Colon Cancer: Gene >> AP2M1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184178921:184178921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777567779
CDS Mutation	c.139G>A
AA Mutation	p.Val47Ile(p.V47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184180969:184180969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550C>T
AA Mutation	p.Leu184Phe(p.L184F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184180184:184180184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356G>A
AA Mutation	p.Gly119Asp(p.G119D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000292807
Start	184181815:184181815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827G>A
AA Mutation	p.Arg276Lys(p.R276K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184181917:184181917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184181976:184181976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Cys(p.R298C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184181109:184181109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590C>T
AA Mutation	p.Ser197Leu(p.S197L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292807
Start	184182180:184182180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755854980
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292807
Start	184183490:184183490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202236381
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292807
Start	184182844:184182845(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1155dupC
AA Mutation	p.Ile386HisfsTer6(p.I386Hfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AP2M1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292807
Start	184180211:184180211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383C>T
AA Mutation	p.Ala128Val(p.A128V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript