Colon Cancer: Gene >> AP4B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113895415:113895415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368828060
CDS Mutation	c.1870C>T
AA Mutation	p.Arg624Cys(p.R624C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113896371:113896371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397C>T
AA Mutation	p.Ser466Leu(p.S466L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113900071:113900071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947A>C
AA Mutation	p.Lys316Thr(p.K316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113895129:113895129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564093511
CDS Mutation	c.2156C>T
AA Mutation	p.Thr719Met(p.T719M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113904708:113904708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10C>A
AA Mutation	p.Leu4Ile(p.L4I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113895135:113895135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199879996
CDS Mutation	c.2150C>T
AA Mutation	p.Thr717Met(p.T717M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113900065:113900065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953T>G
AA Mutation	p.Phe318Cys(p.F318C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256658
Start	113895346:113895346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1939C>T
AA Mutation	p.Pro647Ser(p.P647S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256658
Start	113895278:113895278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146869083
CDS Mutation	c.2007C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256658
Start	113900060:113900060(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775095423
CDS Mutation	c.958delT
AA Mutation	p.Cys320AlafsTer21(p.C320Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AP4B1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256658
Start	113900151:113900151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript