Colon Cancer: Gene >> YES1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314574
Start	756804:756804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24A>C
AA Mutation	p.Glu8Asp(p.E8D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314574
Start	742951:742951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
AA Mutation	p.Pro343Ser(p.P343S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314574
Start	747987:747987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202083013
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314574
Start	736946:736946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153G>A
AA Mutation	p.Ala385Thr(p.A385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314574
Start	745788:745788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644G>T
AA Mutation	p.Arg215Met(p.R215M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314574
Start	756699:756699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533246934
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314574
Start	751800:751800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314574
Start	732952:732952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314574
Start	724568:724568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1488C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000314574
Start	756837:756837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773348637
CDS Mutation	c.-8-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> YES1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000314574
Start	724435:724435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>T
AA Mutation	p.Glu541Ter(p.E541*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript