Colon Cancer: Gene >> KIF3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132702133:132702133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757G>A
AA Mutation	p.Arg586Gln(p.R586Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132702208:132702208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1682C>G
AA Mutation	p.Ala561Gly(p.A561G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132726375:132726375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132703577:132703577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1271C>T
AA Mutation	p.Ala424Val(p.A424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132715877:132715877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771666064
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Trp(p.R337W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132702098:132702098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768023298
CDS Mutation	c.1792C>T
AA Mutation	p.Arg598Trp(p.R598W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132702185:132702185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1705A>G
AA Mutation	p.Arg569Gly(p.R569G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132734308:132734308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177G>T
AA Mutation	p.Lys59Asn(p.K59N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132734437:132734437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48G>T
AA Mutation	p.Lys16Asn(p.K16N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132716946:132716946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Cys(p.R219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132710978:132710978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209G>T
AA Mutation	p.Glu403Asp(p.E403D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000378746
Start	132726202:132726202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Ter(p.R146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000378746
Start	132734319:132734319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>T
AA Mutation	p.Glu56Ter(p.E56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KIF3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132702154:132702154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736G>A
AA Mutation	p.Arg579Gln(p.R579Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378746
Start	132702969:132702969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482G>T
AA Mutation	p.Glu494Asp(p.E494D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000378746
Start	132702902:132702902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549G>T
AA Mutation	p.Glu517Ter(p.E517*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript