Colon Cancer: Gene >> VDR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229022
Start	47865124:47865124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753383761
CDS Mutation	c.200G>A
AA Mutation	p.Arg67His(p.R67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229022
Start	47844936:47844936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762188448
CDS Mutation	c.1094C>T
AA Mutation	p.Thr365Met(p.T365M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229022
Start	47846790:47846790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>A
AA Mutation	p.Asp258Glu(p.D258E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229022
Start	47846708:47846708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856T>C
AA Mutation	p.Trp286Arg(p.W286R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229022
Start	47857220:47857220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229022
Start	47844908:47844908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368961482
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229022
Start	47865090:47865090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229022
Start	47844773:47844773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550308645
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VDR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229022
Start	47844825:47844825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205G>A
AA Mutation	p.Arg402His(p.R402H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript