Colon Cancer: Gene >> ATAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376485
Start	30642906:30642906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863A>C
AA Mutation	p.Glu288Ala(p.E288A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376485
Start	30643004:30643004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Cys(p.R321C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376485
Start	30646067:30646067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1049G>A
AA Mutation	p.Gly350Asp(p.G350D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376485
Start	30642957:30642957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914G>A
AA Mutation	p.Arg305His(p.R305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376485
Start	30642820:30642820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370091331
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376485
Start	30642937:30642937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.899delC
AA Mutation	p.Pro300HisfsTer31(p.P300Hfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376485
Start	30645943:30645944(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs200190404
CDS Mutation	c.1024dupG
AA Mutation	p.Val342GlyfsTer23(p.V342Gfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	start_lost
Transcription ID	ENST00000376485
Start	30626887:30626887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ATAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376485
Start	30646521:30646521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144A>G
AA Mutation	p.Met382Val(p.M382V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376485
Start	30642979:30642980(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.941dupG
AA Mutation	p.Ser315GlnfsTer50(p.S315Qfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript