Colon Cancer: Gene >> CA12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000178638
Start	63345548:63345548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358C>A
AA Mutation	p.Leu120Met(p.L120M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000178638
Start	63345485:63345485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421G>A
AA Mutation	p.Ala141Thr(p.A141T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000178638
Start	63381696:63381696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25G>A
AA Mutation	p.Ala9Thr(p.A9T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000178638
Start	63327164:63327164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.977T>C
AA Mutation	p.Leu326Pro(p.L326P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000178638
Start	63342042:63342042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485A>G
AA Mutation	p.Asn162Ser(p.N162S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000178638
Start	63340767:63340767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542C>T
AA Mutation	p.Pro181Leu(p.P181L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000178638
Start	63345486:63345486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777028896
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CA12

No Mutation Annotation!