Colon Cancer: Gene >> VRK3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316763
Start	49988374:49988374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215G>T
AA Mutation	p.Gln405His(p.Q405H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316763
Start	49979138:49979138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Cys(p.R461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316763
Start	49989762:49989762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61745859
CDS Mutation	c.973G>T
AA Mutation	p.Ala325Ser(p.A325S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316763
Start	49989763:49989763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972G>T
AA Mutation	p.Leu324Phe(p.L324F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316763
Start	49979181:49979181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745340857
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000316763
Start	50007626:50007626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779890225
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Ter(p.R164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VRK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316763
Start	49988430:49988430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159T>C
AA Mutation	p.Phe387Leu(p.F387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript