Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DNMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10140094:10140094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3710C>T
AA Mutation	p.Ser1237Leu(p.S1237L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10156448:10156448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751093624
CDS Mutation	c.1294G>A
AA Mutation	p.Glu432Lys(p.E432K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10154638:10154638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1732A>G
AA Mutation	p.Thr578Ala(p.T578A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10175574:10175574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781646588
CDS Mutation	c.566C>T
AA Mutation	p.Ser189Leu(p.S189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10154710:10154710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1660G>C
AA Mutation	p.Ala554Pro(p.A554P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10154910:10154910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591A>G
AA Mutation	p.Ile531Val(p.I531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10154710:10154710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1660G>A
AA Mutation	p.Ala554Thr(p.A554T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10142113:10142113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779489678
CDS Mutation	c.3176G>A
AA Mutation	p.Arg1059His(p.R1059H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10156453:10156453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289A>G
AA Mutation	p.Asn430Ser(p.N430S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10175577:10175577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563A>C
AA Mutation	p.Lys188Thr(p.K188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10143961:10143961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958His(p.R958H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10135740:10135740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4721G>A
AA Mutation	p.Arg1574Gln(p.R1574Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10162737:10162737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775360871
CDS Mutation	c.890G>A
AA Mutation	p.Arg297Gln(p.R297Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10143959:10143959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2875C>T
AA Mutation	p.Pro959Ser(p.P959S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10180384:10180384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369311643
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10154371:10154371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10148937:10148937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199832007
CDS Mutation	c.2619C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10140141:10140141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139909192
CDS Mutation	c.3663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10137931:10137931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4146G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10162670:10162670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10166634:10166634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755151805
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10142052:10142052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10148982:10148982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375136816
CDS Mutation	c.2574C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10140276:10140276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772752543
CDS Mutation	c.3528G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10151512:10151512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10173123:10173123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340748
Start	10160050:10160050(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1009delA
AA Mutation	p.Met337TrpfsTer8(p.M337Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000340748
Start	10182046:10182046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>T
AA Mutation	p.Glu38Ter(p.E38*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DNMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10137980:10137980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4097C>T
AA Mutation	p.Thr1366Met(p.T1366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10156448:10156448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751093624
CDS Mutation	c.1294G>A
AA Mutation	p.Glu432Lys(p.E432K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10166606:10166606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.835G>A
AA Mutation	p.Asp279Asn(p.D279N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10155048:10155048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453G>A
AA Mutation	p.Glu485Lys(p.E485K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10173121:10173121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771381056
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10143961:10143961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958His(p.R958H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340748
Start	10173131:10173131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679T>G
AA Mutation	p.Ser227Ala(p.S227A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10140132:10140132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3672G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340748
Start	10151422:10151422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2193C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340748
Start	10180861:10180862(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.141_142insG
AA Mutation	p.Leu48AlafsTer16(p.L48Afs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript