Colon Cancer: Gene >> RHBDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341329
Start	226906809:226906809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.His195Tyr(p.H195Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341329
Start	226865117:226865117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>A
AA Mutation	p.Gly142Ser(p.G142S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341329
Start	226865054:226865054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
AA Mutation	p.Leu121Phe(p.L121F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341329
Start	226914317:226914317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138482669
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341329
Start	226914299:226914300(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.804_805insTTGTTTTATACTTCCTGTTTTGT
AA Mutation	p.Ser269LeufsTer44(p.S269Lfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RHBDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341329
Start	226914301:226914301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806G>A
AA Mutation	p.Ser269Asn(p.S269N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341329
Start	226864983:226864983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745642950
CDS Mutation	c.290G>T
AA Mutation	p.Arg97Ile(p.R97I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript