Colon Cancer: Gene >> ATG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343245
Start	106316177:106316177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32T>C
AA Mutation	p.Val11Ala(p.V11A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343245
Start	106201975:106201975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>A
AA Mutation	p.Glu230Lys(p.E230K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343245
Start	106186575:106186575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793C>A
AA Mutation	p.Leu265Ile(p.L265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343245
Start	106316193:106316193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16G>T
AA Mutation	p.Asp6Tyr(p.D6Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343245
Start	106186664:106186664(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.704delA
AA Mutation	p.Lys235ArgfsTer4(p.K235Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343245
Start	106186663:106186664(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.704dupA
AA Mutation	p.Asn236GlufsTer9(p.N236Efs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ATG5

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000343245
Start	106279709:106279709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>T
AA Mutation	p.Glu144Ter(p.E144*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript