Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RALB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120278734:120278734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70G>T
AA Mutation	p.Gly24Cys(p.G24C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120278756:120278756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92C>T
AA Mutation	p.Thr31Met(p.T31M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120286075:120286075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139389446
CDS Mutation	c.316G>A
AA Mutation	p.Glu106Lys(p.E106K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272519
Start	120286035:120286035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RALB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120293162:120293162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>A
AA Mutation	p.Glu175Lys(p.E175K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120289588:120289588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745653359
CDS Mutation	c.332T>C
AA Mutation	p.Ile111Thr(p.I111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120293227:120293227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588G>T
AA Mutation	p.Lys196Asn(p.K196N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272519
Start	120286075:120286075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139389446
CDS Mutation	c.316G>A
AA Mutation	p.Glu106Lys(p.E106K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript