Colon Cancer: Gene >> CTNNBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37732904:37732904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56G>A
AA Mutation	p.Arg19Gln(p.R19Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37737444:37737444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286A>C
AA Mutation	p.Asn96His(p.N96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37871975:37871975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654G>A
AA Mutation	p.Glu552Lys(p.E552K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37802928:37802928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764634448
CDS Mutation	c.1093G>A
AA Mutation	p.Glu365Lys(p.E365K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37732934:37732934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779142999
CDS Mutation	c.86G>A
AA Mutation	p.Arg29His(p.R29H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37779237:37779237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>T
AA Mutation	p.Glu311Asp(p.E311D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37779328:37779328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1024A>G
AA Mutation	p.Met342Val(p.M342V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361383
Start	37737401:37737401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361383
Start	37779303:37779303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373840043
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361383
Start	37733014:37733014(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs761516328
CDS Mutation	c.172delA
AA Mutation	p.Arg58GlyfsTer25(p.R58Gfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTNNBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37746598:37746598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774420988
CDS Mutation	c.457G>A
AA Mutation	p.Asp153Asn(p.D153N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361383
Start	37732897:37732897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762613570
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript