Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ERVW-1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000493463
Start	92469958:92469958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424A>G
AA Mutation	p.Thr142Ala(p.T142A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000493463
Start	92469895:92469895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758687766
CDS Mutation	c.487C>T
AA Mutation	p.Arg163Cys(p.R163C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000493463
Start	92469591:92469591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791T>C
AA Mutation	p.Leu264Pro(p.L264P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000493463
Start	92470337:92470337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000493463
Start	92469692:92469692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000493463
Start	92469149:92469149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745829714
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000493463
Start	92470232:92470233(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs750124319
CDS Mutation	c.149dupC
AA Mutation	p.Ser51IlefsTer3(p.S51Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ERVW-1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000493463
Start	92470018:92470018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145102856
CDS Mutation	c.364G>T
AA Mutation	p.Asp122Tyr(p.D122Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000493463
Start	92468813:92468813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1569C>A
Mutation Classification	Silent
Feature Type	Transcript