Colon Cancer: Gene >> MR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367580
Start	181049121:181049121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775161220
CDS Mutation	c.137C>T
AA Mutation	p.Ser46Leu(p.S46L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367580
Start	181050086:181050086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367580
Start	181049285:181049285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763132197
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Cys(p.R101C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367580
Start	181052446:181052446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377066166
CDS Mutation	c.816C>A
AA Mutation	p.Ser272Arg(p.S272R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367580
Start	181052301:181052301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367580
Start	181052479:181052479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751845229
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367580
Start	181053583:181053583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367580
Start	181052314:181052314(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.689delC
AA Mutation	p.Pro230GlnfsTer5(p.P230Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MR1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367580
Start	181052510:181052510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>C
AA Mutation	p.Glu294Gln(p.E294Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367580
Start	181052353:181052353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723A>C
AA Mutation	p.Glu241Asp(p.E241D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript