Colon Cancer: Gene >> DNMT3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32784827:32784827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149520896
CDS Mutation	c.274C>T
AA Mutation	p.Arg92Trp(p.R92W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32807818:32807818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2477G>A
AA Mutation	p.Arg826His(p.R826H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32800239:32800239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754182982
CDS Mutation	c.1846G>A
AA Mutation	p.Val616Met(p.V616M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32798602:32798602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372550911
CDS Mutation	c.1633C>T
AA Mutation	p.Arg545Cys(p.R545C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32799285:32799285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716G>C
AA Mutation	p.Arg572Ser(p.R572S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32780363:32780363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770859652
CDS Mutation	c.40G>A
AA Mutation	p.Ala14Thr(p.A14T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32781361:32781361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151T>A
AA Mutation	p.Ser51Thr(p.S51T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32784816:32784816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263C>T
AA Mutation	p.Pro88Leu(p.P88L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32799296:32799296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757889243
CDS Mutation	c.1727G>A
AA Mutation	p.Arg576Gln(p.R576Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32787333:32787333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536G>T
AA Mutation	p.Gly179Val(p.G179V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32801301:32801301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749860839
CDS Mutation	c.2020G>A
AA Mutation	p.Glu674Lys(p.E674K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32800870:32800870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761787019
CDS Mutation	c.1941C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32787337:32787337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32787358:32787358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.561C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32800274:32800274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17123657
CDS Mutation	c.1881C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32784787:32784787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32793571:32793571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32806241:32806241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531545763
CDS Mutation	c.2334G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32784772:32784772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32806268:32806268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369258965
CDS Mutation	c.2361A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32801396:32801396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759599570
CDS Mutation	c.2115C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328111
Start	32796845:32796845(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1359delG
AA Mutation	p.Leu454SerfsTer136(p.L454Sfs*136)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328111
Start	32787354:32787354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.561delC
AA Mutation	p.Tyr188ThrfsTer4(p.Y188Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000328111
Start	32795420:32795420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376213530
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Ter(p.R380*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000328111
Start	32786505:32786505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Ter(p.R104*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DNMT3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32801301:32801301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749860839
CDS Mutation	c.2020G>A
AA Mutation	p.Glu674Lys(p.E674K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32800227:32800227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762537914
CDS Mutation	c.1834G>A
AA Mutation	p.Ala612Thr(p.A612T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32802448:32802448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2209G>A
AA Mutation	p.Gly737Ser(p.G737S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32795658:32795658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>A
AA Mutation	p.Ala421Thr(p.A421T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32780420:32780420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773918660
CDS Mutation	c.97G>A
AA Mutation	p.Asp33Asn(p.D33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32791683:32791683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896G>A
AA Mutation	p.Arg299Gln(p.R299Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328111
Start	32787255:32787255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147421711
CDS Mutation	c.458C>T
AA Mutation	p.Ser153Leu(p.S153L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32801396:32801396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759599570
CDS Mutation	c.2115C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32806241:32806241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531545763
CDS Mutation	c.2334G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328111
Start	32796839:32796839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000328111
Start	32791682:32791682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Ter(p.R299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000328111
Start	32784860:32784860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript