Colon Cancer: Gene >> CWC22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179973647:179973647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737G>A
AA Mutation	p.Arg246Gln(p.R246Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179964578:179964578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366C>T
AA Mutation	p.Arg456Cys(p.R456C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179945367:179945367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2489T>G
AA Mutation	p.Phe830Cys(p.F830C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179986780:179986780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375318426
CDS Mutation	c.121C>T
AA Mutation	p.Arg41Trp(p.R41W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179986722:179986722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761676860
CDS Mutation	c.179G>A
AA Mutation	p.Arg60His(p.R60H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179945638:179945638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218A>C
AA Mutation	p.Asn740His(p.N740H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179970805:179970805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992G>T
AA Mutation	p.Arg331Ile(p.R331I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179945370:179945370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2486C>A
AA Mutation	p.Ser829Tyr(p.S829Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179954340:179954340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554G>T
AA Mutation	p.Lys518Asn(p.K518N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179973753:179973753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631T>G
AA Mutation	p.Phe211Val(p.F211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179978278:179978278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493T>A
AA Mutation	p.Ser165Thr(p.S165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410053
Start	179945222:179945222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2634A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410053
Start	179950549:179950549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745417763
CDS Mutation	c.2103C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000410053
Start	179973693:179973693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>T
AA Mutation	p.Glu231Ter(p.E231*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000410053
Start	179945301:179945301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2555C>A
AA Mutation	p.Ser852Ter(p.S852*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CWC22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410053
Start	179973669:179973669(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	stop_gained
Transcription ID	ENST00000410053
Start	179945161:179945161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752315626
CDS Mutation	c.2695C>T
AA Mutation	p.Arg899Ter(p.R899*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000410053
Start	179945620:179945620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2236G>T
AA Mutation	p.Glu746Ter(p.E746*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000410053
Start	179986779:179986780(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.121dupC
AA Mutation	p.Arg41ProfsTer3(p.R41Pfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript