Colon Cancer: Gene >> RWDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000466444
Start	116588968:116588968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000466444
Start	116590320:116590320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463A>G
AA Mutation	p.Lys155Glu(p.K155E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000466444
Start	116580342:116580342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121G>A
AA Mutation	p.Ala41Thr(p.A41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000466444
Start	116588949:116588949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>T
AA Mutation	p.Lys126Asn(p.K126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RWDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000466444
Start	116588949:116588949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>T
AA Mutation	p.Lys126Asn(p.K126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000466444
Start	116590902:116590902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562G>T
AA Mutation	p.Glu188Ter(p.E188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript