Colon Cancer: Gene >> GRWD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253237
Start	48446150:48446150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145A>G
AA Mutation	p.Met49Val(p.M49V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253237
Start	48451082:48451082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874C>T
AA Mutation	p.Arg292Trp(p.R292W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253237
Start	48450489:48450489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758598151
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253237
Start	48450736:48450736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766182030
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253237
Start	48452872:48452872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770406802
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253237
Start	48451078:48451078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777544717
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GRWD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253237
Start	48450357:48450357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513G>T
AA Mutation	p.Glu171Asp(p.E171D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript