Colon Cancer: Gene >> CYTH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427476
Start	48470617:48470617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368161948
CDS Mutation	c.182G>A
AA Mutation	p.Arg61Gln(p.R61Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000427476
Start	48470437:48470437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>A
AA Mutation	p.Arg35His(p.R35H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000427476
Start	48473314:48473314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427476
Start	48469516:48469516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYTH2

No Mutation Annotation!