Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IGSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159927365:159927365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3520G>A
AA Mutation	p.Glu1174Lys(p.E1174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159927400:159927400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745423827
CDS Mutation	c.3485G>A
AA Mutation	p.Arg1162Gln(p.R1162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159942983:159942983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757719031
CDS Mutation	c.227G>A
AA Mutation	p.Arg76Gln(p.R76Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159931470:159931470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761536687
CDS Mutation	c.1496C>T
AA Mutation	p.Thr499Met(p.T499M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159927449:159927449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763910745
CDS Mutation	c.3436C>T
AA Mutation	p.Arg1146Trp(p.R1146W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159931596:159931596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200623535
CDS Mutation	c.1370G>A
AA Mutation	p.Arg457Gln(p.R457Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159932610:159932610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527258901
CDS Mutation	c.1147G>A
AA Mutation	p.Ala383Thr(p.A383T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159927427:159927427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3458G>A
AA Mutation	p.Arg1153His(p.R1153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159943029:159943029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Gly61Arg(p.G61R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159937761:159937761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781724050
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Cys(p.R109C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159931465:159931465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760853772
CDS Mutation	c.1501G>A
AA Mutation	p.Val501Ile(p.V501I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159928752:159928752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552997339
CDS Mutation	c.2636G>A
AA Mutation	p.Arg879His(p.R879H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159943000:159943000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573559309
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159930711:159930711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159930792:159930792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201379431
CDS Mutation	c.1713G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159927357:159927357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3528C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159930411:159930411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1842G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159931532:159931532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754561359
CDS Mutation	c.1434G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368094
Start	159928487:159928487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2901T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159928924:159928924(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2464delG
AA Mutation	p.Asp822IlefsTer33(p.D822Ifs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159930338:159930338(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1915delG
AA Mutation	p.Val639TyrfsTer114(p.V639Yfs*114)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159943056:159943056(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753928344
CDS Mutation	c.154delC
AA Mutation	p.Leu52CysfsTer79(p.L52Cfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159934273:159934273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1021delG
AA Mutation	p.Val341Ter(p.V341*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159934242:159934242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772530564
CDS Mutation	c.1052delC
AA Mutation	p.Pro351HisfsTer30(p.P351Hfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159928662:159928662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2726delC
AA Mutation	p.Pro909LeufsTer19(p.P909Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000368094
Start	159943149:159943149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>T
AA Mutation	p.Arg21Ter(p.R21*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000368094
Start	159931515:159931515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451G>A
AA Mutation	p.Trp484Ter(p.W484*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368094
Start	159943055:159943056(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764250808
CDS Mutation	c.154dupC
AA Mutation	p.Leu52ProfsTer27(p.L52Pfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IGSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159930716:159930716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789G>A
AA Mutation	p.Glu597Lys(p.E597K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159927365:159927365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3520G>A
AA Mutation	p.Glu1174Lys(p.E1174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368094
Start	159928188:159928188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770700069
CDS Mutation	c.3200G>A
AA Mutation	p.Arg1067Gln(p.R1067Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript