Colon Cancer: Gene >> GALR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329003
Start	76076808:76076808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329003
Start	76076914:76076914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647G>A
AA Mutation	p.Arg216His(p.R216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329003
Start	76077088:76077088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821G>A
AA Mutation	p.Arg274His(p.R274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329003
Start	76077087:76077087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Cys(p.R274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329003
Start	76075051:76075051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GALR2

No Mutation Annotation!