Colon Cancer: Gene >> PCGF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611883
Start	38739106:38739106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278G>A
AA Mutation	p.Arg93Gln(p.R93Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611883
Start	38735468:38735468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790C>T
AA Mutation	p.Pro264Ser(p.P264S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000611883
Start	38736149:38736149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747215640
CDS Mutation	c.598G>A
AA Mutation	p.Glu200Lys(p.E200K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000611883
Start	38738832:38738832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779878626
CDS Mutation	c.346G>A
AA Mutation	p.Glu116Lys(p.E116K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000611883
Start	38740321:38740321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611883
Start	38735505:38735505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000611883
Start	38740334:38740334(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.69delG
AA Mutation	p.Tyr24ThrfsTer44(p.Y24Tfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000611883
Start	38736098:38736099(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.648_649insA
AA Mutation	p.Trp217MetfsTer41(p.W217Mfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000611883
Start	38739585:38739585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000611883
Start	38735475:38735477(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.781_783delGAC
AA Mutation	p.Asp261del(p.D261del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PCGF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611883
Start	38739604:38739604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191G>A
AA Mutation	p.Arg64Gln(p.R64Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript