Colon Cancer: Gene >> AICDA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8604812:8604812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>A
AA Mutation	p.Leu180Ile(p.L180I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8605429:8605429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213C>A
AA Mutation	p.Asp71Glu(p.D71E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8606966:8606966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Cys(p.R19C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8605248:8605248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394G>A
AA Mutation	p.Ala132Thr(p.A132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8606915:8606915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200228627
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Cys(p.R36C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8605281:8605281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Ala121Thr(p.A121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8604880:8604880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470G>T
AA Mutation	p.Arg157Ile(p.R157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8604821:8604821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Trp(p.R177W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229335
Start	8605411:8605411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754343795
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229335
Start	8605444:8605444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AICDA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8604914:8604914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436T>C
AA Mutation	p.Tyr146His(p.Y146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229335
Start	8605310:8605310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript