Colon Cancer: Gene >> ACRBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6638964:6638964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779982883
CDS Mutation	c.1499G>A
AA Mutation	p.Arg500His(p.R500H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6644290:6644290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791A>G
AA Mutation	p.Asn264Ser(p.N264S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6644291:6644291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790A>T
AA Mutation	p.Asn264Tyr(p.N264Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6646848:6646848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208A>G
AA Mutation	p.Asn70Asp(p.N70D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6638338:6638338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756765669
CDS Mutation	c.1576G>A
AA Mutation	p.Val526Ile(p.V526I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6644249:6644249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832A>G
AA Mutation	p.Thr278Ala(p.T278A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6644188:6644188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893T>C
AA Mutation	p.Met298Thr(p.M298T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6646881:6646881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175A>G
AA Mutation	p.Thr59Ala(p.T59A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6640197:6640197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140185383
CDS Mutation	c.1288G>A
AA Mutation	p.Gly430Arg(p.G430R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6638328:6638328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763758076
CDS Mutation	c.1586G>A
AA Mutation	p.Arg529Gln(p.R529Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229243
Start	6640352:6640352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752805695
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229243
Start	6638288:6638288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149312090
CDS Mutation	c.1626C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229243
Start	6640198:6640198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143853195
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229243
Start	6640370:6640370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229243
Start	6644433:6644433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000229243
Start	6639038:6639038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACRBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6640480:6640480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369836113
CDS Mutation	c.1120C>T
AA Mutation	p.Leu374Phe(p.L374F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6644195:6644195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886G>T
AA Mutation	p.Asp296Tyr(p.D296Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229243
Start	6645276:6645276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>A
AA Mutation	p.Ala140Asp(p.A140D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229243
Start	6646495:6646495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000229243
Start	6639038:6639038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript