Colon Cancer: Gene >> WIPF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174567145:174567145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761503886
CDS Mutation	c.1381G>A
AA Mutation	p.Asp461Asn(p.D461N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174572392:174572392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413C>T
AA Mutation	p.Ala138Val(p.A138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174572128:174572128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770503150
CDS Mutation	c.677G>A
AA Mutation	p.Arg226His(p.R226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174571912:174571912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575913592
CDS Mutation	c.893C>T
AA Mutation	p.Pro298Leu(p.P298L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174567154:174567154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372C>G
AA Mutation	p.Pro458Ala(p.P458A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174575318:174575318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770105478
CDS Mutation	c.244G>A
AA Mutation	p.Gly82Arg(p.G82R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174571777:174571777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1028C>T
AA Mutation	p.Ser343Leu(p.S343L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174575327:174575327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531744802
CDS Mutation	c.235G>A
AA Mutation	p.Gly79Arg(p.G79R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174567152:174567152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757711719
CDS Mutation	c.1374G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174585544:174585544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745425874
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174571764:174571764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174572388:174572388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174575331:174575331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772302114
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359761
Start	174572143:174572143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.662delC
AA Mutation	p.Pro221LeufsTer20(p.P221Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359761
Start	174562603:174562603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000359761
Start	174567155:174567156(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1370_1371insAATACTCAC
AA Mutation	p.His457delinsGlnIleLeuThr(p.H457delinsQILT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WIPF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174567168:174567168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358G>T
AA Mutation	p.Arg453Ile(p.R453I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174571796:174571796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Trp(p.R337W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174571732:174571732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1073C>A
AA Mutation	p.Pro358His(p.P358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174572098:174572098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.707G>A
AA Mutation	p.Arg236His(p.R236H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174567876:174567876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1327G>A
AA Mutation	p.Asp443Asn(p.D443N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359761
Start	174567079:174567079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447G>A
AA Mutation	p.Glu483Lys(p.E483K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174575328:174575328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771529566
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174572187:174572187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762372137
CDS Mutation	c.618G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359761
Start	174585541:174585541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775206272
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript