Colon Cancer: Gene >> BEND5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48759118:48759118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527C>A
AA Mutation	p.Ala176Asp(p.A176D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48759164:48759164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374150750
CDS Mutation	c.481G>A
AA Mutation	p.Val161Met(p.V161M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48759053:48759053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201098567
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48728001:48728001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1151C>G
AA Mutation	p.Thr384Ser(p.T384S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48742685:48742685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832A>G
AA Mutation	p.Thr278Ala(p.T278A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48742699:48742699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818G>A
AA Mutation	p.Ser273Asn(p.S273N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48727998:48727998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154A>C
AA Mutation	p.Glu385Ala(p.E385A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48727895:48727895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257T>A
AA Mutation	p.Asn419Lys(p.N419K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48727993:48727993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159G>A
AA Mutation	p.Ala387Thr(p.A387T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371833
Start	48728015:48728015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BEND5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48759053:48759053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201098567
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371833
Start	48759052:48759052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756507130
CDS Mutation	c.593G>A
AA Mutation	p.Arg198His(p.R198H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371833
Start	48727949:48727949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203C>A
Mutation Classification	Silent
Feature Type	Transcript