Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RIC8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526104
Start	209760:209760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486C>A
AA Mutation	p.Phe162Leu(p.F162L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526104
Start	211311:211311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751745965
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000526104
Start	212947:212947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321A>G
AA Mutation	p.Thr441Ala(p.T441A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526104
Start	212728:212728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526104
Start	209848:209848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762479589
CDS Mutation	c.574C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526104
Start	209625:209625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RIC8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526104
Start	214322:214322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568C>T
AA Mutation	p.Ser523Phe(p.S523F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526104
Start	209870:209870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596C>T
AA Mutation	p.Thr199Met(p.T199M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000526104
Start	209294:209294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108T>G
AA Mutation	p.Asp36Glu(p.D36E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript