Colon Cancer: Gene >> VPS33A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267199
Start	122242421:122242421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057A>G
AA Mutation	p.Asn353Asp(p.N353D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267199
Start	122266336:122266336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267199
Start	122263659:122263659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767876880
CDS Mutation	c.209G>A
AA Mutation	p.Arg70His(p.R70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267199
Start	122232817:122232817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1592C>T
AA Mutation	p.Thr531Ile(p.T531I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267199
Start	122238719:122238719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780391563
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267199
Start	122250989:122250989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370198408
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267199
Start	122261276:122261276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267199
Start	122266388:122266388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776504041
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267199
Start	122249914:122249914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267199
Start	122239929:122239929(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1113delT
AA Mutation	p.Phe371LeufsTer4(p.F371Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267199
Start	122235850:122235850(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1376delG
AA Mutation	p.Gly459AlafsTer86(p.G459Afs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267199
Start	122263681:122263681(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.187delA
AA Mutation	p.Met63CysfsTer14(p.M63Cfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267199
Start	122232382:122232382(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1655delG
AA Mutation	p.Gly552AlafsTer2(p.G552Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267199
Start	122263622:122263622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs756221452
CDS Mutation	c.246delT
AA Mutation	p.Phe82LeufsTer6(p.F82Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267199
Start	122235849:122235850(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1376dupG
AA Mutation	p.Arg460GlnfsTer17(p.R460Qfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000267199
Start	122232969:122232969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1441-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> VPS33A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267199
Start	122238646:122238646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774697260
CDS Mutation	c.1243G>A
AA Mutation	p.Val415Met(p.V415M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267199
Start	122238620:122238620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269A>C
AA Mutation	p.Lys423Asn(p.K423N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript