Colon Cancer: Gene >> DNAJC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65392598:65392598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465G>A
AA Mutation	p.Ala489Thr(p.A489T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65405937:65405937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124C>A
AA Mutation	p.Ser708Arg(p.S708R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65405951:65405951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762235583
CDS Mutation	c.2138C>T
AA Mutation	p.Ala713Val(p.A713V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65392677:65392677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141779215
CDS Mutation	c.1544C>T
AA Mutation	p.Ala515Val(p.A515V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65385756:65385756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368061386
CDS Mutation	c.674G>A
AA Mutation	p.Arg225His(p.R225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65385836:65385836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Cys(p.R252C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65412951:65412951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755391548
CDS Mutation	c.2668G>A
AA Mutation	p.Ala890Thr(p.A890T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65264917:65264917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369238276
CDS Mutation	c.7G>T
AA Mutation	p.Asp3Tyr(p.D3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65392819:65392819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1686C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65411315:65411315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65385778:65385778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754216239
CDS Mutation	c.696A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65389569:65389569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65379488:65379488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395325
Start	65408709:65408709(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2393delA
AA Mutation	p.Lys798ArgfsTer6(p.K798Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000395325
Start	65365884:65365884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65366153:65366153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329A>C
AA Mutation	p.Asn110Thr(p.N110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65385900:65385900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375848137
CDS Mutation	c.818G>A
AA Mutation	p.Arg273Gln(p.R273Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395325
Start	65401805:65401805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762410856
CDS Mutation	c.1981G>A
AA Mutation	p.Gly661Arg(p.G661R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65395019:65395019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185245369
CDS Mutation	c.1854G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65411361:65411361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2575C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65392678:65392678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201766287
CDS Mutation	c.1545G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395325
Start	65389394:65389394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000395325
Start	65384292:65384292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Ter(p.R199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript