Colon Cancer: Gene >> GLB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33046164:33046164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>A
AA Mutation	p.Asp342Asn(p.D342N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33072644:33072644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72555358
CDS Mutation	c.145C>T
AA Mutation	p.Arg49Cys(p.R49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33072554:33072554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553660803
CDS Mutation	c.235G>A
AA Mutation	p.Ala79Thr(p.A79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33097076:33097076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10T>C
AA Mutation	p.Phe4Leu(p.F4L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33058200:33058200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72555366
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33021634:33021634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165C>A
AA Mutation	p.Leu389Met(p.L389M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33058221:33058221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601C>G
AA Mutation	p.Arg201Gly(p.R201G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33051938:33051938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748853764
CDS Mutation	c.859G>A
AA Mutation	p.Glu287Lys(p.E287K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33021645:33021645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154T>C
AA Mutation	p.Val385Ala(p.V385A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307363
Start	33072687:33072687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307363
Start	33016745:33016745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000307363
Start	33072543:33072543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778423653
CDS Mutation	c.245+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GLB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	33058147:33058147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675A>C
AA Mutation	p.Lys225Asn(p.K225N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307363
Start	32997227:32997227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852G>A
AA Mutation	p.Val618Met(p.V618M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000307363
Start	33068899:33068900(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.316_317insGGTCTGTCCATGTGCAAA
AA Mutation	p.Tyr106delinsTrpSerValHisValGlnAsn(p.Y106delinsWSVHVQN)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript