Colon Cancer: Gene >> AMFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290649
Start	56414274:56414274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326C>G
AA Mutation	p.Pro109Arg(p.P109R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290649
Start	56363966:56363966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1739G>A
AA Mutation	p.Arg580His(p.R580H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290649
Start	56369218:56369218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750744117
CDS Mutation	c.1490G>A
AA Mutation	p.Arg497Gln(p.R497Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290649
Start	56389233:56389233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770366707
CDS Mutation	c.1228G>A
AA Mutation	p.Glu410Lys(p.E410K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290649
Start	56389204:56389204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290649
Start	56408015:56408015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AMFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290649
Start	56409579:56409579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Asp120Tyr(p.D120Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290649
Start	56389189:56389189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747289090
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript