Colon Cancer: Gene >> DNAJA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262375
Start	4443047:4443047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753693250
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262375
Start	4448772:4448772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>A
AA Mutation	p.Gly389Ser(p.G389S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262375
Start	4444710:4444710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978A>C
AA Mutation	p.Glu326Asp(p.E326D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262375
Start	4448738:4448738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262375
Start	4434419:4434419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.248delT
AA Mutation	p.Phe83SerfsTer16(p.F83Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000262375
Start	4448735:4448735(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1133delC
AA Mutation	p.Pro378LeufsTer39(p.P378Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262375
Start	4442298:4442298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661G>A
AA Mutation	p.Ala221Thr(p.A221T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262375
Start	4441407:4441407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747841929
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript