Colon Cancer: Gene >> RCC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373832
Start	28535369:28535369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528320406
CDS Mutation	c.650G>A
AA Mutation	p.Arg217Gln(p.R217Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373832
Start	28536767:28536767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Trp(p.R320W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373832
Start	28537834:28537834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760969624
CDS Mutation	c.1093C>T
AA Mutation	p.Arg365Cys(p.R365C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373832
Start	28532233:28532233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373832
Start	28536847:28536847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373832
Start	28531858:28531858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373832
Start	28529898:28529898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.38delC
AA Mutation	p.Pro13GlnfsTer11(p.P13Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RCC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373832
Start	28535087:28535087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479A>G
AA Mutation	p.Lys160Arg(p.K160R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373832
Start	28536376:28536376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745611564
CDS Mutation	c.932C>T
AA Mutation	p.Ser311Leu(p.S311L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript