Colon Cancer: Gene >> HTRA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8302505:8302505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094C>T
AA Mutation	p.Thr365Ile(p.T365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8294163:8294163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>G
AA Mutation	p.Thr338Arg(p.T338R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8291497:8291497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836G>A
AA Mutation	p.Arg279Gln(p.R279Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8306086:8306086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137866031
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Trp(p.R438W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8291548:8291548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887C>T
AA Mutation	p.Thr296Met(p.T296M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8306050:8306050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>A
AA Mutation	p.Val426Met(p.V426M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8305999:8305999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225G>A
AA Mutation	p.Val409Ile(p.V409I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8282461:8282461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746960044
CDS Mutation	c.410G>A
AA Mutation	p.Arg137His(p.R137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307358
Start	8304262:8304262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145508993
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307358
Start	8306085:8306085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307358
Start	8292333:8292333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.920delG
AA Mutation	p.Gly307AspfsTer4(p.G307Dfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HTRA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307358
Start	8286597:8286597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522C>A
AA Mutation	p.Ser174Arg(p.S174R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307358
Start	8304262:8304262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145508993
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript