Colon Cancer: Gene >> WWOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78424979:78424979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715C>A
AA Mutation	p.Leu239Ile(p.L239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78432720:78432720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024T>C
AA Mutation	p.Phe342Leu(p.F342L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78432712:78432712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016C>G
AA Mutation	p.Thr339Arg(p.T339R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	79211747:79211747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200815431
CDS Mutation	c.1196C>T
AA Mutation	p.Ala399Val(p.A399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78424895:78424895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370737224
CDS Mutation	c.631G>A
AA Mutation	p.Ala211Thr(p.A211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78425009:78425009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749277249
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Cys(p.R249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78424881:78424881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617T>C
AA Mutation	p.Val206Ala(p.V206A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78164270:78164270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497C>T
AA Mutation	p.Ser166Leu(p.S166L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78386915:78386915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572A>C
AA Mutation	p.Gln191Pro(p.Q191P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78164188:78164188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764089824
CDS Mutation	c.415G>A
AA Mutation	p.Glu139Lys(p.E139K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78164273:78164273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377356629
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000566780
Start	78109782:78109782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771850922
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000566780
Start	78386907:78386907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000566780
Start	78424978:78424978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000566780
Start	78432503:78432503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62034095
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000566780
Start	78386922:78386922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554077107
CDS Mutation	c.579T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000566780
Start	78432623:78432623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000566780
Start	78432515:78432515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.822delA
AA Mutation	p.Lys274AsnfsTer53(p.K274Nfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000566780
Start	78164284:78164284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751181600
CDS Mutation	c.511G>T
AA Mutation	p.Glu171Ter(p.E171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000566780
Start	78108475:78108475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587777248
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Ter(p.R54*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000566780
Start	78115011:78115012(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.266_267insCATTTAT
AA Mutation	p.Arg89SerfsTer10(p.R89Sfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WWOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78432624:78432624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>G
AA Mutation	p.Arg310Gly(p.R310G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78432510:78432510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814T>G
AA Mutation	p.Leu272Val(p.L272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000566780
Start	78115119:78115119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374A>G
AA Mutation	p.Lys125Arg(p.K125R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript