Colon Cancer: Gene >> RS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18644615:18644615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61752145
CDS Mutation	c.337C>T
AA Mutation	p.Leu113Phe(p.L113F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18644530:18644530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61752159
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18647239:18647239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278A>G
AA Mutation	p.Tyr93Cys(p.Y93C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18642107:18642107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Arg191Gln(p.R191Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18642025:18642025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654G>C
AA Mutation	p.Glu218Asp(p.E218D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379984
Start	18672030:18672030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379984
Start	18656717:18656717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379984
Start	18657649:18657649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768728087
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379984
Start	18642094:18642094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18642041:18642041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs281865364
CDS Mutation	c.638G>A
AA Mutation	p.Arg213Gln(p.R213Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379984
Start	18656695:18656695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>A
AA Mutation	p.Ala48Thr(p.A48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript