Colon Cancer: Gene >> KDM4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6814685:6814685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375G>T
AA Mutation	p.Lys125Asn(p.K125N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6849543:6849543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472G>A
AA Mutation	p.Val158Ile(p.V158I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381309
Start	7103868:7103868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767764034
CDS Mutation	c.2608G>A
AA Mutation	p.Val870Met(p.V870M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7046905:7046905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776521442
CDS Mutation	c.2303C>T
AA Mutation	p.Thr768Met(p.T768M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7174665:7174665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3107C>T
AA Mutation	p.Ala1036Val(p.A1036V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6893122:6893122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811A>T
AA Mutation	p.Ile271Phe(p.I271F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6990453:6990453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774865352
CDS Mutation	c.1715G>A
AA Mutation	p.Arg572His(p.R572H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6984198:6984198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>A
AA Mutation	p.Pro383His(p.P383H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7013990:7013990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554533128
CDS Mutation	c.2171G>A
AA Mutation	p.Arg724Gln(p.R724Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	6986381:6986381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1392A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381309
Start	6849566:6849566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000381309
Start	6880040:6880040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779861232
CDS Mutation	c.658C>T
AA Mutation	p.Arg220Ter(p.R220*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KDM4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7013989:7013989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776351428
CDS Mutation	c.2170C>T
AA Mutation	p.Arg724Trp(p.R724W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	6880041:6880041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381309
Start	7013848:7013848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767131404
CDS Mutation	c.2029A>G
AA Mutation	p.Thr677Ala(p.T677A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000381309
Start	7011771:7011772(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1860_1861insCCCTTGAAGTGACGTTGGGCTAATAATCATCC
AA Mutation	p.Trp621ProfsTer4(p.W621Pfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript