| 212 | Amplification | | transcript_amplification |
| 931 | C420R RS121913272,CYS420ARG | NM_006218.3:c.1258T>C,NP_006209.2:p.Cys420Arg,NC_000003.11:g.178927980T>C,ENST00000263967.3:c.1258T>C | missense_variant |
| 3337 | C604R | | |
| 1653 | D350G ASP350GLY | ENST00000263967.3:c.1049A>G,NC_000003.11:g.178921567A>G,NM_006218.2:c.1049A>G,NP_006209.2:p.Asp350Gly | missense_variant |
| 3338 | D350N | | |
| 5240 | E453A | | |
| 5241 | E453D | | |
| 5242 | E453G | | |
| 1177 | E453K | | missense_variant |
| 1205 | E453Q | | missense_variant |
| 5243 | E453V | | |
| 5219 | E542A | | |
| 5220 | E542D | | |
| 5221 | E542G | | |
| 103 | E542K GLU542LYS,RS121913273 | NM_006218.3:c.1624G>A,NP_006209.2:p.Glu542Lys,ENST00000263967.3:c.1624G>A,NC_000003.11:g.178936082G>A | missense_variant |
| 933 | E542Q RS121913273,GLU542GLN | NM_006218.3:c.1624G>C,NP_006209.2:p.Glu542Gln,NC_000003.11:g.178936082G>C,ENST00000263967.3:c.1624G>C | missense_variant |
| 5222 | E542R | | |
| 5223 | E542V | | |
| 882 | E545A RS121913274,GLU545ALA | NM_006218.3:c.1634A>C,NP_006209.2:p.Glu545Ala,NC_000003.11:g.178936092A>C,ENST00000263967.3:c.1634A>C | missense_variant |
| 934 | E545D RS121913275,GLU545ASP | NM_006218.3:c.1635G>C,NP_006209.2:p.Glu545Asp,NC_000003.11:g.178936093G>C,ENST00000263967.3:c.1635G>C | missense_variant |
| 883 | E545G RS121913274,GLU545GLY | NM_006218.3:c.1634A>G,NP_006209.2:p.Glu545Gly,NC_000003.11:g.178936092A>G,ENST00000263967.3:c.1634A>G | missense_variant |
| 104 | E545K GLU545LYS,RS104886003 | NM_006218.3:c.1633G>A,NP_006209.2:p.Glu545Lys,ENST00000263967.3:c.1633G>A,NC_000003.11:g.178936091G>A | missense_variant |
| 5256 | E545L | | |
| 881 | E545Q RS104886003,GLU545GLN | NM_006218.3:c.1633G>C,NP_006209.2:p.Glu545Gln,NC_000003.11:g.178936091G>C,ENST00000263967.3:c.1633G>C | missense_variant |
| 5257 | E545R | | |
| 884 | E545V RS121913274,GLU545VAL | NM_006218.3:c.1634A>T,NP_006209.2:p.Glu545Val,NC_000003.11:g.178936092A>T,ENST00000263967.3:c.1634A>T | missense_variant |
| 1500 | E81K GLU81LYS,RS1057519929 | NM_006218.3:c.241G>A,NP_006209.2:p.Glu81Lys,NC_000003.11:g.178916854G>A,ENST00000263967.3:c.241G>A | missense_variant |
| 106 | Exon 10 Mutation EXON 9 MUTATION | | exon_variant |
| 105 | Exon 21 Mutation EXON 20 MUTATION | | exon_variant |
| 3667 | F930S | | |
| 3437 | G1007R | | |
| 1501 | G1049A GLY1049ALA | ENST00000263967.3:c.3146G>C,NC_000003.11:g.178952091G>C,NM_006218.2:c.3146G>C,NP_006209.2:p.Gly1049Ala | missense_variant |
| 5231 | G1049C | | |
| 5232 | G1049D | | |
| 940 | G1049R RS121913277,GLY1049ARG | NM_006218.3:c.3145G>C,NP_006209.2:p.Gly1049Arg,NC_000003.11:g.178952090G>C,ENST00000263967.3:c.3145G>C | missense_variant |
| 939 | G1049S RS121913277,GLY1049SER | NM_006218.3:c.3145G>A,NP_006209.2:p.Gly1049Ser,NC_000003.11:g.178952090G>A,ENST00000263967.3:c.3145G>A | missense_variant |
| 5228 | G106A | | |
| 5229 | G106D | | |
| 1201 | G106R | | missense_variant |
| 5227 | G106S | | |
| 1179 | G106V | | missense_variant |
| 5230 | G118D | | |
| 5213 | H1047D | | |
| 5214 | H1047I | | |
| 1151 | H1047L RS121913279,HIS1047LEU | NM_006218.3:c.3140A>T,NP_006209.2:p.His1047Leu,NC_000003.11:g.178952085A>T,ENST00000263967.3:c.3140A>T | missense_variant |
| 5215 | H1047N | | |
| 5216 | H1047P | | |
| 5217 | H1047Q | | |
| 107 | H1047R HIS1047ARG,RS121913279 | NM_006218.3:c.3140A>G,NP_006209.2:p.His1047Arg,ENST00000263967.3:c.3140A>G,NC_000003.11:g.178952085A>G | missense_variant |
| 5218 | H1047T | | |
| 938 | H1047Y RS121913281,HIS1047TYR | NM_006218.3:c.3139C>T,NP_006209.2:p.His1047Tyr,NC_000003.11:g.178952084C>T,ENST00000263967.3:c.3139C>T | missense_variant |
| 1235 | I391M ILE391MET,RS2230461 | NM_006218.3:c.1173A>G,NP_006209.2:p.Ile391Met,NC_000003.11:g.178927410A>G,ENST00000263967.3:c.1173A>G | missense_variant |
| 1202 | K111E | | missense_variant |
| 1234 | K111N LYS111ASN,RS1057519934 | NM_006218.3:c.333G>C,NP_006209.2:p.Lys111Asn,NC_000003.11:g.178916946G>C,ENST00000263967.3:c.333G>C | missense_variant |
| 5224 | K111R | | |
| 3666 | K944N | | |
| 3669 | K966E | | |
| 3670 | L938* | | |
| 937 | M1043I RS121913283,MET1043ILE | NM_006218.3:c.3129G>T,NP_006209.2:p.Met1043Ile,NC_000003.11:g.178952074G>T,ENST00000263967.3:c.3129G>T | missense_variant |
| 5239 | M1043T | | |
| 936 | M1043V | | missense_variant |
| 311 | Mutation | | gain_of_function_variant,transcript_variant |
| 3438 | N1044K | | |
| 5233 | N345D | | |
| 5234 | N345H | | |
| 5235 | N345I | | |
| 930 | N345K RS121913284,ASN345LYS | NM_006218.3:c.1035T>A,NP_006209.2:p.Asn345Lys,NC_000003.11:g.178921553T>A,ENST00000263967.3:c.1035T>A | missense_variant |
| 5236 | N345S | | |
| 5237 | N345T | | |
| 5238 | N345Y | | |
| 2362 | Overexpression | | |
| 294 | P471L PRO471LEU,RS1057519872 | NC_000003.11:g.178928226C>T,ENST00000263967.3:c.1412C>T,NM_006218.3:c.1412C>T,NP_006209.2:p.Pro471Leu | missense_variant |
| 886 | Q546E RS121913286,GLN546GLU | NM_006218.3:c.1636C>G,NP_006209.2:p.Gln546Glu,NC_000003.11:g.178936094C>G,ENST00000263967.3:c.1636C>G | missense_variant |
| 5226 | Q546H | | |
| 885 | Q546K RS121913286,GLN546LYS | NM_006218.3:c.1636C>A,NP_006209.2:p.Gln546Lys,NC_000003.11:g.178936094C>A,ENST00000263967.3:c.1636C>A | missense_variant |
| 889 | Q546L | | missense_variant |
| 887 | Q546P GLN546PRO | NC_000003.11:g.178936095A>C,NC_000003.12:g.179218307A>C,NM_006218.4:c.1637A>C,NP_006209.2:p.Gln546Pro | missense_variant |
| 888 | Q546R | NC_000003.11:g.178936095A>G,NC_000003.12:g.179218307A>G,NP_006209.2:p.Gln546Arg,NM_006218.4:c.1637A>G | missense_variant |
| 929 | R88Q RS121913287,ARG88GLN | NC_000003.12:g.179199088G>A,NC_000003.11:g.178916876G>A,NM_006218.4:c.263G>A,NP_006209.2:p.Arg88Gln | missense_variant |
| 1178 | R93W ARG93TRP | ENST00000263967.3:c.277C>T,NC_000003.11:g.178916890C>T,NM_006218.2:c.277C>T,NP_006209.2:p.Arg93Trp | missense_variant |
| 3222 | Rare Mutation | | |
| 1499 | S158L SER158LEU | ENST00000263967.3:c.473C>T,NC_000003.11:g.178917598C>T,NM_006218.2:c.473C>T,NP_006209.2:p.Ser158Leu | missense_variant |
| 3668 | V955G | | |
| 3001 | V955I VAL955ILE | NC_000003.11:g.178948091G>A,NM_006218.2:c.2863G>A,ENST00000263967.3:c.2863G>A,NP_006209.2:p.Val955Ile | missense_variant |
| 2590 | Wildtype | | wild_type |