Colon Cancer: Gene >> ALPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232379918:232379918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>G
AA Mutation	p.Ile213Met(p.I213M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232378845:232378845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>A
AA Mutation	p.Leu15Met(p.L15M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232379814:232379814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>A
AA Mutation	p.Ala179Thr(p.A179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232379908:232379908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750382140
CDS Mutation	c.629C>T
AA Mutation	p.Thr210Met(p.T210M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232380998:232380998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>A
AA Mutation	p.Gly387Arg(p.G387R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232379841:232379841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142656870
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Cys(p.R188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232379818:232379818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539G>A
AA Mutation	p.Gly180Asp(p.G180D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232380442:232380442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148586042
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392027
Start	232381669:232381669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392027
Start	232381303:232381303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752955692
CDS Mutation	c.1245C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000392027
Start	232379937:232379937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ALPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392027
Start	232380734:232380734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766110386
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript