Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CTNNAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108952227:108952227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749689146
CDS Mutation	c.1817C>T
AA Mutation	p.Ser606Phe(p.S606F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108999136:108999136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Ala88Thr(p.A88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108999174:108999174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224T>A
AA Mutation	p.Val75Asp(p.V75D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108983254:108983254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150483984
CDS Mutation	c.791G>A
AA Mutation	p.Arg264His(p.R264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325551
Start	108984389:108984389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325551
Start	108999143:108999143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325551
Start	108999248:108999248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368581163
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325551
Start	108979434:108979434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325551
Start	109013347:109013359(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.84_96delGGGACTGGAGATC
AA Mutation	p.Gly29LysfsTer39(p.G29Kfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325551
Start	108965456:108965456(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1513delT
AA Mutation	p.Cys505ValfsTer15(p.C505Vfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTNNAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108999153:108999153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245T>G
AA Mutation	p.Phe82Cys(p.F82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108942776:108942776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2198A>C
AA Mutation	p.Lys733Thr(p.K733T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108979463:108979463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200532159
CDS Mutation	c.919C>T
AA Mutation	p.Arg307Trp(p.R307W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108999232:108999232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166G>T
AA Mutation	p.Asp56Tyr(p.D56Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108952213:108952213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831A>G
AA Mutation	p.Thr611Ala(p.T611A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108952300:108952300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548650160
CDS Mutation	c.1744G>A
AA Mutation	p.Glu582Lys(p.E582K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325551
Start	108983167:108983167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878T>G
AA Mutation	p.Phe293Cys(p.F293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript