Colon Cancer: Gene >> ADA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372874
Start	44625606:44625606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441G>T
AA Mutation	p.Lys147Asn(p.K147N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372874
Start	44636256:44636256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66C>G
AA Mutation	p.Ile22Met(p.I22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372874
Start	44622855:44622855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754C>A
AA Mutation	p.Leu252Met(p.L252M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372874
Start	44622609:44622609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824A>G
AA Mutation	p.Asp275Gly(p.D275G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372874
Start	44629095:44629095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170C>G
AA Mutation	p.Thr57Ser(p.T57S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372874
Start	44620322:44620322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055G>T
AA Mutation	p.Gly352Val(p.G352V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372874
Start	44624280:44624280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780518207
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372874
Start	44622589:44622589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559798694
CDS Mutation	c.844C>T
AA Mutation	p.Arg282Trp(p.R282W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript