Mutation

Primary Site >> Stomach Cancer

Gene >> ROCK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	21049814:21049814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242T>C
AA Mutation	p.Val81Ala(p.V81A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	21006592:21006592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644A>T
AA Mutation	p.Glu548Asp(p.E548D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	21042685:21042685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>A
AA Mutation	p.Ala234Thr(p.A234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	20967758:20967758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3186G>A
AA Mutation	p.Met1062Ile(p.M1062I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	20984358:20984358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2482C>T
AA Mutation	p.Leu828Phe(p.L828F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000399799
Start	20986950:20986950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2304A>C
AA Mutation	p.Glu768Asp(p.E768D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	21008070:21008070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1535T>C
AA Mutation	p.Val512Ala(p.V512A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	20955226:20955226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3532C>T
AA Mutation	p.Pro1178Ser(p.P1178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	20959868:20959868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3484T>C
AA Mutation	p.Ser1162Pro(p.S1162P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399799
Start	21042171:21042171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885T>A
AA Mutation	p.Asn295Lys(p.N295K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399799
Start	20984491:20984491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2349G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399799
Start	20984395:20984395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2445G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399799
Start	20953718:20953718(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752898741
CDS Mutation	c.3921delA
AA Mutation	p.Lys1307AsnfsTer3(p.K1307Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399799
Start	21049143:21049143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.363delC
AA Mutation	p.Trp122GlyfsTer31(p.W122Gfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399799
Start	20959900:20959900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3452delT
AA Mutation	p.Leu1151CysfsTer20(p.L1151Cfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399799
Start	20953718:20953719(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3920_3921delAA
AA Mutation	p.Lys1307MetfsTer11(p.K1307Mfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399799
Start	21045461:21045461(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.421delT
AA Mutation	p.Tyr141MetfsTer12(p.Y141Mfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000399799
Start	21042613:21042613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>T
AA Mutation	p.Glu258Ter(p.E258*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000399799
Start	20991283:20991283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2036C>G
AA Mutation	p.Ser679Ter(p.S679*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000399799
Start	20982822:20982822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2500G>T
AA Mutation	p.Gly834Ter(p.G834*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000399799
Start	21006591:21006591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645G>T
AA Mutation	p.Glu549Ter(p.E549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399799
Start	21049143:21049144(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.362dupT
AA Mutation	p.Trp122LeufsTer25(p.W122Lfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000399799
Start	21049779:21049779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	24
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000399799
Start	21045324:21045325(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.557_558insTTT
AA Mutation	p.Ala185_Leu186insPhe(p.A185_L186insF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript