Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARHGAP35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919312:46919312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46937330:46937330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3748C>T
AA Mutation	p.Pro1250Ser(p.P1250S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921023:46921023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348G>A
AA Mutation	p.Arg783Gln(p.R783Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46922316:46922316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3641G>A
AA Mutation	p.Arg1214Gln(p.R1214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46918950:46918950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275A>G
AA Mutation	p.His92Arg(p.H92R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919951:46919951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564899532
CDS Mutation	c.1276G>A
AA Mutation	p.Glu426Lys(p.E426K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46988036:46988036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760436977
CDS Mutation	c.3874A>G
AA Mutation	p.Met1292Val(p.M1292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	47000443:47000443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768711914
CDS Mutation	c.4255C>T
AA Mutation	p.Arg1419Cys(p.R1419C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46920905:46920905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761081196
CDS Mutation	c.2230C>T
AA Mutation	p.Arg744Cys(p.R744C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919298:46919298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623G>A
AA Mutation	p.Arg208Gln(p.R208Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919654:46919654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199897795
CDS Mutation	c.979C>T
AA Mutation	p.Arg327Cys(p.R327C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46999363:46999363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4096A>G
AA Mutation	p.Lys1366Glu(p.K1366E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46989588:46989588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3949G>A
AA Mutation	p.Val1317Met(p.V1317M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46922130:46922130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3455T>C
AA Mutation	p.Val1152Ala(p.V1152A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921487:46921487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2812T>G
AA Mutation	p.Phe938Val(p.F938V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46922115:46922115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3440G>A
AA Mutation	p.Arg1147His(p.R1147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46999330:46999330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4063C>T
AA Mutation	p.His1355Tyr(p.H1355Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919253:46919253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578A>C
AA Mutation	p.Lys193Thr(p.K193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921236:46921236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2561G>T
AA Mutation	p.Gly854Val(p.G854V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919381:46919381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706G>A
AA Mutation	p.Val236Met(p.V236M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46920619:46920619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1944G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46920874:46920874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2199C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46922125:46922125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	47000604:47000604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185820645
CDS Mutation	c.4416G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46920685:46920685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46919086:46919086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368641937
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46921993:46921993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46919680:46919680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	47000355:47000355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4167T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46921245:46921245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2575delT
AA Mutation	p.Tyr859IlefsTer28(p.Y859Ifs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46919679:46919679(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1004delG
AA Mutation	p.Arg335LeufsTer12(p.R335Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46921484:46921484(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2814delT
AA Mutation	p.Phe938LeufsTer10(p.F938Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404338
Start	46921503:46921503(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2834delA
AA Mutation	p.Lys945ArgfsTer3(p.K945Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46922108:46922108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3433C>T
AA Mutation	p.Arg1145Ter(p.R1145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46921046:46921046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2371G>T
AA Mutation	p.Gly791Ter(p.G791*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46919936:46919936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>T
AA Mutation	p.Glu421Ter(p.E421*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919662:46919662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987G>T
AA Mutation	p.Lys329Asn(p.K329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919777:46919777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102A>C
AA Mutation	p.Lys368Gln(p.K368Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921442:46921442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2767C>A
AA Mutation	p.Pro923Thr(p.P923T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919364:46919364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689C>T
AA Mutation	p.Ala230Val(p.A230V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46919873:46919873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198G>A
AA Mutation	p.Glu400Lys(p.E400K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921665:46921665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2990G>A
AA Mutation	p.Arg997Gln(p.R997Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46999353:46999353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4086G>T
AA Mutation	p.Lys1362Asn(p.K1362N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46920844:46920844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2169A>C
AA Mutation	p.Gln723His(p.Q723H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404338
Start	46921529:46921529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2854C>A
AA Mutation	p.His952Asn(p.H952N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404338
Start	46989656:46989656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4017C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000404338
Start	46921664:46921664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Ter(p.R997*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript