Colon Cancer: Gene >> WWP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86438606:86438606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771G>T
AA Mutation	p.Asp591Tyr(p.D591Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86461227:86461227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2503G>A
AA Mutation	p.Val835Met(p.V835M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86381509:86381509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Val72Ile(p.V72I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86448419:86448419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2179G>C
AA Mutation	p.Asp727His(p.D727H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86398446:86398446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>C
AA Mutation	p.Glu147Gln(p.E147Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86374075:86374075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25G>C
AA Mutation	p.Asp9His(p.D9H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86427765:86427765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753733811
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427Gln(p.R427Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86452576:86452576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527247142
CDS Mutation	c.2291G>A
AA Mutation	p.Arg764His(p.R764H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86448482:86448482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2242G>A
AA Mutation	p.Val748Met(p.V748M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86381552:86381552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371650373
CDS Mutation	c.257G>A
AA Mutation	p.Arg86His(p.R86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86438670:86438670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749190769
CDS Mutation	c.1835C>T
AA Mutation	p.Ala612Val(p.A612V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86411831:86411831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779921371
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Trp(p.R340W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86411850:86411850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>T
AA Mutation	p.Ala346Val(p.A346V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86435483:86435483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1633C>T
AA Mutation	p.Arg545Cys(p.R545C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86381588:86381588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750571078
CDS Mutation	c.293C>T
AA Mutation	p.Thr98Met(p.T98M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86430721:86430721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357G>T
AA Mutation	p.Asp453Tyr(p.D453Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86381559:86381559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264A>T
AA Mutation	p.Leu88Phe(p.L88F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86374054:86374054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86381563:86381563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>A
AA Mutation	p.Ala90Thr(p.A90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86411643:86411643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>A
AA Mutation	p.Thr277Asn(p.T277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265428
Start	86438594:86438594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1759T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265428
Start	86425274:86425274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265428
Start	86381514:86381514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559093201
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000265428
Start	86431406:86431406(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1393delA
AA Mutation	p.Arg465GlufsTer11(p.R465Efs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000265428
Start	86398356:86398356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>T
AA Mutation	p.Glu117Ter(p.E117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000265428
Start	86381558:86381558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263T>A
AA Mutation	p.Leu88Ter(p.L88*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000265428
Start	86448389:86448389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2149G>T
AA Mutation	p.Glu717Ter(p.E717*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WWP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86431665:86431665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61761628
CDS Mutation	c.1523G>A
AA Mutation	p.Arg508His(p.R508H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86452621:86452621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336G>A
AA Mutation	p.Gly779Asp(p.G779D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86380827:86380827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172A>G
AA Mutation	p.Ser58Gly(p.S58G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86425279:86425279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373Gln(p.R373Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86438625:86438625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1790A>G
AA Mutation	p.Tyr597Cys(p.Y597C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86442716:86442716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1936G>A
AA Mutation	p.Ala646Thr(p.A646T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265428
Start	86452606:86452606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2321A>C
AA Mutation	p.Lys774Thr(p.K774T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265428
Start	86380784:86380784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265428
Start	86430706:86430706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342T>C
Mutation Classification	Silent
Feature Type	Transcript