Colon Cancer: Gene >> MVP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29835752:29835752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.626T>A
AA Mutation	p.Phe209Tyr(p.F209Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29844605:29844605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763449040
CDS Mutation	c.1747G>A
AA Mutation	p.Val583Met(p.V583M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29841928:29841928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1450C>T
AA Mutation	p.Pro484Ser(p.P484S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29830997:29830997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142974213
CDS Mutation	c.245G>A
AA Mutation	p.Arg82Gln(p.R82Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29834024:29834024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746050112
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Cys(p.R179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29844653:29844653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1795A>G
AA Mutation	p.Ile599Val(p.I599V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29847231:29847231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2300A>C
AA Mutation	p.Glu767Ala(p.E767A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29830910:29830910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158T>C
AA Mutation	p.Val53Ala(p.V53A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29841770:29841770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114581451
CDS Mutation	c.1366C>T
AA Mutation	p.Arg456Cys(p.R456C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357402
Start	29844656:29844656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779418542
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Cys(p.R600C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357402
Start	29844685:29844685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113018337
CDS Mutation	c.1827G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357402
Start	29833846:29833846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777830582
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357402
Start	29846239:29846239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761767691
CDS Mutation	c.2220C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357402
Start	29833762:29833762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357402
Start	29846197:29846197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139422591
CDS Mutation	c.2178C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357402
Start	29833995:29833995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.507delG
AA Mutation	p.Arg169SerfsTer23(p.R169Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357402
Start	29830911:29830911(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.164delC
AA Mutation	p.Pro55HisfsTer69(p.P55Hfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000357402
Start	29840289:29840289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021G>T
AA Mutation	p.Glu341Ter(p.E341*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MVP

No Mutation Annotation!