Colon Cancer: Gene >> IDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340855
Start	149503428:149503428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340855
Start	149486969:149486969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136C>G
AA Mutation	p.Pro379Arg(p.P379R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340855
Start	149483114:149483114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781916566
CDS Mutation	c.1285G>A
AA Mutation	p.Val429Ile(p.V429I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340855
Start	149503477:149503477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113993949
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000340855
Start	149496348:149496348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.877C>A
AA Mutation	p.Gln293Lys(p.Q293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340855
Start	149503393:149503393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337G>A
AA Mutation	p.Ala113Thr(p.A113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340855
Start	149487036:149487036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069G>A
AA Mutation	p.Val357Ile(p.V357I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000340855
Start	149498301:149498301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894860
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Ter(p.R172*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000340855
Start	149496517:149496517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IDS

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340855
Start	149503409:149503409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321C>G
Mutation Classification	Silent
Feature Type	Transcript