Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042140:119042140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3380G>T
AA Mutation	p.Arg1127Ile(p.R1127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042170:119042170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768823906
CDS Mutation	c.3350G>A
AA Mutation	p.Arg1117Gln(p.R1117Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119058221:119058221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571His(p.R571H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042339:119042339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3181C>T
AA Mutation	p.Arg1061Cys(p.R1061C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119073012:119073012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>T
AA Mutation	p.Arg140Leu(p.R140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119050529:119050529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2465T>C
AA Mutation	p.Met822Thr(p.M822T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119065514:119065514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755084308
CDS Mutation	c.1007C>T
AA Mutation	p.Thr336Met(p.T336M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119065484:119065484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037G>T
AA Mutation	p.Gly346Val(p.G346V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119049850:119049850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2609G>A
AA Mutation	p.Arg870Gln(p.R870Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119061283:119061283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168C>A
AA Mutation	p.Leu390Ile(p.L390I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119037127:119037127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3911G>A
AA Mutation	p.Arg1304His(p.R1304H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042291:119042291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375388729
CDS Mutation	c.3229C>T
AA Mutation	p.Arg1077Trp(p.R1077W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042380:119042380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3140G>A
AA Mutation	p.Gly1047Glu(p.G1047E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042641:119042641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775041698
CDS Mutation	c.2879G>A
AA Mutation	p.Arg960His(p.R960H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119059640:119059640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770069171
CDS Mutation	c.1405C>T
AA Mutation	p.Arg469Trp(p.R469W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119073776:119073776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211T>G
AA Mutation	p.Leu71Val(p.L71V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119051263:119051263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2255G>A
AA Mutation	p.Arg752Gln(p.R752Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119056962:119056962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2056G>A
AA Mutation	p.Glu686Lys(p.E686K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119069600:119069600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796C>A
AA Mutation	p.Pro266Thr(p.P266T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119072916:119072916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119036199:119036199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3989T>C
AA Mutation	p.Val1330Ala(p.V1330A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119065517:119065517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199796475
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335His(p.R335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119059282:119059282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559G>T
AA Mutation	p.Arg520Ile(p.R520I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119037156:119037156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119049822:119049822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201904104
CDS Mutation	c.2637C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369144
Start	119036135:119036135(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4053delA
AA Mutation	p.Glu1352ArgfsTer43(p.E1352Rfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000369144
Start	119036146:119036146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4042G>T
AA Mutation	p.Glu1348Ter(p.E1348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369144
Start	119073565:119073566(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.252_253insCCCACATACC
AA Mutation	p.Ser85ProfsTer10(p.S85Pfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000369144
Start	119038312:119038314(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3652_3654delGAG
AA Mutation	p.Glu1218del(p.E1218del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000369144
Start	119073045:119073047(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.384_386delCCT
AA Mutation	p.Leu129del(p.L129del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042080:119042080(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	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119037215:119037215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3823C>A
AA Mutation	p.Arg1275Ser(p.R1275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119037218:119037218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745913298
CDS Mutation	c.3820C>T
AA Mutation	p.Arg1274Cys(p.R1274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119065421:119065421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367Gln(p.R367Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119037154:119037154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3884G>A
AA Mutation	p.Arg1295Gln(p.R1295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119042431:119042431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138563024
CDS Mutation	c.3089G>A
AA Mutation	p.Arg1030Gln(p.R1030Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119049962:119049962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2497G>A
AA Mutation	p.Glu833Lys(p.E833K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369144
Start	119050625:119050625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772554138
CDS Mutation	c.2369G>A
AA Mutation	p.Arg790Gln(p.R790Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119050585:119050585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2409G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369144
Start	119057980:119057980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1953A>G
Mutation Classification	Silent
Feature Type	Transcript