Colon Cancer: Gene >> ALPI

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000295463
Start	232456582:232456582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187T>A
AA Mutation	p.Leu63Met(p.L63M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232458285:232458285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151137290
CDS Mutation	c.1060G>A
AA Mutation	p.Asp354Asn(p.D354N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232458940:232458940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758104990
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Cys(p.R461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232456634:232456634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239G>A
AA Mutation	p.Gly80Asp(p.G80D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232458884:232458884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1325C>T
AA Mutation	p.Ala442Val(p.A442V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232457641:232457641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725A>G
AA Mutation	p.Gln242Arg(p.Q242R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232458109:232458109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374647501
CDS Mutation	c.968G>A
AA Mutation	p.Arg323His(p.R323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295463
Start	232458054:232458054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913C>A
AA Mutation	p.Pro305Thr(p.P305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295463
Start	232458741:232458741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295463
Start	232457836:232457836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766051572
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295463
Start	232458666:232458666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295463
Start	232458888:232458888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ALPI

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295463
Start	232457202:232457202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780862777
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript