Colon Cancer: Gene >> APOD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343267
Start	195571334:195571334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>C
AA Mutation	p.Glu93Gln(p.E93Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343267
Start	195569126:195569126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs5954
CDS Mutation	c.344C>T
AA Mutation	p.Ser115Leu(p.S115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343267
Start	195569100:195569100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201787147
CDS Mutation	c.370G>A
AA Mutation	p.Asp124Asn(p.D124N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343267
Start	195579409:195579409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53C>T
AA Mutation	p.Ala18Val(p.A18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343267
Start	195573942:195573942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153G>T
AA Mutation	p.Lys51Asn(p.K51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343267
Start	195568903:195568903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200510277
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343267
Start	195568976:195568976(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.494delA
AA Mutation	p.Asn165IlefsTer3(p.N165Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> APOD

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000343267
Start	195573852:195573852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243G>C
AA Mutation	p.Leu81Phe(p.L81F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343267
Start	195569102:195569102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368C>T
AA Mutation	p.Thr123Ile(p.T123I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript