Colon Cancer: Gene >> WWC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168455506:168455506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2809C>A
AA Mutation	p.Gln937Lys(p.Q937K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168292264:168292264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112C>T
AA Mutation	p.Arg38Trp(p.R38W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168460728:168460728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781412597
CDS Mutation	c.2902G>A
AA Mutation	p.Val968Ile(p.V968I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168385351:168385351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370G>T
AA Mutation	p.Ala124Ser(p.A124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168441736:168441736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201924297
CDS Mutation	c.2335C>T
AA Mutation	p.Arg779Cys(p.R779C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168428042:168428042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770194537
CDS Mutation	c.1820C>T
AA Mutation	p.Thr607Met(p.T607M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168454057:168454057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2615C>T
AA Mutation	p.Thr872Ile(p.T872I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168460726:168460726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2900G>A
AA Mutation	p.Ser967Asn(p.S967N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168424011:168424011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760218601
CDS Mutation	c.1753G>A
AA Mutation	p.Ala585Thr(p.A585T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168455419:168455419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549137219
CDS Mutation	c.2722C>T
AA Mutation	p.Arg908Trp(p.R908W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168441716:168441716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749653075
CDS Mutation	c.2315G>A
AA Mutation	p.Arg772Gln(p.R772Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168464934:168464934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145892564
CDS Mutation	c.3122G>A
AA Mutation	p.Arg1041His(p.R1041H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168464956:168464956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168385317:168385317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168464842:168464842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374783660
CDS Mutation	c.3030G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265293
Start	168408544:168408544(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.762delG
AA Mutation	p.Ser255LeufsTer26(p.S255Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WWC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168431403:168431403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2239G>A
AA Mutation	p.Asp747Asn(p.D747N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265293
Start	168460741:168460741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771485054
CDS Mutation	c.2915G>A
AA Mutation	p.Arg972Gln(p.R972Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168414587:168414587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181A>T
AA Mutation	p.Glu394Val(p.E394V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168428769:168428769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1982G>T
AA Mutation	p.Arg661Leu(p.R661L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168423665:168423665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1407C>A
Mutation Classification	Silent
Feature Type	Transcript