Colon Cancer: Gene >> VRK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96855311:96855311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664G>A
AA Mutation	p.Asp222Asn(p.D222N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96853159:96853159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569C>A
AA Mutation	p.Pro190His(p.P190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96855278:96855278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631A>C
AA Mutation	p.Lys211Gln(p.K211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96855339:96855339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757917768
CDS Mutation	c.692A>G
AA Mutation	p.Asp231Gly(p.D231G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96833568:96833568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97G>A
AA Mutation	p.Ala33Thr(p.A33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216639
Start	96833570:96833570(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.104delA
AA Mutation	p.Lys35ArgfsTer5(p.K35Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000216639
Start	96846110:96846110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>T
AA Mutation	p.Gly78Ter(p.G78*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000216639
Start	96860736:96860736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> VRK1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216639
Start	96876120:96876120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149083861
CDS Mutation	c.1159C>T
AA Mutation	p.Arg387Cys(p.R387C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96856237:96856237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>T
AA Mutation	p.Asp273Tyr(p.D273Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216639
Start	96852935:96852935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479G>T
AA Mutation	p.Arg160Ile(p.R160I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript