Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49451683_49451706del | CA913110642 | MMUT | c.1092_1115del (p.Tyr364Ter) | |
6 | g.49451683_49451706delinsATTGCAGTACGGACAATATTATTG | CA1627389369 | MMUT | c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT (p.Tyr364=) | |
6 | g.49451685_49451707del | CA567155986 | MMUT | c.1092_1114del (p.Asn365ArgfsTer19) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451693G>A | CA347895 | MMUT | c.1105C>T (p.Arg369Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451693G>C | CA364399134 | MMUT | c.1105C>G (p.Arg369Gly) | |
6 | g.49451693G= | CA1627389374 | MMUT | c.1105C= (p.Arg369=) | |
6 | g.49451693G>T | CA364399136 | MMUT | c.1105C>A (p.Arg369Ser) | |
6 | g.49451694G>A | CA450606661 | MMUT | c.1104C>T (p.Val368=) | |
6 | g.49451694G>C | CA450606662 | MMUT | c.1104C>G (p.Val368=) | |
6 | g.49451694G>T | CA450606663 | MMUT | c.1104C>A (p.Val368=) | |
6 | g.49451695A>C | CA364399139 | MMUT | c.1103T>G (p.Val368Gly) | |
6 | g.49451695A>G | CA364399140 | MMUT | c.1103T>C (p.Val368Ala) | gnomAD v4 |
6 | g.49451695A>T | CA364399141 | MMUT | c.1103T>A (p.Val368Asp) | |
6 | g.49451695_49451696delinsAC | CA1627389375 | MMUT | c.1102_1103delinsGT (p.Val368=) | |
6 | g.49451696del | CA1139659594 | MMUT | c.1102del (p.Val368SerfsTer5) | ClinVar dbSNP |
6 | g.49451696C>A | CA364399142 | MMUT | c.1102G>T (p.Val368Phe) | |
6 | g.49451696C= | CA1627389376 | MMUT | c.1102G= (p.Val368=) | |
6 | g.49451696C>G | CA364399144 | MMUT | c.1102G>C (p.Val368Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451696C>T | CA364399145 | MMUT | c.1102G>A (p.Val368Ile) | |
6 | g.49451697A= | CA1627389377 | MMUT | c.1101T= (p.Ile367=) | |
6 | g.49451697A>C | CA364399146 | MMUT | c.1101T>G (p.Ile367Met) | |
6 | g.49451697A>G | CA450606664 | MMUT | c.1101T>C (p.Ile367=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451697A>T | CA450606665 | MMUT | c.1101T>A (p.Ile367=) | |
6 | g.49451698A>C | CA364399152 | MMUT | c.1100T>G (p.Ile367Ser) | |
6 | g.49451698A>G | CA364399151 | MMUT | c.1100T>C (p.Ile367Thr) | gnomAD v4 |
6 | g.49451698A>T | CA364399149 | MMUT | c.1100T>A (p.Ile367Asn) | |
6 | g.49451699T>A | CA364399153 | MMUT | c.1099A>T (p.Ile367Phe) | |
6 | g.49451699T>C | CA364399154 | MMUT | c.1099A>G (p.Ile367Val) | |
6 | g.49451699T>G | CA364399155 | MMUT | c.1099A>C (p.Ile367Leu) | |
6 | g.49451700A= | CA1627389378 | MMUT | c.1098T= (p.Asn366=) | |
6 | g.49451700A>C | CA364399156 | MMUT | c.1098T>G (p.Asn366Lys) | |
6 | g.49451700A>G | CA450606666 | MMUT | c.1098T>C (p.Asn366=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451700A>T | CA364399159 | MMUT | c.1098T>A (p.Asn366Lys) | |
6 | g.49451701T>A | CA364399161 | MMUT | c.1097A>T (p.Asn366Ile) | |
6 | g.49451701T>C | CA347901 | MMUT | c.1097A>G (p.Asn366Ser) | ClinVar dbSNP |
6 | g.49451701T>G | CA364399163 | MMUT | c.1097A>C (p.Asn366Thr) | |
6 | g.49451701T= | CA1627389379 | MMUT | c.1097A= (p.Asn366=) | |
6 | g.49451702T>A | CA364399165 | MMUT | c.1096A>T (p.Asn366Tyr) | |
6 | g.49451702T>C | CA364399166 | MMUT | c.1096A>G (p.Asn366Asp) | |
6 | g.49451702T>G | CA364399167 | MMUT | c.1096A>C (p.Asn366His) | |
6 | g.49451703A>C | CA364399169 | MMUT | c.1095T>G (p.Asn365Lys) | |
6 | g.49451703A>G | CA450606667 | MMUT | c.1095T>C (p.Asn365=) | |
6 | g.49451703A>T | CA364399171 | MMUT | c.1095T>A (p.Asn365Lys) | |
6 | g.49451704T>A | CA364399175 | MMUT | c.1094A>T (p.Asn365Ile) | |
6 | g.49451704T>C | CA364399176 | MMUT | c.1094A>G (p.Asn365Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451704T>G | CA364399174 | MMUT | c.1094A>C (p.Asn365Thr) | |
6 | g.49451704T= | CA1627389380 | MMUT | c.1094A= (p.Asn365=) | |
6 | g.49451705T>A | CA364399177 | MMUT | c.1093A>T (p.Asn365Tyr) | |
6 | g.49451705T>C | CA3846958 | MMUT | c.1093A>G (p.Asn365Asp) | dbSNP ExAC gnomAD v2 |
6 | g.49451705T>G | CA364399179 | MMUT | c.1093A>C (p.Asn365His) | dbSNP gnomAD v3 gnomAD v4 |