Colon Cancer: Gene >> BAG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287322
Start	38210119:38210119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000C>A
AA Mutation	p.Leu334Ile(p.L334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287322
Start	38210364:38210364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245G>A
AA Mutation	p.Met415Ile(p.M415I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287322
Start	38176917:38176917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287322
Start	38210477:38210477(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1365delA
AA Mutation	p.Gly456AspfsTer6(p.G456Dfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000287322
Start	38210314:38210314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>T
AA Mutation	p.Glu399Ter(p.E399*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287322
Start	38210476:38210477(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1365dupA
AA Mutation	p.Gly456ArgfsTer70(p.G456Rfs*70)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BAG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287322
Start	38192763:38192763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346A>G
AA Mutation	p.Thr116Ala(p.T116A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript