Colon Cancer: Gene >> DNAJC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182741246:182741246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760624957
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Cys(p.R361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182751766:182751766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415T>C
AA Mutation	p.Leu472Pro(p.L472P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182720158:182720158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776207150
CDS Mutation	c.356G>A
AA Mutation	p.Arg119His(p.R119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182762778:182762778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2242T>A
AA Mutation	p.Phe748Ile(p.F748I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182728960:182728960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599G>A
AA Mutation	p.Ser200Asn(p.S200N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182756389:182756389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371494397
CDS Mutation	c.1729G>A
AA Mutation	p.Glu577Lys(p.E577K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182756464:182756464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804G>A
AA Mutation	p.Ala602Thr(p.A602T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182756408:182756408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750671995
CDS Mutation	c.1748T>G
AA Mutation	p.Phe583Cys(p.F583C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182740372:182740372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201843743
CDS Mutation	c.1061C>T
AA Mutation	p.Ser354Leu(p.S354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182756350:182756350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1690A>G
AA Mutation	p.Thr564Ala(p.T564A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264065
Start	182755029:182755029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1578A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264065
Start	182756388:182756388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764733833
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264065
Start	182757788:182757788(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1911delT
AA Mutation	p.Pro639GlnfsTer22(p.P639Qfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264065
Start	182756449:182756449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789G>T
AA Mutation	p.Glu597Ter(p.E597*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000264065
Start	182728881:182728881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520G>T
AA Mutation	p.Glu174Ter(p.E174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264065
Start	182741286:182741287(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1127dupA
AA Mutation	p.Asn376LysfsTer2(p.N376Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264065
Start	182718250:182718251(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.164_165insATTTAAC
AA Mutation	p.Phe55LeufsTer13(p.F55Lfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182751776:182751776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1425C>A
AA Mutation	p.Phe475Leu(p.F475L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264065
Start	182762786:182762786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250C>A
AA Mutation	p.Phe750Leu(p.F750L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264065
Start	182722073:182722073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416T>G
AA Mutation	p.Phe139Cys(p.F139C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript