Colon Cancer: Gene >> DCP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389063
Start	113013455:113013455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234A>G
AA Mutation	p.Asn412Asp(p.N412D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389063
Start	112976986:112976986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53G>T
AA Mutation	p.Ser18Ile(p.S18I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389063
Start	113001168:113001168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369278042
CDS Mutation	c.517C>T
AA Mutation	p.Arg173Cys(p.R173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389063
Start	113001206:113001206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555A>C
AA Mutation	p.Lys185Asn(p.K185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389063
Start	113001667:113001667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799A>G
AA Mutation	p.Lys267Glu(p.K267E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389063
Start	113010761:113010761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389063
Start	112985937:112985937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389063
Start	112976960:112976960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769592289
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000389063
Start	113001589:113001589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721C>T
AA Mutation	p.Arg241Ter(p.R241*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000389063
Start	113007937:113007937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DCP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389063
Start	113001454:113001454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683C>T
AA Mutation	p.Ala228Val(p.A228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389063
Start	113003944:113003944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748555203
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Gln(p.R270Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389063
Start	113007963:113007963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>A
AA Mutation	p.Arg323Lys(p.R323K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389063
Start	113013472:113013472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000389063
Start	113001147:113001147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Ter(p.R166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000389063
Start	113001590:113001592(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.724_726delAGA
AA Mutation	p.Arg242del(p.R242del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000389063
Start	113013340:113013342(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1119_1121delTAG
AA Mutation	p.Ser376del(p.S376del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript