Colon Cancer: Gene >> CDS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000460006
Start	5185782:5185782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>T
AA Mutation	p.Gly262Cys(p.G262C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000460006
Start	5189778:5189778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761127363
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000460006
Start	5184910:5184910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724T>G
AA Mutation	p.Phe242Val(p.F242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000460006
Start	5176702:5176702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576280057
CDS Mutation	c.346G>A
AA Mutation	p.Val116Ile(p.V116I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000460006
Start	5190116:5190116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220G>T
AA Mutation	p.Ser407Ile(p.S407I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000460006
Start	5189825:5189825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192G>A
AA Mutation	p.Ala398Thr(p.A398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460006
Start	5186836:5186836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460006
Start	5176656:5176656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536071538
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000460006
Start	5189067:5189067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.985delA
AA Mutation	p.Thr329ArgfsTer60(p.T329Rfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDS2

No Mutation Annotation!