Colon Cancer: Gene >> POF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85306202:85306202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296G>T
AA Mutation	p.Glu432Asp(p.E432D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85345974:85345974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>A
AA Mutation	p.His203Gln(p.H203Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85308159:85308159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200939713
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Trp(p.R339W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85307273:85307273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054C>G
AA Mutation	p.Leu352Val(p.L352V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85359594:85359594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394C>T
AA Mutation	p.Pro132Ser(p.P132S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85306218:85306218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200080276
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427His(p.R427H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262753
Start	85306304:85306304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262753
Start	85379318:85379318(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.137delA
AA Mutation	p.Asn46MetfsTer2(p.N46Mfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000262753
Start	85303467:85303467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588G>T
AA Mutation	p.Glu530Ter(p.E530*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262753
Start	85359600:85359601(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.386_387dupCT
AA Mutation	p.Thr130LeufsTer12(p.T130Lfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> POF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262753
Start	85307257:85307257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070T>G
AA Mutation	p.Met357Arg(p.M357R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript