Colon Cancer: Gene >> BNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83264304:83264304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947A>G
AA Mutation	p.Asp316Gly(p.D316G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83266952:83266952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Cys(p.R107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263056:83263056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195C>A
AA Mutation	p.Ala732Asp(p.A732D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263397:83263397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1854T>A
AA Mutation	p.Ser618Arg(p.S618R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83262988:83262988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2263T>A
AA Mutation	p.Cys755Ser(p.C755S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83257593:83257593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2834C>T
AA Mutation	p.Ala945Val(p.A945V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83258081:83258081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2346A>C
AA Mutation	p.Glu782Asp(p.E782D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83258088:83258088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2339G>A
AA Mutation	p.Ser780Asn(p.S780N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83264322:83264322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929C>G
AA Mutation	p.Ala310Gly(p.A310G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83257524:83257524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2903C>T
AA Mutation	p.Ser968Leu(p.S968L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83266931:83266931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Trp(p.R114W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83257919:83257919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2508A>C
AA Mutation	p.Gln836His(p.Q836H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83262987:83262987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2264G>A
AA Mutation	p.Cys755Tyr(p.C755Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263761:83263761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757220105
CDS Mutation	c.1490C>T
AA Mutation	p.Thr497Met(p.T497M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83257516:83257516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766072426
CDS Mutation	c.2911C>T
AA Mutation	p.Arg971Cys(p.R971C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83267050:83267050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>A
AA Mutation	p.Pro74His(p.P74H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263206:83263206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765009276
CDS Mutation	c.2045G>A
AA Mutation	p.Gly682Glu(p.G682E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83264137:83264137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114C>A
AA Mutation	p.Leu372Ile(p.L372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263173:83263173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146647716
CDS Mutation	c.2078C>T
AA Mutation	p.Ala693Val(p.A693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263774:83263774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759909793
CDS Mutation	c.1477C>T
AA Mutation	p.Arg493Cys(p.R493C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83264322:83264322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929C>T
AA Mutation	p.Ala310Val(p.A310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263594:83263594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657A>C
AA Mutation	p.Ile553Leu(p.I553L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83264185:83264185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Trp(p.R356W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83263202:83263202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2049C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83264627:83264627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759840313
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83266869:83266869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83263913:83263913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376158536
CDS Mutation	c.1338G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83263736:83263736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1515T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83267025:83267025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749950118
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000345382
Start	83257510:83257510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749980467
CDS Mutation	c.2917C>T
AA Mutation	p.Arg973Ter(p.R973*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000345382
Start	83263606:83263606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645G>T
AA Mutation	p.Glu549Ter(p.E549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000345382
Start	83268131:83268131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> BNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83266952:83266952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Cys(p.R107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83258052:83258052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2375G>A
AA Mutation	p.Arg792His(p.R792H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345382
Start	83263277:83263277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1974C>A
AA Mutation	p.Phe658Leu(p.F658L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345382
Start	83264084:83264084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760326173
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript