Colon Cancer: Gene >> VPS9D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389386
Start	89709275:89709275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1549G>A
AA Mutation	p.Gly517Arg(p.G517R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389386
Start	89716484:89716484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409G>A
AA Mutation	p.Ala137Thr(p.A137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389386
Start	89712099:89712099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607C>T
AA Mutation	p.Leu203Phe(p.L203F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389386
Start	89712663:89712663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485C>T
AA Mutation	p.Ala162Val(p.A162V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389386
Start	89709289:89709289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769008409
CDS Mutation	c.1535C>T
AA Mutation	p.Ala512Val(p.A512V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389386
Start	89708498:89708498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775227112
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389386
Start	89709252:89709252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389386
Start	89710704:89710704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389386
Start	89710614:89710614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369064538
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389386
Start	89716800:89716800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.198delC
AA Mutation	p.Asp67ThrfsTer6(p.D67Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389386
Start	89710897:89710897(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.947delC
AA Mutation	p.Pro316ArgfsTer93(p.P316Rfs*93)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389386
Start	89709313:89709314(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1510dupG
AA Mutation	p.Ala504GlyfsTer67(p.A504Gfs*67)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389386
Start	89711366:89711367(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.793dupG
AA Mutation	p.Asp265GlyfsTer127(p.D265Gfs*127)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> VPS9D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389386
Start	89710811:89710811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Trp(p.R345W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389386
Start	89709369:89709369(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1455delC
AA Mutation	p.Thr486ProfsTer47(p.T486Pfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript