Colon Cancer: Gene >> STEAP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282981:88282981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644T>C
AA Mutation	p.Phe215Ser(p.F215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88283086:88283086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539A>G
AA Mutation	p.Gln180Arg(p.Q180R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88279574:88279574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781764701
CDS Mutation	c.1204G>A
AA Mutation	p.Gly402Ser(p.G402S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282714:88282714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911A>G
AA Mutation	p.His304Arg(p.H304R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88284121:88284121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750091751
CDS Mutation	c.149G>A
AA Mutation	p.Arg50Gln(p.R50Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282684:88282684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368689133
CDS Mutation	c.941G>A
AA Mutation	p.Arg314Gln(p.R314Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282916:88282916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769390918
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88283965:88283965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>C
AA Mutation	p.Val102Ala(p.V102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380079
Start	88279487:88279487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380079
Start	88282959:88282959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370475892
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000380079
Start	88283999:88283999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>T
AA Mutation	p.Glu91Ter(p.E91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STEAP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88280967:88280967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097C>A
AA Mutation	p.Ser366Tyr(p.S366Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282916:88282916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769390918
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88283060:88283060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565A>G
AA Mutation	p.Ile189Val(p.I189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282951:88282951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674A>G
AA Mutation	p.Tyr225Cys(p.Y225C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282756:88282756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377052757
CDS Mutation	c.869G>A
AA Mutation	p.Arg290Gln(p.R290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380079
Start	88282977:88282977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648C>A
AA Mutation	p.Phe216Leu(p.F216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript