Colon Cancer: Gene >> STEAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287908
Start	90227226:90227226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748A>C
AA Mutation	p.Ile250Leu(p.I250L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287908
Start	90229957:90229957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106G>A
AA Mutation	p.Gly369Asp(p.G369D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287908
Start	90225462:90225462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380A>G
AA Mutation	p.Glu127Gly(p.E127G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287908
Start	90225225:90225225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775060636
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287908
Start	90225187:90225187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287908
Start	90225136:90225136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000287908
Start	90229931:90229931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080T>G
AA Mutation	p.Tyr360Ter(p.Y360*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000287908
Start	90230019:90230019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772324565
CDS Mutation	c.1168G>T
AA Mutation	p.Glu390Ter(p.E390*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STEAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287908
Start	90225353:90225353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271G>T
AA Mutation	p.Val91Phe(p.V91F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000287908
Start	90225368:90225368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>T
AA Mutation	p.Glu96Ter(p.E96*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript