Colon Cancer: Gene >> DNAJC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376980
Start	21920832:21920832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503C>T
AA Mutation	p.Ala168Val(p.A168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376980
Start	21806023:21806023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747599230
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352Gln(p.R352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376980
Start	21759327:21759327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439G>T
AA Mutation	p.Ser480Ile(p.S480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376980
Start	21928545:21928545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376980
Start	21759518:21759518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781405082
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376980
Start	21806004:21806004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574582224
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376980
Start	21759467:21759467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376980
Start	21882285:21882285(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.975delA
AA Mutation	p.Lys325AsnfsTer14(p.K325Nfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376980
Start	21882284:21882285(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.975dupA
AA Mutation	p.Gln326ThrfsTer4(p.Q326Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376980
Start	21759507:21759508(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1258dupG
AA Mutation	p.Val420GlyfsTer13(p.V420Gfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376980
Start	21928532:21928532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345T>G
Mutation Classification	Silent
Feature Type	Transcript