Colon Cancer: Gene >> BAG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119676844:119676844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290G>T
AA Mutation	p.Glu430Asp(p.E430D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119672627:119672627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144585878
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Cys(p.R294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119651682:119651682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119670049:119670049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119651686:119651686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11C>T
AA Mutation	p.Ala4Val(p.A4V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119670032:119670032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369085
Start	119676922:119676922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369085
Start	119677084:119677084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369085
Start	119669928:119669928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369085
Start	119651742:119651742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.72delC
AA Mutation	p.Gly25AspfsTer186(p.G25Dfs*186)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BAG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369085
Start	119677172:119677172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1618G>A
AA Mutation	p.Gly540Arg(p.G540R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript