Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZFP36L2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225373:43225373(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.431delG
AA Mutation	p.Gly144AlafsTer43(p.G144Afs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225502:43225511(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.293_302delACGGCACCCT
AA Mutation	p.Tyr98LeufsTer86(p.Y98Lfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225512:43225513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.291_292delCT
AA Mutation	p.Tyr98ArgfsTer4(p.Y98Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225286:43225287(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.517_518delAA
AA Mutation	p.Lys173ValfsTer300(p.K173Vfs*300)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225484:43225484(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs765083004
CDS Mutation	c.320delG
AA Mutation	p.Gly107AlafsTer80(p.G107Afs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225199:43225202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.602_605delATAC
AA Mutation	p.His201ProfsTer259(p.H201Pfs*259)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225532:43225539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.265_272delAGCGCGGC
AA Mutation	p.Ser89GlyfsTer11(p.S89Gfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000282388
Start	43225362:43225362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
AA Mutation	p.Gln148Ter(p.Q148*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225162:43225163(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.641dupT
AA Mutation	p.Ile215HisfsTer259(p.I215Hfs*259)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225372:43225373(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.431dupG
AA Mutation	p.Gly145ArgfsTer329(p.G145Rfs*329)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225449:43225450(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.354dupA
AA Mutation	p.Phe119IlefsTer7(p.F119Ifs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225352:43225353(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.451_452insA
AA Mutation	p.Ser151TyrfsTer323(p.S151Yfs*323)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225498:43225499(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.305dupA
AA Mutation	p.Glu103GlyfsTer23(p.E103Gfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225393:43225394(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.410dupT
AA Mutation	p.Gln138AlafsTer336(p.Q138Afs*336)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225319:43225320(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.478_484dupCGGCCCT
AA Mutation	p.Phe162SerfsTer314(p.F162Sfs*314)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225483:43225484(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749991294
CDS Mutation	c.320dupG
AA Mutation	p.Gly108ArgfsTer18(p.G108Rfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225496:43225497(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.307dupG
AA Mutation	p.Glu103GlyfsTer23(p.E103Gfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_lost
Transcription ID	ENST00000282388
Start	43224321:43224321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483T>A
AA Mutation	p.Ter495ArgextTer81(p.495Rext81)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP36L2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225325:43225326(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.478dupC
AA Mutation	p.Arg160ProfsTer314(p.R160Pfs*314)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225203:43225204(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.600dupT
AA Mutation	p.His201SerfsTer273(p.H201Sfs*273)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225300:43225301(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.503dupG
AA Mutation	p.Cys168TrpfsTer306(p.C168Wfs*306)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225442:43225443(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.361dupG
AA Mutation	p.Asp121GlyfsTer5(p.D121Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282388
Start	43225185:43225186(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.617_618dupGC
AA Mutation	p.Pro207AlafsTer255(p.P207Afs*255)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript