Colon Cancer: Gene >> VGF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249330
Start	101163708:101163708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532601632
CDS Mutation	c.1136G>T
AA Mutation	p.Gly379Val(p.G379V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249330
Start	101163507:101163507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337A>G
AA Mutation	p.Glu446Gly(p.E446G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249330
Start	101163739:101163739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105C>G
AA Mutation	p.Gln369Glu(p.Q369E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249330
Start	101164816:101164816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28G>A
AA Mutation	p.Ala10Thr(p.A10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249330
Start	101163515:101163515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329C>G
AA Mutation	p.Asp443Glu(p.D443E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VGF

No Mutation Annotation!