Colon Cancer: Gene >> ACVR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157778241:157778241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157766118:157766118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869C>T
AA Mutation	p.Ser290Leu(p.S290L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157780426:157780426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242G>A
AA Mutation	p.Cys81Tyr(p.C81Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157737650:157737650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411G>T
AA Mutation	p.Ala471Ser(p.A471S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157766092:157766092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895A>G
AA Mutation	p.Thr299Ala(p.T299A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157761021:157761021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751000395
CDS Mutation	c.1123C>T
AA Mutation	p.Arg375Cys(p.R375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157774183:157774183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548T>C
AA Mutation	p.Leu183Ser(p.L183S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263640
Start	157770411:157770411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775087563
CDS Mutation	c.747G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACVR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157770477:157770477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>T
AA Mutation	p.Trp227Cys(p.W227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263640
Start	157766118:157766118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869C>T
AA Mutation	p.Ser290Leu(p.S290L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript