Colon Cancer: Gene >> STEAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393106
Start	119247805:119247805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748187004
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Cys(p.R207C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393106
Start	119248163:119248163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184644411
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393106
Start	119247754:119247754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201076547
CDS Mutation	c.568G>A
AA Mutation	p.Val190Met(p.V190M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119248119:119248119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119248159:119248159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119263296:119263296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1425G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119248012:119248012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.826C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119245571:119245571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119245604:119245604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764890933
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119254842:119254842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393106
Start	119263245:119263245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1374C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393106
Start	119245579:119245579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.87delC
AA Mutation	p.Val31TrpfsTer44(p.V31Wfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STEAP3

No Mutation Annotation!