Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDON

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126015439:126015439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571859031
CDS Mutation	c.1000G>A
AA Mutation	p.Asp334Asn(p.D334N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125978365:125978365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3295G>A
AA Mutation	p.Ala1099Thr(p.A1099T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126005946:126005946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143213791
CDS Mutation	c.1664C>T
AA Mutation	p.Pro555Leu(p.P555L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125994348:125994348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2586T>G
AA Mutation	p.Phe862Leu(p.F862L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392693
Start	126019763:126019763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352C>A
AA Mutation	p.Leu118Ile(p.L118I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125961831:125961831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3524G>A
AA Mutation	p.Ser1175Asn(p.S1175N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126017243:126017243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773A>G
AA Mutation	p.Asp258Gly(p.D258G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126005767:126005767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1843T>A
AA Mutation	p.Tyr615Asn(p.Y615N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125961766:125961766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3589G>A
AA Mutation	p.Val1197Ile(p.V1197I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126021404:126021404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193G>A
AA Mutation	p.Gly65Arg(p.G65R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126018373:126018373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597T>G
AA Mutation	p.His199Gln(p.H199Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125981119:125981119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3206T>G
AA Mutation	p.Leu1069Arg(p.L1069R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125961865:125961865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757589429
CDS Mutation	c.3490G>A
AA Mutation	p.Ala1164Thr(p.A1164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125997225:125997225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2344G>A
AA Mutation	p.Val782Ile(p.V782I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126005829:126005829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781486713
CDS Mutation	c.1781A>G
AA Mutation	p.Tyr594Cys(p.Y594C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126019639:126019639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476A>G
AA Mutation	p.Lys159Arg(p.K159R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125961901:125961901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3454C>T
AA Mutation	p.Leu1152Phe(p.L1152F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125961795:125961795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771268293
CDS Mutation	c.3560G>A
AA Mutation	p.Arg1187His(p.R1187H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125978325:125978325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3335G>A
AA Mutation	p.Arg1112Gln(p.R1112Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126015270:126015270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169A>G
AA Mutation	p.His390Arg(p.H390R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125994999:125994999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141611214
CDS Mutation	c.2416C>T
AA Mutation	p.Arg806Trp(p.R806W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126005881:126005881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145492265
CDS Mutation	c.1729C>T
AA Mutation	p.Pro577Ser(p.P577S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126021365:126021365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232C>A
AA Mutation	p.His78Asn(p.H78N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126006051:126006051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559T>C
AA Mutation	p.Phe520Ser(p.F520S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	125981225:125981225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199957528
CDS Mutation	c.3100G>A
AA Mutation	p.Gly1034Arg(p.G1034R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	125983945:125983945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771769883
CDS Mutation	c.2922C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126018349:126018349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126023422:126023422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126001747:126001747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2130A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126001807:126001807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535317968
CDS Mutation	c.2070C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	125981181:125981181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126021330:126021330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126005927:126005927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1683T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	125997277:125997277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2292C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	125961812:125961812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3543A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	125983963:125983963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760389665
CDS Mutation	c.2904C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392693
Start	125994309:125994309(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2625delT
AA Mutation	p.Ser875ArgfsTer8(p.S875Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392693
Start	126010453:126010460(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1433_1440delCCCAAGCT
AA Mutation	p.Ser478TrpfsTer25(p.S478Wfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392693
Start	126005853:126005853(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1757delC
AA Mutation	p.Pro586HisfsTer28(p.P586Hfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392693
Start	126017269:126017270(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.746_747insACACACTCCAAGGTTACAG
AA Mutation	p.Ala250HisfsTer35(p.A250Hfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000392693
Start	126018329:126018329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763917724
CDS Mutation	c.640+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CDON

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126018343:126018343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>T
AA Mutation	p.Lys209Asn(p.K209N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126019658:126019658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Cys(p.R153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392693
Start	126005781:126005781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1829C>T
AA Mutation	p.Ala610Val(p.A610V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	125994342:125994342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2592C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392693
Start	126021264:126021264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000392693
Start	126004034:126004034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752726620
CDS Mutation	c.1894C>T
AA Mutation	p.Arg632Ter(p.R632*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript