Colon Cancer: Gene >> CHN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222792
Start	29400583:29400583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751272925
CDS Mutation	c.331G>A
AA Mutation	p.Gly111Arg(p.G111R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222792
Start	29400818:29400818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375395261
CDS Mutation	c.566C>T
AA Mutation	p.Ala189Val(p.A189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222792
Start	29400566:29400566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314A>G
AA Mutation	p.Tyr105Cys(p.Y105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222792
Start	29496029:29496029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222792
Start	29512640:29512640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1316delC
AA Mutation	p.Pro439LeufsTer6(p.P439Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000222792
Start	29480278:29480278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CHN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222792
Start	29504809:29504809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>A
AA Mutation	p.Ala327Thr(p.A327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222792
Start	29507293:29507293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057A>C
AA Mutation	p.Lys353Gln(p.K353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript