Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334047
Start	94533160:94533160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>A
AA Mutation	p.Ser174Asn(p.S174N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334047
Start	94536150:94536150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227A>G
AA Mutation	p.Asp76Gly(p.D76G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334047
Start	94535973:94535973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404A>G
AA Mutation	p.Tyr135Cys(p.Y135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334047
Start	94535984:94535984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334047
Start	94533138:94533138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334047
Start	94533152:94533152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>T
AA Mutation	p.Asp177Tyr(p.D177Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334047
Start	94540342:94540342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127A>G
AA Mutation	p.Asn43Asp(p.N43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000334047
Start	94536049:94536051(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.326_328delCCT
AA Mutation	p.Ser109del(p.S109del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript