Colon Cancer: Gene >> CALML3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315238
Start	5525143:5525143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.58T>A
AA Mutation	p.Phe20Ile(p.F20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315238
Start	5525304:5525304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>T
AA Mutation	p.Met73Ile(p.M73I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315238
Start	5525293:5525293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315238
Start	5525424:5525424(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.343delG
AA Mutation	p.Glu115ArgfsTer3(p.E115Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CALML3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315238
Start	5525219:5525219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134C>T
AA Mutation	p.Thr45Met(p.T45M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript