Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RND3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263895
Start	150474981:150474981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242C>A
AA Mutation	p.Ser81Tyr(p.S81Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263895
Start	150470148:150470148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765035010
CDS Mutation	c.574G>A
AA Mutation	p.Val192Ile(p.V192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263895
Start	150486704:150486704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228G>T
AA Mutation	p.Trp76Cys(p.W76C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RND3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263895
Start	150474933:150474933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>T
AA Mutation	p.Ala97Val(p.A97V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263895
Start	150474939:150474939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747141041
CDS Mutation	c.284C>T
AA Mutation	p.Ser95Leu(p.S95L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript