Colon Cancer: Gene >> HERPUD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439977
Start	56940226:56940226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886G>A
AA Mutation	p.Ala296Thr(p.A296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439977
Start	56940169:56940169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829T>G
AA Mutation	p.Phe277Val(p.F277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439977
Start	56935469:56935469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150953986
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439977
Start	56939252:56939252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439977
Start	56940194:56940194(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.855delC
AA Mutation	p.Ser286ProfsTer2(p.S286Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439977
Start	56935405:56935405(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.234delA
AA Mutation	p.Lys78AsnfsTer11(p.K78Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HERPUD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439977
Start	56936780:56936780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527424441
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Trp(p.R132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript