Colon Cancer: Gene >> PHF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28910291:28910291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765Gln(p.R765Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28924058:28924058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566A>G
AA Mutation	p.Asp189Gly(p.D189G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28911216:28911216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139914566
CDS Mutation	c.2111C>T
AA Mutation	p.Thr704Met(p.T704M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28910238:28910238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2347C>T
AA Mutation	p.His783Tyr(p.H783Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28919181:28919181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931G>T
AA Mutation	p.Gly311Cys(p.G311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28906436:28906436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147060998
CDS Mutation	c.2762G>A
AA Mutation	p.Arg921Gln(p.R921Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28913982:28913982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746254087
CDS Mutation	c.1190C>T
AA Mutation	p.Ala397Val(p.A397V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28950171:28950171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Trp(p.R48W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332830
Start	28923931:28923931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.693G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332830
Start	28908814:28908814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2427C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332830
Start	28912873:28912873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1698A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332830
Start	28921766:28921766(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.758delA
AA Mutation	p.Asn253MetfsTer9(p.N253Mfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332830
Start	28906891:28906891(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2645delC
AA Mutation	p.Pro882GlnfsTer30(p.P882Qfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332830
Start	28950219:28950220(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.93dupC
AA Mutation	p.Lys32GlnfsTer13(p.K32Qfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PHF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28913232:28913232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1339T>G
AA Mutation	p.Leu447Val(p.L447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332830
Start	28917382:28917382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>T
AA Mutation	p.Ser346Leu(p.S346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript