Colon Cancer: Gene >> PRPF31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54128076:54128076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949G>T
AA Mutation	p.Gly317Cys(p.G317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54124516:54124516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715A>C
AA Mutation	p.Thr239Pro(p.T239P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54128361:54128361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756479054
CDS Mutation	c.1130G>A
AA Mutation	p.Arg377His(p.R377H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54126561:54126561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762463081
CDS Mutation	c.889G>A
AA Mutation	p.Ala297Thr(p.A297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54129069:54129069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159G>A
AA Mutation	p.Ala387Thr(p.A387T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54128193:54128193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066G>A
AA Mutation	p.Gly356Ser(p.G356S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321030
Start	54123802:54123802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581C>T
AA Mutation	p.Ala194Val(p.A194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321030
Start	54123860:54123860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000321030
Start	54124545:54124547(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.747_749delCAT
AA Mutation	p.Ile249del(p.I249del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRPF31

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321030
Start	54121879:54121879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750573765
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321030
Start	54122527:54122528(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.353_354insT
AA Mutation	p.Ser119LeufsTer6(p.S119Lfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript