Colon Cancer: Gene >> BAG6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31641141:31641141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2660A>G
AA Mutation	p.Gln887Arg(p.Q887R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31644999:31644999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773367157
CDS Mutation	c.1334G>A
AA Mutation	p.Arg445Gln(p.R445Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31645072:31645072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>A
AA Mutation	p.Glu421Lys(p.E421K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31647673:31647673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Cys(p.R242C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31644125:31644125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1535C>A
AA Mutation	p.Ala512Asp(p.A512D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31640686:31640686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150422210
CDS Mutation	c.2863A>G
AA Mutation	p.Met955Val(p.M955V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375964
Start	31647623:31647623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375964
Start	31640232:31640232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3123C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375964
Start	31645193:31645193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1140T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375964
Start	31645064:31645064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375964
Start	31651661:31651661(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.103delG
AA Mutation	p.Ala35ProfsTer3(p.A35Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000375964
Start	31640794:31640794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2842delC
AA Mutation	p.Gln948SerfsTer85(p.Q948Sfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BAG6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31642163:31642163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2194C>T
AA Mutation	p.Arg732Cys(p.R732C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375964
Start	31642216:31642216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2141G>A
AA Mutation	p.Gly714Asp(p.G714D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375964
Start	31642255:31642256(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2101_2102insC
AA Mutation	p.Phe701SerfsTer24(p.F701Sfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript