Colon Cancer: Gene >> RORA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60503547:60503547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063C>A
AA Mutation	p.Leu355Ile(p.L355I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60678674:60678674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188796486
CDS Mutation	c.179C>T
AA Mutation	p.Thr60Met(p.T60M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60511527:60511527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>C
AA Mutation	p.Gln173His(p.Q173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60514672:60514672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368A>G
AA Mutation	p.Asn123Ser(p.N123S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60497559:60497559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468G>T
AA Mutation	p.Ala490Ser(p.A490S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335670
Start	61229128:61229128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335670
Start	60511347:60511347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335670
Start	60511611:60511611(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.435delT
AA Mutation	p.Phe145LeufsTer38(p.F145Lfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000335670
Start	60514655:60514655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385C>T
AA Mutation	p.Arg129Ter(p.R129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RORA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60505602:60505602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848C>T
AA Mutation	p.Ser283Leu(p.S283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60511346:60511346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>A
AA Mutation	p.Leu234Ile(p.L234I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript