Colon Cancer: Gene >> STEAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297205
Start	90164562:90164562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848T>G
AA Mutation	p.Phe283Cys(p.F283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297205
Start	90159831:90159831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43A>G
AA Mutation	p.Lys15Glu(p.K15E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297205
Start	90161944:90161944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628G>A
AA Mutation	p.Glu210Lys(p.E210K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297205
Start	90164635:90164635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921A>G
AA Mutation	p.Ile307Met(p.I307M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297205
Start	90161251:90161251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531T>G
AA Mutation	p.Ile177Met(p.I177M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000297205
Start	90161276:90161276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779678323
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Ter(p.R186*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STEAP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297205
Start	90161086:90161086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297205
Start	90161053:90161053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333C>A
Mutation Classification	Silent
Feature Type	Transcript