Colon Cancer: Gene >> ZNF763

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11978733:11978733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772129280
CDS Mutation	c.809C>A
AA Mutation	p.Ser270Tyr(p.S270Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11979087:11979087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376889281
CDS Mutation	c.1163C>T
AA Mutation	p.Ala388Val(p.A388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11977112:11977112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>C
AA Mutation	p.Arg26Ser(p.R26S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11978348:11978348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424A>C
AA Mutation	p.Lys142Gln(p.K142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11978835:11978835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758599967
CDS Mutation	c.911G>T
AA Mutation	p.Arg304Ile(p.R304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000358987
Start	11978150:11978150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>T
AA Mutation	p.Glu76Ter(p.E76*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358987
Start	11979016:11979017(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1098dupA
AA Mutation	p.Pro367ThrfsTer3(p.P367Tfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358987
Start	11978805:11978806(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.883dupT
AA Mutation	p.Trp295LeufsTer9(p.W295Lfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000358987
Start	11977432:11977432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF763

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11978385:11978385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461G>T
AA Mutation	p.Arg154Ile(p.R154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358987
Start	11978691:11978691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767A>G
AA Mutation	p.Tyr256Cys(p.Y256C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript