys114Met) | dbSNP |
| 17 | g.39666019G>A | CA499670489 | TCAP | c.414G>A (p.Lys138=) c.342G>A (p.Lys114=) | dbSNP |
| 17 | g.39666019G>C | CA399305779 | TCAP | c.414G>C (p.Lys138Asn) c.342G>C (p.Lys114Asn) | dbSNP |
| 17 | g.39666019G>T | CA399305781 | TCAP | c.414G>T (p.Lys138Asn) c.342G>T (p.Lys114Asn) | gnomAD v4 |
| 17 | g.39666020C>A | CA399305785 | TCAP | c.415C>A (p.Gln139Lys) c.343C>A (p.Gln115Lys) | |
| 17 | g.39666020C>G | CA399305787 | TCAP | c.415C>G (p.Gln139Glu) c.343C>G (p.Gln115Glu) | dbSNP |
| 17 | g.39666020C>T | CA399305789 | TCAP | c.415C>T (p.Gln139Ter) c.343C>T (p.Gln115Ter) | ClinVar dbSNP |
| 17 | g.39666021A>C | CA399305792 | TCAP | c.416A>C (p.Gln139Pro) c.344A>C (p.Gln115Pro) | |
| 17 | g.39666021A>G | CA399305795 | TCAP | c.416A>G (p.Gln139Arg) c.344A>G (p.Gln115Arg) | |
| 17 | g.39666021A>T | CA399305797 | TCAP | c.416A>T (p.Gln139Leu) c.344A>T (p.Gln115Leu) | dbSNP |
| 17 | g.39666022G>A | CA499670493 | TCAP | c.417G>A (p.Gln139=) c.345G>A (p.Gln115=) | dbSNP |
| 17 | g.39666022G>C | CA399305800 | TCAP | c.417G>C (p.Gln139His) c.345G>C (p.Gln115His) | dbSNP |
| 17 | g.39666022G>T | CA399305802 | TCAP | c.417G>T (p.Gln139His) c.345G>T (p.Gln115His) | |
| 17 | g.39666023C>A | CA399305805 | TCAP | c.418C>A (p.Leu140Met) c.346C>A (p.Leu116Met) | gnomAD v4 |
| 17 | g.39666023C>G | CA399305806 | TCAP | c.418C>G (p.Leu140Val) c.346C>G (p.Leu116Val) | |
| 17 | g.39666023C>T | CA499670494 | TCAP | c.418C>T (p.Leu140=) c.346C>T (p.Leu116=) | dbSNP |
| 17 | g.39666024T>A | CA399305814 | TCAP | c.419T>A (p.Leu140Gln) c.347T>A (p.Leu116Gln) | dbSNP |
| 17 | g.39666024T>C | CA399305812 | TCAP | c.419T>C (p.Leu140Pro) c.347T>C (p.Leu116Pro) | dbSNP |
| 17 | g.39666024T>G | CA399305810 | TCAP | c.419T>G (p.Leu140Arg) c.347T>G (p.Leu116Arg) | dbSNP |