Colon Cancer: Gene >> ACR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216139
Start	50744867:50744867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770629027
CDS Mutation	c.926C>T
AA Mutation	p.Pro309Leu(p.P309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216139
Start	50739764:50739764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352G>T
AA Mutation	p.Ala118Ser(p.A118S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216139
Start	50744154:50744154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659A>T
AA Mutation	p.Gln220Leu(p.Q220L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216139
Start	50738307:50738307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151269264
CDS Mutation	c.72G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216139
Start	50738301:50738301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368378183
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216139
Start	50744149:50744149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558788452
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216139
Start	50744736:50744736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000216139
Start	50744974:50744974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Ter(p.R345*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ACR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216139
Start	50744193:50744193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698T>C
AA Mutation	p.Ile233Thr(p.I233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216139
Start	50744108:50744108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>A
AA Mutation	p.Asp205Asn(p.D205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216139
Start	50739721:50739721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript