Colon Cancer: Gene >> AP3B2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82677676:82677676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766260323
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458His(p.R458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82659703:82659703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3106G>T
AA Mutation	p.Gly1036Trp(p.G1036W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82659667:82659667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3142A>G
AA Mutation	p.Thr1048Ala(p.T1048A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82677752:82677752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297A>G
AA Mutation	p.Ile433Val(p.I433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82665554:82665554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1874G>A
AA Mutation	p.Gly625Asp(p.G625D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82662820:82662820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760395320
CDS Mutation	c.2650G>A
AA Mutation	p.Gly884Arg(p.G884R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82666861:82666861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750333792
CDS Mutation	c.1738C>T
AA Mutation	p.Arg580Cys(p.R580C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82677719:82677719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82677793:82677793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750705900
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419His(p.R419H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82666870:82666870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754527481
CDS Mutation	c.1729G>A
AA Mutation	p.Asp577Asn(p.D577N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82662203:82662203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2826C>A
AA Mutation	p.Phe942Leu(p.F942L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82681562:82681562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379C>T
AA Mutation	p.Arg127Cys(p.R127C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82662894:82662894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529642370
CDS Mutation	c.2576G>A
AA Mutation	p.Arg859Gln(p.R859Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82676499:82676499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1627A>G
AA Mutation	p.Asn543Asp(p.N543D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82664452:82664452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2119A>T
AA Mutation	p.Ser707Cys(p.S707C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261722
Start	82662827:82662827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2643T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261722
Start	82662176:82662176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2853C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261722
Start	82663888:82663888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143109436
CDS Mutation	c.2292C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261722
Start	82663199:82663199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2475A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AP3B2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82677746:82677746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303C>T
AA Mutation	p.Arg435Cys(p.R435C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261722
Start	82662700:82662700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750043916
CDS Mutation	c.2770G>A
AA Mutation	p.Glu924Lys(p.E924K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261722
Start	82659620:82659620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540715932
CDS Mutation	c.3189C>T
Mutation Classification	Silent
Feature Type	Transcript