Colon Cancer: Gene >> C1D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355848
Start	68043049:68043049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266G>T
AA Mutation	p.Arg89Ile(p.R89I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355848
Start	68047304:68047304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Gly3Ser(p.G3S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355848
Start	68047279:68047279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32C>T
AA Mutation	p.Pro11Leu(p.P11L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355848
Start	68047202:68047202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109T>C
AA Mutation	p.Ser37Pro(p.S37P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355848
Start	68046347:68046347(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.202delT
AA Mutation	p.Trp68GlyfsTer16(p.W68Gfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000355848
Start	68047298:68047298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13G>T
AA Mutation	p.Glu5Ter(p.E5*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> C1D

Mutation ID	1
Mutation Consequence	start_lost
Transcription ID	ENST00000355848
Start	68047310:68047310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1A>T
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript