Colon Cancer: Gene >> PRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70598652:70598652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757636984
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Trp(p.R357W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70598330:70598330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748060067
CDS Mutation	c.1391G>A
AA Mutation	p.Arg464Gln(p.R464Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70598417:70598417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28933376
CDS Mutation	c.1304C>T
AA Mutation	p.Thr435Met(p.T435M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70598391:70598391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330G>T
AA Mutation	p.Gly444Cys(p.G444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70598702:70598702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019A>G
AA Mutation	p.Asp340Gly(p.D340G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70599158:70599158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150156593
CDS Mutation	c.563C>T
AA Mutation	p.Pro188Leu(p.P188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70600820:70600820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83G>A
AA Mutation	p.Arg28His(p.R28H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70600557:70600557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>T
AA Mutation	p.Ala116Ser(p.A116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373209
Start	70600540:70600540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146358730
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373209
Start	70599106:70599106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141130900
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373209
Start	70600825:70600825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373209
Start	70600792:70600792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547321451
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373209
Start	70598854:70598854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373209
Start	70598293:70598293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs748926167
CDS Mutation	c.1428delG
AA Mutation	p.Leu478Ter(p.L478*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373209
Start	70598433:70598433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1288delG
AA Mutation	p.Asp430ThrfsTer10(p.D430Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000373209
Start	70598305:70598310(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1411_1416delCTCCTG
AA Mutation	p.Leu471_Leu472del(p.L471_L472del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373209
Start	70600769:70600769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>T
AA Mutation	p.Gly45Val(p.G45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript