Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARHGEF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156938504:156938504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3986C>T
AA Mutation	p.Ala1329Val(p.A1329V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156946155:156946155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2582A>G
AA Mutation	p.Glu861Gly(p.E861G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156942775:156942775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746467759
CDS Mutation	c.3121C>T
AA Mutation	p.Arg1041Trp(p.R1041W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156963575:156963575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863A>C
AA Mutation	p.Lys288Thr(p.K288T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156969302:156969302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755443263
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Cys(p.R229C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156937460:156937460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4109C>T
AA Mutation	p.Pro1370Leu(p.P1370L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156942771:156942771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3125C>T
AA Mutation	p.Ala1042Val(p.A1042V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361409
Start	156961678:156961678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768597800
CDS Mutation	c.1118C>T
AA Mutation	p.Ala373Val(p.A373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156959130:156959130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368227122
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392Gln(p.R392Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156984426:156984426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Cys(p.R46C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156980466:156980466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Gly82Ser(p.G82S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361409
Start	156936895:156936895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4431C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361409
Start	156969291:156969291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361409
Start	156969351:156969351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.636C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361409
Start	156980452:156980452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751727111
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361409
Start	156937477:156937477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361409
Start	156969329:156969329(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.658delG
AA Mutation	p.Asp220ThrfsTer18(p.D220Tfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361409
Start	156954900:156954900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1670delC
AA Mutation	p.Pro557LeufsTer9(p.P557Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361409
Start	156937418:156937418(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4151delC
AA Mutation	p.Pro1384LeufsTer41(p.P1384Lfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361409
Start	156936044:156936044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4525delC
AA Mutation	p.Leu1509TrpfsTer149(p.L1509Wfs*149)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000361409
Start	156946682:156946682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2554C>T
AA Mutation	p.Arg852Ter(p.R852*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000361409
Start	156956500:156956500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471C>T
AA Mutation	p.Arg491Ter(p.R491*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361409
Start	156955702:156955702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1648+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156941395:156941395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3371C>A
AA Mutation	p.Pro1124His(p.P1124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361409
Start	156946138:156946138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2599C>T
AA Mutation	p.Arg867Trp(p.R867W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript