Mutation

Primary Site >> Stomach Cancer

Gene >> ROCK2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11216193:11216193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426C>T
AA Mutation	p.Arg476Cys(p.R476C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11215397:11215397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1613A>T
AA Mutation	p.Asp538Val(p.D538V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11287690:11287690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188G>A
AA Mutation	p.Arg63Lys(p.R63K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11208354:11208354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2297G>A
AA Mutation	p.Cys766Tyr(p.C766Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11192332:11192332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3979C>G
AA Mutation	p.Leu1327Val(p.L1327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315872
Start	11218987:11218987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315872
Start	11211790:11211790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11192259:11192259(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4052delA
AA Mutation	p.Lys1351SerfsTer17(p.K1351Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11192271:11192271(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4040delA
AA Mutation	p.Lys1347ArgfsTer21(p.K1347Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11207798:11207817(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2458_2477delCTAAAAATGTCAGAAAAGCA
AA Mutation	p.Leu820ValfsTer6(p.L820Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11249711:11249711(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755738345
CDS Mutation	c.412delT
AA Mutation	p.Trp138GlyfsTer31(p.W138Gfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11235738:11235738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.687delA
AA Mutation	p.Lys229AsnfsTer2(p.K229Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11215374:11215374(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1636delA
AA Mutation	p.Arg546GlufsTer12(p.R546Efs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11227322:11227322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.800delG
AA Mutation	p.Gly267ValfsTer14(p.G267Vfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11198559:11198562(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3028_3031delGAAA
AA Mutation	p.Glu1010Ter(p.E1010*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11344109:11344109(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.28delA
AA Mutation	p.Met10CysfsTer24(p.M10Cfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000315872
Start	11214990:11214990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1786G>T
AA Mutation	p.Glu596Ter(p.E596*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11207810:11207811(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2464dupA
AA Mutation	p.Met822AsnfsTer11(p.M822Nfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000315872
Start	11211679:11211679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2203+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	20
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000315872
Start	11222046:11222093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1089_1099+37delCATAAGAGAAAGTAAGTCAATAAACCTAAATATTTTCATTCCATCACA
Mutation Classification	Splice_Site
Feature Type	Transcript