Colon Cancer: Gene >> NRBP1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000233557
Start	27441128:27441128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331T>C
AA Mutation	p.Val444Ala(p.V444A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27433362:27433362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89T>C
AA Mutation	p.Val30Ala(p.V30A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27436829:27436829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738G>T
AA Mutation	p.Glu246Asp(p.E246D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27433736:27433736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Val92Ile(p.V92I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27434547:27434547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512C>T
AA Mutation	p.Thr171Met(p.T171M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27435147:27435147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581G>A
AA Mutation	p.Cys194Tyr(p.C194Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27440879:27440879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268C>A
AA Mutation	p.Pro423His(p.P423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27439806:27439806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>A
AA Mutation	p.Arg315Lys(p.R315K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27441575:27441575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456A>C
AA Mutation	p.Ile486Leu(p.I486L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27440686:27440686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177T>G
AA Mutation	p.Phe393Val(p.F393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27440872:27440872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261A>G
AA Mutation	p.Thr421Ala(p.T421A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233557
Start	27440458:27440458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233557
Start	27437270:27437270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NRBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233557
Start	27441793:27441793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589C>T
AA Mutation	p.Ala530Val(p.A530V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233557
Start	27433279:27433279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749440672
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233557
Start	27441758:27441758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554C>T
Mutation Classification	Silent
Feature Type	Transcript