Colon Cancer: Gene >> DBNDD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372720
Start	45408421:45408421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248G>A
AA Mutation	p.Arg83Gln(p.R83Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372720
Start	45408833:45408833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466A>C
AA Mutation	p.Asn156His(p.N156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372720
Start	45408606:45408606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772958543
CDS Mutation	c.433C>T
AA Mutation	p.Pro145Ser(p.P145S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372720
Start	45408387:45408387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767159514
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372720
Start	45410034:45410034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674T>C
AA Mutation	p.Leu225Pro(p.L225P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DBNDD2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372720
Start	45408404:45408404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript