Colon Cancer: Gene >> YBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321358
Start	42696711:42696711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321358
Start	42700912:42700912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872G>A
AA Mutation	p.Arg291His(p.R291H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321358
Start	42683429:42683429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193T>G
AA Mutation	p.Trp65Gly(p.W65G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321358
Start	42700978:42700978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141968223
CDS Mutation	c.938C>T
AA Mutation	p.Ser313Leu(p.S313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321358
Start	42696727:42696727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440G>A
AA Mutation	p.Arg147His(p.R147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321358
Start	42697185:42697185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> YBX1

No Mutation Annotation!