Colon Cancer: Gene >> BEND4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42117649:42117649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751788865
CDS Mutation	c.1474G>A
AA Mutation	p.Gly492Ser(p.G492S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42152028:42152028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116A>T
AA Mutation	p.Lys39Met(p.K39M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42143486:42143486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996G>T
AA Mutation	p.Glu332Asp(p.E332D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42143757:42143757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725C>T
AA Mutation	p.Thr242Ile(p.T242I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42125660:42125660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759165820
CDS Mutation	c.1069G>A
AA Mutation	p.Val357Ile(p.V357I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42125599:42125599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130C>A
AA Mutation	p.Ala377Asp(p.A377D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42143967:42143967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515C>T
AA Mutation	p.Ala172Val(p.A172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42143584:42143584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898G>A
AA Mutation	p.Glu300Lys(p.E300K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502486
Start	42120145:42120145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502486
Start	42143504:42143504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502486
Start	42143660:42143660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000502486
Start	42151880:42151880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.264delC
AA Mutation	p.Gly91AlafsTer23(p.G91Afs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BEND4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42143747:42143747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735T>G
AA Mutation	p.Phe245Leu(p.F245L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502486
Start	42143941:42143941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541C>A
AA Mutation	p.Leu181Ile(p.L181I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502486
Start	42117680:42117680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1443G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502486
Start	42143855:42143855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574971489
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript