Colon Cancer: Gene >> APLP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263574
Start	130130090:130130090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1508A>C
AA Mutation	p.Asp503Ala(p.D503A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263574
Start	130141570:130141570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773309208
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Trp(p.R678W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263574
Start	130140414:130140414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890G>T
AA Mutation	p.Glu630Asp(p.E630D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263574
Start	130126807:130126807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Trp(p.R400W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263574
Start	130141541:130141541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756337038
CDS Mutation	c.2003C>T
AA Mutation	p.Ala668Val(p.A668V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263574
Start	130122401:130122401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263574
Start	130120753:130120753(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.455delT
AA Mutation	p.Phe152SerfsTer18(p.F152Sfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> APLP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263574
Start	130109585:130109585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>A
AA Mutation	p.Leu88Ile(p.L88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263574
Start	130123735:130123735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046A>C
AA Mutation	p.Asn349Thr(p.N349T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263574
Start	130140432:130140432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112573341
CDS Mutation	c.1908C>T
Mutation Classification	Silent
Feature Type	Transcript