Colon Cancer: Gene >> AP4M1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359593
Start	100105477:100105477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867C>A
AA Mutation	p.Asp289Glu(p.D289E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359593
Start	100106477:100106477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139861201
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367Gln(p.R367Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359593
Start	100105488:100105488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757649099
CDS Mutation	c.878C>T
AA Mutation	p.Pro293Leu(p.P293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359593
Start	100106800:100106800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1280C>T
AA Mutation	p.Ala427Val(p.A427V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359593
Start	100102746:100102746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762876619
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359593
Start	100104933:100104933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140144409
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359593
Start	100103423:100103423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359593
Start	100105471:100105471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142325884
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359593
Start	100104107:100104108(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.566dupT
AA Mutation	p.Leu189PhefsTer14(p.L189Ffs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AP4M1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359593
Start	100104131:100104131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.583T>G
AA Mutation	p.Leu195Val(p.L195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript