Colon Cancer: Gene >> VTCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369458
Start	117156649:117156649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>T
AA Mutation	p.Asp124Tyr(p.D124Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369458
Start	117147779:117147779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775074986
CDS Mutation	c.728C>T
AA Mutation	p.Ser243Leu(p.S243L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369458
Start	117153280:117153280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535G>T
AA Mutation	p.Val179Leu(p.V179L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369458
Start	117156673:117156673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773228516
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Trp(p.R116W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369458
Start	117156774:117156774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245A>C
AA Mutation	p.Glu82Ala(p.E82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369458
Start	117156800:117156800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749882171
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369458
Start	117153263:117153263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VTCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369458
Start	117153242:117153242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573C>A
AA Mutation	p.Phe191Leu(p.F191L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript