Colon Cancer: Gene >> COMMD10

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000274458
Start	116291576:116291576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>T
AA Mutation	p.Lys190Asn(p.K190N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274458
Start	116134119:116134119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274458
Start	116091152:116091152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206A>G
AA Mutation	p.His69Arg(p.H69R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274458
Start	116292486:116292486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274458
Start	116092604:116092605(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.303_304insCATACTG
AA Mutation	p.Arg102HisfsTer8(p.R102Hfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> COMMD10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274458
Start	116092623:116092623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>T
AA Mutation	p.Ala108Ser(p.A108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript