Colon Cancer: Gene >> ROCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11208318:11208318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2333T>C
AA Mutation	p.Leu778Pro(p.L778P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11235748:11235748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677G>A
AA Mutation	p.Gly226Glu(p.G226E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11192624:11192624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3776A>T
AA Mutation	p.Lys1259Met(p.K1259M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11216178:11216178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441G>A
AA Mutation	p.Ala481Thr(p.A481T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11249704:11249704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419A>G
AA Mutation	p.Glu140Gly(p.E140G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11211799:11211799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2085A>C
AA Mutation	p.Lys695Asn(p.K695N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11222166:11222166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339Gln(p.R339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11287678:11287678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200A>C
AA Mutation	p.Asn67Thr(p.N67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11201020:11201020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2847G>T
AA Mutation	p.Glu949Asp(p.E949D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11197619:11197619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3186G>T
AA Mutation	p.Glu1062Asp(p.E1062D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11192254:11192254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4057C>A
AA Mutation	p.Pro1353Thr(p.P1353T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315872
Start	11211760:11211760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315872
Start	11224342:11224342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315872
Start	11198763:11198763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2922T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315872
Start	11215589:11215589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753996403
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
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

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11286619:11286619(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.244delA
AA Mutation	p.Ile82SerfsTer6(p.I82Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
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

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11211834:11211834(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2050delA
AA Mutation	p.Ser684AlafsTer5(p.S684Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000315872
Start	11197537:11197537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3268G>T
AA Mutation	p.Glu1090Ter(p.E1090*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000315872
Start	11201347:11201347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2686G>T
AA Mutation	p.Glu896Ter(p.E896*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000315872
Start	11214932:11214933(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1833_1843dupTGCCAAGTTAA
AA Mutation	p.Lys615MetfsTer4(p.K615Mfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ROCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11192284:11192284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4027C>T
AA Mutation	p.Arg1343Trp(p.R1343W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11194317:11194317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3547C>T
AA Mutation	p.Leu1183Phe(p.L1183F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11202072:11202072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2599G>A
AA Mutation	p.Glu867Lys(p.E867K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11211748:11211748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2136G>T
AA Mutation	p.Lys712Asn(p.K712N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11211735:11211735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2149G>A
AA Mutation	p.Asp717Asn(p.D717N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315872
Start	11227358:11227358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764A>T
AA Mutation	p.Asp255Val(p.D255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315872
Start	11215521:11215521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1586delT
AA Mutation	p.Leu529TrpfsTer8(p.L529Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000315872
Start	11198714:11198714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2971G>T
AA Mutation	p.Glu991Ter(p.E991*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000315872
Start	11207787:11207787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2488G>T
AA Mutation	p.Glu830Ter(p.E830*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript