Colon Cancer: Gene >> GPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340124
Start	46900745:46900745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752970046
CDS Mutation	c.397A>C
AA Mutation	p.Lys133Gln(p.K133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340124
Start	46897696:46897696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292G>A
AA Mutation	p.Ala98Thr(p.A98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340124
Start	46909708:46909708(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.605delG
AA Mutation	p.Gly202AlafsTer8(p.G202Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340124
Start	46922319:46922319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115C>T
AA Mutation	p.Ser372Leu(p.S372L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340124
Start	46900757:46900757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768172166
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Trp(p.R137W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340124
Start	46924496:46924496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753982355
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript