Colon Cancer: Gene >> DHDDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236342
Start	26446350:26446350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358G>A
AA Mutation	p.Val120Ile(p.V120I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000236342
Start	26438244:26438244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149949619
CDS Mutation	c.140G>A
AA Mutation	p.Arg47Gln(p.R47Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000236342
Start	26447621:26447621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503A>T
AA Mutation	p.Glu168Val(p.E168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000236342
Start	26442804:26442804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254G>A
AA Mutation	p.Arg85His(p.R85H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236342
Start	26447630:26447630(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.517delG
AA Mutation	p.Val173TrpfsTer31(p.V173Wfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DHDDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236342
Start	26460103:26460103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>A
AA Mutation	p.Glu242Lys(p.E242K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236342
Start	26438209:26438209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>T
Mutation Classification	Silent
Feature Type	Transcript