Colon Cancer: Gene >> ZC3H12A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483475:37483475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1664G>T
AA Mutation	p.Ser555Ile(p.S555I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483573:37483573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193053985
CDS Mutation	c.1762G>A
AA Mutation	p.Glu588Lys(p.E588K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37481754:37481754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.737A>G
AA Mutation	p.Tyr246Cys(p.Y246C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37475711:37475711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215T>G
AA Mutation	p.Leu72Arg(p.L72R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483048:37483048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237A>G
AA Mutation	p.Ser413Gly(p.S413G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37480347:37480347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501T>G
AA Mutation	p.Phe167Leu(p.F167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37475723:37475723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Ala76Val(p.A76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37482536:37482536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186794112
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37481824:37481824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745695390
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37483402:37483402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1595delC
AA Mutation	p.Pro532GlnfsTer41(p.P532Qfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37480355:37480355(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.512delG
AA Mutation	p.Gly171AlafsTer60(p.G171Afs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373087
Start	37475799:37475799(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.306delC
AA Mutation	p.Cys103AlafsTer6(p.C103Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000373087
Start	37481625:37481627(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746760598
CDS Mutation	c.617_619delAGA
AA Mutation	p.Lys206del(p.K206del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZC3H12A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37481804:37481804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Trp(p.R263W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373087
Start	37483159:37483159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>T
AA Mutation	p.Leu450Phe(p.L450F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373087
Start	37481740:37481740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000373087
Start	37475845:37475845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349A>T
AA Mutation	p.Lys117Ter(p.K117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript