Colon Cancer: Gene >> NWD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37443460:37443460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1472A>C
AA Mutation	p.Asp491Ala(p.D491A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37444386:37444386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398T>G
AA Mutation	p.Phe800Val(p.F800V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446177:37446177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4189G>A
AA Mutation	p.Gly1397Arg(p.G1397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37445730:37445730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3742G>A
AA Mutation	p.Ala1248Thr(p.A1248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37443859:37443859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1871G>A
AA Mutation	p.Arg624Lys(p.R624K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37430693:37430693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479G>T
AA Mutation	p.Trp160Leu(p.W160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446705:37446705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4717T>A
AA Mutation	p.Ser1573Thr(p.S1573T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000309447
Start	37356480:37356480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>C
AA Mutation	p.Val119Leu(p.V119L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37445341:37445341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3353A>G
AA Mutation	p.Tyr1118Cys(p.Y1118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37444666:37444666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2678C>T
AA Mutation	p.Ala893Val(p.A893V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37444795:37444795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2807A>G
AA Mutation	p.Asp936Gly(p.D936G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37356430:37356430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Arg102His(p.R102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37444545:37444545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749599296
CDS Mutation	c.2557G>A
AA Mutation	p.Gly853Ser(p.G853S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37444082:37444082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094C>A
AA Mutation	p.Ser698Arg(p.S698R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37444886:37444886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2898T>G
AA Mutation	p.Ser966Arg(p.S966R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446508:37446508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4520G>T
AA Mutation	p.Ser1507Ile(p.S1507I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37439053:37439053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959C>T
AA Mutation	p.Ser320Phe(p.S320F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37445804:37445804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3816A>C
AA Mutation	p.Glu1272Asp(p.E1272D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446401:37446401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4413G>T
AA Mutation	p.Lys1471Asn(p.K1471N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37443766:37443766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1778C>T
AA Mutation	p.Thr593Ile(p.T593I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37445082:37445082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3094A>G
AA Mutation	p.Thr1032Ala(p.T1032A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309447
Start	37245118:37245118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309447
Start	37444031:37444031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2043A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309447
Start	37444466:37444466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2478C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309447
Start	37444124:37444124(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2137delG
AA Mutation	p.Glu713ArgfsTer7(p.E713Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309447
Start	37445936:37445936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3951delA
AA Mutation	p.Lys1317AsnfsTer43(p.K1317Nfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309447
Start	37445757:37445757(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3775delT
AA Mutation	p.Trp1259GlyfsTer22(p.W1259Gfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000309447
Start	37446168:37446168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4180C>T
AA Mutation	p.Arg1394Ter(p.R1394*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000309447
Start	37438812:37438812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718G>T
AA Mutation	p.Glu240Ter(p.E240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309447
Start	37445769:37445770(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3784dupG
AA Mutation	p.Asp1262GlyfsTer18(p.D1262Gfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NWD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446039:37446039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4051G>A
AA Mutation	p.Glu1351Lys(p.E1351K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446169:37446169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4181G>A
AA Mutation	p.Arg1394Gln(p.R1394Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446582:37446582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4594A>C
AA Mutation	p.Ile1532Leu(p.I1532L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309447
Start	37446742:37446742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4754G>A
AA Mutation	p.Arg1585Gln(p.R1585Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309447
Start	37444472:37444472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2484C>T
Mutation Classification	Silent
Feature Type	Transcript