Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRAPPC9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139732005:139732005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3253G>T
AA Mutation	p.Gly1085Cys(p.G1085C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139988793:139988793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141596857
CDS Mutation	c.2743G>A
AA Mutation	p.Glu915Lys(p.E915K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140405593:140405593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992T>G
AA Mutation	p.Ile331Ser(p.I331S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140371029:140371029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286A>T
AA Mutation	p.Tyr429Phe(p.Y429F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140435166:140435166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779077167
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Trp(p.R269W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139732023:139732023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3235G>A
AA Mutation	p.Asp1079Asn(p.D1079N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140451142:140451142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762840909
CDS Mutation	c.232G>A
AA Mutation	p.Val78Met(p.V78M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139731221:139731221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3287C>T
AA Mutation	p.Pro1096Leu(p.P1096L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139731167:139731167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3341T>C
AA Mutation	p.Phe1114Ser(p.F1114S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139910164:139910164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770440531
CDS Mutation	c.2947G>A
AA Mutation	p.Gly983Ser(p.G983S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140371089:140371089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409His(p.R409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140450989:140450989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368666913
CDS Mutation	c.385C>T
AA Mutation	p.Arg129Cys(p.R129C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139988778:139988778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555371576
CDS Mutation	c.2758G>A
AA Mutation	p.Val920Ile(p.V920I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140300583:140300583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762751827
CDS Mutation	c.1654C>T
AA Mutation	p.Leu552Phe(p.L552F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140311278:140311278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768262663
CDS Mutation	c.1592C>T
AA Mutation	p.Pro531Leu(p.P531L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139910226:139910226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2885A>G
AA Mutation	p.Asn962Ser(p.N962S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140371084:140371084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231G>A
AA Mutation	p.Ala411Thr(p.A411T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140439171:140439171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611G>A
AA Mutation	p.Arg204His(p.R204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140451150:140451150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757282308
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	139731209:139731209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199842078
CDS Mutation	c.3299C>T
AA Mutation	p.Ser1100Leu(p.S1100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	140451323:140451323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764844525
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	139732096:139732096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555520602
CDS Mutation	c.3162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	140023993:140023993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2643T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000438773
Start	139731195:139731195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3313delG
AA Mutation	p.Ala1105ProfsTer127(p.A1105Pfs*127)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000438773
Start	140300548:140300549(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1688_1689insTGCACATGCAT
AA Mutation	p.Gln563HisfsTer5(p.Q563Hfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000438773
Start	140311345:140311350(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1520_1525delTAGAGA
AA Mutation	p.Leu507_Asn509delinsHis(p.L507_N509delinsH)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRAPPC9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140275801:140275801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2135C>A
AA Mutation	p.Pro712His(p.P712H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140024048:140024048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2588C>G
AA Mutation	p.Ser863Cys(p.S863C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140287631:140287631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190087909
CDS Mutation	c.1958C>T
AA Mutation	p.Thr653Met(p.T653M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140451214:140451214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160T>A
AA Mutation	p.Tyr54Asn(p.Y54N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000438773
Start	140439157:140439157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625G>A
AA Mutation	p.Val209Met(p.V209M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	140275677:140275677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760537145
CDS Mutation	c.2259G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	140405652:140405652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367765204
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	140284002:140284002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438773
Start	140284011:140284011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992C>T
Mutation Classification	Silent
Feature Type	Transcript