Colon Cancer: Gene >> KDM4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43691013:43691013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757083813
CDS Mutation	c.2206G>A
AA Mutation	p.Val736Ile(p.V736I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43694838:43694838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2614G>A
AA Mutation	p.Asp872Asn(p.D872N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43671634:43671634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369667794
CDS Mutation	c.1493G>A
AA Mutation	p.Arg498His(p.R498H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43689027:43689027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1969T>G
AA Mutation	p.Phe657Val(p.F657V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43666458:43666458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680T>C
AA Mutation	p.Phe227Ser(p.F227S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43683692:43683692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1743T>G
AA Mutation	p.Asp581Glu(p.D581E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43653179:43653179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43667818:43667818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962T>C
AA Mutation	p.Val321Ala(p.V321A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43660335:43660335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352G>A
AA Mutation	p.Glu118Lys(p.E118K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43666972:43666972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796G>A
AA Mutation	p.Glu266Lys(p.E266K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43655609:43655609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157T>G
AA Mutation	p.Trp53Gly(p.W53G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43660339:43660339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769652752
CDS Mutation	c.356G>A
AA Mutation	p.Arg119Gln(p.R119Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43671840:43671840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190275733
CDS Mutation	c.1699G>A
AA Mutation	p.Ala567Thr(p.A567T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372396
Start	43704262:43704262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372396
Start	43697905:43697905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779996010
CDS Mutation	c.2733C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372396
Start	43697950:43697950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761299911
CDS Mutation	c.2778C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000372396
Start	43666454:43666454(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.680delT
AA Mutation	p.Phe227SerfsTer16(p.F227Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372396
Start	43690902:43690902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2096delA
AA Mutation	p.Lys699SerfsTer7(p.K699Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000372396
Start	43694104:43694104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2484+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000372396
Start	43692291:43692293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2356_2358delCAG
AA Mutation	p.Gln786del(p.Q786del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KDM4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372396
Start	43704096:43704096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3038G>T
AA Mutation	p.Arg1013Ile(p.R1013I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372396
Start	43663022:43663022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000372396
Start	43662893:43662893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript