Colon Cancer: Gene >> PRPF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150334994:150334994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788G>A
AA Mutation	p.Arg263His(p.R263H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150344171:150344171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436C>A
AA Mutation	p.Ser479Tyr(p.S479Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150346044:150346044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667A>C
AA Mutation	p.Lys556Thr(p.K556T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150346430:150346430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782T>G
AA Mutation	p.Phe594Leu(p.F594L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150344233:150344233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1498G>A
AA Mutation	p.Val500Ile(p.V500I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150335233:150335233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Trp(p.R343W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150343425:150343425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399G>T
AA Mutation	p.Gly467Cys(p.G467C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150335153:150335153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375374507
CDS Mutation	c.947C>T
AA Mutation	p.Ser316Phe(p.S316F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324862
Start	150335134:150335134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.933delT
AA Mutation	p.Phe311LeufsTer69(p.F311Lfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000324862
Start	150346022:150346022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Ter(p.R549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000324862
Start	150328377:150328377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Ter(p.R112*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRPF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324862
Start	150325816:150325816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211G>A
AA Mutation	p.Glu71Lys(p.E71K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript