Colon Cancer: Gene >> ZNF133

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18316355:18316355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1504G>T
AA Mutation	p.Gly502Cys(p.G502C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18315303:18315303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18315998:18315998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759777950
CDS Mutation	c.1147G>A
AA Mutation	p.Ala383Thr(p.A383T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18316559:18316559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755489447
CDS Mutation	c.1708C>T
AA Mutation	p.Arg570Trp(p.R570W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18316689:18316689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1838G>T
AA Mutation	p.Arg613Leu(p.R613L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18316266:18316266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415G>A
AA Mutation	p.Gly472Asp(p.G472D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18315095:18315095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772813491
CDS Mutation	c.244G>A
AA Mutation	p.Asp82Asn(p.D82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316358
Start	18316523:18316523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672G>A
AA Mutation	p.Gly558Ser(p.G558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316358
Start	18316495:18316495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1644G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316358
Start	18316561:18316561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748544558
CDS Mutation	c.1710G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316358
Start	18316087:18316087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2424156
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316358
Start	18316396:18316396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761524657
CDS Mutation	c.1545G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316358
Start	18315161:18315161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.315delC
AA Mutation	p.Trp106GlyfsTer81(p.W106Gfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316358
Start	18306364:18306364(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766297694
CDS Mutation	c.195delA
AA Mutation	p.Lys65AsnfsTer122(p.K65Nfs*122)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316358
Start	18306363:18306364(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs753775995
CDS Mutation	c.195dupA
AA Mutation	p.Cys66MetfsTer37(p.C66Mfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF133

No Mutation Annotation!