Colon Cancer: Gene >> RREB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7210871:7210871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7229006:7229006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907G>A
AA Mutation	p.Glu303Lys(p.E303K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7247047:7247047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4432G>A
AA Mutation	p.Glu1478Lys(p.E1478K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7231623:7231623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3524G>A
AA Mutation	p.Ser1175Asn(p.S1175N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7231683:7231683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745990582
CDS Mutation	c.3584C>T
AA Mutation	p.Pro1195Leu(p.P1195L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7230982:7230982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883G>T
AA Mutation	p.Glu961Asp(p.E961D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7187518:7187518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256C>T
AA Mutation	p.Arg86Cys(p.R86C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7229024:7229024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925T>C
AA Mutation	p.Cys309Arg(p.C309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7229646:7229646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751013989
CDS Mutation	c.1547G>A
AA Mutation	p.Arg516Gln(p.R516Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7230152:7230152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2053G>A
AA Mutation	p.Ala685Thr(p.A685T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7230189:7230189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090G>A
AA Mutation	p.Arg697Gln(p.R697Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000349384
Start	7246423:7246423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3809-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RREB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7247168:7247168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4553A>G
AA Mutation	p.Asn1518Ser(p.N1518S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7231068:7231068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2969A>T
AA Mutation	p.Glu990Val(p.E990V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349384
Start	7231309:7231309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3210G>T
AA Mutation	p.Gln1070His(p.Q1070H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript