Colon Cancer: Gene >> PLP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103789345:103789345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709T>A
AA Mutation	p.Phe237Ile(p.F237I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103786619:103786619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346A>T
AA Mutation	p.Thr116Ser(p.T116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103786683:103786683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410G>A
AA Mutation	p.Arg137Gln(p.R137Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103786616:103786616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103786580:103786580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>A
AA Mutation	p.Asp103Asn(p.D103N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000612423
Start	103785734:103785734(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.161delA
AA Mutation	p.Asn54ThrfsTer11(p.N54Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103785730:103785730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>A
AA Mutation	p.Phe51Leu(p.F51L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612423
Start	103785714:103785714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137T>A
AA Mutation	p.Leu46Gln(p.L46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript