Colon Cancer: Gene >> RPS6KB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225577
Start	59946612:59946612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1402C>A
AA Mutation	p.Pro468Thr(p.P468T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225577
Start	59946690:59946690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1480G>A
AA Mutation	p.Ala494Thr(p.A494T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225577
Start	59912775:59912775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Trp(p.R95W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225577
Start	59936475:59936475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053C>A
AA Mutation	p.Phe351Leu(p.F351L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225577
Start	59893322:59893322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.141+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000225577
Start	59934253:59934253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>T
AA Mutation	p.Glu258Ter(p.E258*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225577
Start	59946728:59946729(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1524dupA
AA Mutation	p.Gln509ThrfsTer24(p.Q509Tfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KB1

No Mutation Annotation!