Colon Cancer: Gene >> DNMBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99955535:99955535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1939C>A
AA Mutation	p.Leu647Met(p.L647M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99884179:99884179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745738512
CDS Mutation	c.3829C>T
AA Mutation	p.Arg1277Trp(p.R1277W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99957154:99957154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320G>A
AA Mutation	p.Arg107Gln(p.R107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99886395:99886395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770587503
CDS Mutation	c.3523G>A
AA Mutation	p.Ala1175Thr(p.A1175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99886547:99886547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3371G>A
AA Mutation	p.Arg1124His(p.R1124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99956833:99956833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373777411
CDS Mutation	c.641C>T
AA Mutation	p.Ser214Phe(p.S214F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99900039:99900039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2582A>G
AA Mutation	p.Glu861Gly(p.E861G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99898097:99898097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755577741
CDS Mutation	c.2909G>A
AA Mutation	p.Arg970Gln(p.R970Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99955420:99955420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2054T>G
AA Mutation	p.Leu685Arg(p.L685R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99898139:99898139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752522080
CDS Mutation	c.2867C>T
AA Mutation	p.Ala956Val(p.A956V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99956140:99956140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1334A>G
AA Mutation	p.Asp445Gly(p.D445G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000324109
Start	99886301:99886301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770552124
CDS Mutation	c.3617C>T
AA Mutation	p.Ser1206Leu(p.S1206L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99956170:99956170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304G>T
AA Mutation	p.Gly435Val(p.G435V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99955606:99955606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1868C>A
AA Mutation	p.Pro623His(p.P623H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99955504:99955504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115222765
CDS Mutation	c.1970C>T
AA Mutation	p.Ala657Val(p.A657V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99956973:99956973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99956343:99956343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99956663:99956663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99956325:99956325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99879970:99879970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769113426
CDS Mutation	c.4389G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99956682:99956682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139271365
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324109
Start	99956892:99956892(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.582delT
AA Mutation	p.Pro195GlnfsTer5(p.P195Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324109
Start	99880168:99880168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4191delG
AA Mutation	p.Ser1398LeufsTer25(p.S1398Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324109
Start	99956066:99956066(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1408delA
AA Mutation	p.Thr470LeufsTer20(p.T470Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DNMBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99956662:99956662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812G>A
AA Mutation	p.Arg271Gln(p.R271Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99896308:99896308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3010G>T
AA Mutation	p.Val1004Phe(p.V1004F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99908036:99908036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2513C>T
AA Mutation	p.Ser838Leu(p.S838L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324109
Start	99955758:99955758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716A>C
AA Mutation	p.Lys572Asn(p.K572N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99880348:99880348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779422875
CDS Mutation	c.4011C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324109
Start	99969230:99969230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746639347
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript