Colon Cancer: Gene >> CYP17A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102837322:102837322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40T>C
AA Mutation	p.Tyr14His(p.Y14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102832610:102832610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61754278
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102830743:102830743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486C>T
AA Mutation	p.Arg496Cys(p.R496C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102834849:102834849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602A>G
AA Mutation	p.Tyr201Cys(p.Y201C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102830884:102830884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371825363
CDS Mutation	c.1345C>T
AA Mutation	p.Arg449Cys(p.R449C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102835332:102835332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358C>T
AA Mutation	p.His120Tyr(p.H120Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369887
Start	102835316:102835316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894154
CDS Mutation	c.374G>A
AA Mutation	p.Arg125Gln(p.R125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369887
Start	102833125:102833125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369887
Start	102833053:102833053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563749393
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369887
Start	102833065:102833065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369887
Start	102835306:102835306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369887
Start	102837251:102837251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000369887
Start	102833118:102833118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844C>T
AA Mutation	p.Gln282Ter(p.Q282*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000369887
Start	102831612:102831612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CYP17A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369887
Start	102830924:102830924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535705005
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript