Colon Cancer: Gene >> HRAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311189
Start	533499:533499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404G>A
AA Mutation	p.Arg135Gln(p.R135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311189
Start	533878:533878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Gly60Ser(p.G60S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311189
Start	532700:532700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142218590
CDS Mutation	c.506G>A
AA Mutation	p.Arg169Gln(p.R169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311189
Start	533573:533573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200747280
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311189
Start	533834:533834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372223975
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HRAS

No Mutation Annotation!