Mutation

Primary Site >> Stomach Cancer

Gene >> MYH11

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15753465:15753465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770613752
CDS Mutation	c.1793C>T
AA Mutation	p.Pro598Leu(p.P598L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15741666:15741666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2656A>G
AA Mutation	p.Thr886Ala(p.T886A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15786648:15786648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>T
AA Mutation	p.Lys205Asn(p.K205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15735471:15735471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3401G>T
AA Mutation	p.Arg1134Met(p.R1134M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15741846:15741846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2566G>A
AA Mutation	p.Ala856Thr(p.A856T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15735477:15735477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3395C>T
AA Mutation	p.Ala1132Val(p.A1132V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15741847:15741847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2565G>C
AA Mutation	p.Gln855His(p.Q855H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15735470:15735470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3402G>C
AA Mutation	p.Arg1134Ser(p.R1134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15837961:15837961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773587055
CDS Mutation	c.292G>A
AA Mutation	p.Glu98Lys(p.E98K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15748093:15748093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2134C>T
AA Mutation	p.Arg712Trp(p.R712W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15718349:15718349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5261C>T
AA Mutation	p.Ala1754Val(p.A1754V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15741813:15741813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745429737
CDS Mutation	c.2599C>T
AA Mutation	p.Arg867Trp(p.R867W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15719671:15719671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4996G>A
AA Mutation	p.Ala1666Thr(p.A1666T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15717306:15717306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5338G>A
AA Mutation	p.Ala1780Thr(p.A1780T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15720972:15720972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4658A>G
AA Mutation	p.Asp1553Gly(p.D1553G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15759685:15759685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431His(p.R431H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15724322:15724322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764341540
CDS Mutation	c.4204G>A
AA Mutation	p.Glu1402Lys(p.E1402K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15737599:15737599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3143A>C
AA Mutation	p.Lys1048Thr(p.K1048T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15720162:15720162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369409348
CDS Mutation	c.4942C>T
AA Mutation	p.Arg1648Cys(p.R1648C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15724673:15724673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769227102
CDS Mutation	c.4090C>T
AA Mutation	p.Arg1364Cys(p.R1364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15738684:15738684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376622843
CDS Mutation	c.3002G>A
AA Mutation	p.Arg1001Gln(p.R1001Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15724278:15724278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4248T>G
AA Mutation	p.Asp1416Glu(p.D1416E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15748153:15748153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2074G>A
AA Mutation	p.Ala692Thr(p.A692T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15759652:15759652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1325A>G
AA Mutation	p.Lys442Arg(p.K442R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000300036
Start	15704077:15704077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751862398
CDS Mutation	c.5833C>T
AA Mutation	p.Arg1945Cys(p.R1945C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300036
Start	15726995:15726995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576890377
CDS Mutation	c.3711C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300036
Start	15704114:15704114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149529195
CDS Mutation	c.5796C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300036
Start	15719303:15719303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776142323
CDS Mutation	c.5088C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300036
Start	15721626:15721626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4374C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300036
Start	15838067:15838067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300036
Start	15714962:15714962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372173243
CDS Mutation	c.5733G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300036
Start	15747679:15747679(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2302delA
AA Mutation	p.Ile768SerfsTer11(p.I768Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000300036
Start	15724718:15724718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4045C>T
AA Mutation	p.Gln1349Ter(p.Q1349*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000300036
Start	15759629:15759629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348C>T
AA Mutation	p.Gln450Ter(p.Q450*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000300036
Start	15726938:15726943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3763_3768delAAGAAG
AA Mutation	p.Lys1255_Lys1256del(p.K1255_K1256del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript