Colon Cancer: Gene >> VPS51

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279281
Start	65107634:65107634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279281
Start	65109794:65109794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1749G>T
AA Mutation	p.Gln583His(p.Q583H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279281
Start	65109918:65109918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780357113
CDS Mutation	c.1873G>A
AA Mutation	p.Val625Met(p.V625M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279281
Start	65108405:65108405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>T
AA Mutation	p.Val312Leu(p.V312L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000279281
Start	65111547:65111547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309T>C
AA Mutation	p.Met770Thr(p.M770T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279281
Start	65107912:65107912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279281
Start	65107684:65107684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765356754
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279281
Start	65109782:65109782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377010488
CDS Mutation	c.1737C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279281
Start	65109412:65109412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VPS51

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279281
Start	65111474:65111474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2236G>A
AA Mutation	p.Glu746Lys(p.E746K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript