Colon Cancer: Gene >> ASNS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000175506
Start	97859254:97859254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>T
AA Mutation	p.Pro211Leu(p.P211L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000175506
Start	97859376:97859376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000175506
Start	97859373:97859373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755945639
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000175506
Start	97853355:97853355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1270C>T
AA Mutation	p.Arg424Ter(p.R424*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ASNS

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000175506
Start	97853117:97853117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1419A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000175506
Start	97868970:97868970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373645939
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Ter(p.R63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000175506
Start	97858956:97858956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript