Colon Cancer: Gene >> TDG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392872
Start	103983172:103983172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651G>T
AA Mutation	p.Gln217His(p.Q217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392872
Start	103982873:103982873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553T>A
AA Mutation	p.Tyr185Asn(p.Y185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392872
Start	103986971:103986971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114G>A
AA Mutation	p.Glu372Lys(p.E372K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392872
Start	103979917:103979917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253T>C
AA Mutation	p.Ser85Pro(p.S85P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392872
Start	103979909:103979910(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs762845105
CDS Mutation	c.252dupA
AA Mutation	p.Ser85IlefsTer19(p.S85Ifs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TDG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392872
Start	103985656:103985656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018G>T
AA Mutation	p.Ala340Ser(p.A340S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392872
Start	103987015:103987015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158G>C
AA Mutation	p.Gln386His(p.Q386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript