Colon Cancer: Gene >> KIF3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32311043:32311043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266G>T
AA Mutation	p.Glu422Asp(p.E422D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32309902:32309902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125C>T
AA Mutation	p.Ser42Phe(p.S42F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32310148:32310148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371A>G
AA Mutation	p.Asp124Gly(p.D124G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32330316:32330316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370914318
CDS Mutation	c.2144C>T
AA Mutation	p.Ala715Val(p.A715V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32310676:32310676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899T>C
AA Mutation	p.Leu300Pro(p.L300P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32310010:32310010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776291932
CDS Mutation	c.233G>A
AA Mutation	p.Arg78Gln(p.R78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375712
Start	32316547:32316547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375712
Start	32310302:32310302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375712
Start	32310545:32310545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200496440
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000375712
Start	32311023:32311023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246G>T
AA Mutation	p.Glu416Ter(p.E416*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KIF3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375712
Start	32310310:32310310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533A>G
AA Mutation	p.Asp178Gly(p.D178G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375712
Start	32309960:32309960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000375712
Start	32310567:32310567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790G>T
AA Mutation	p.Glu264Ter(p.E264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript