Colon Cancer: Gene >> ZNF217

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53571800:53571800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3091A>C
AA Mutation	p.Asn1031His(p.N1031H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53575816:53575816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2948T>C
AA Mutation	p.Val983Ala(p.V983A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53582234:53582234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593C>A
AA Mutation	p.Thr198Lys(p.T198K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53582409:53582409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766424905
CDS Mutation	c.418G>A
AA Mutation	p.Ala140Thr(p.A140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576152:53576152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2612C>A
AA Mutation	p.Pro871His(p.P871H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53582408:53582408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>A
AA Mutation	p.Ala140Asp(p.A140D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576108:53576108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112155907
CDS Mutation	c.2656G>A
AA Mutation	p.Ala886Thr(p.A886T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53575994:53575994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376210645
CDS Mutation	c.2770G>A
AA Mutation	p.Val924Met(p.V924M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576753:53576753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758311512
CDS Mutation	c.2011G>A
AA Mutation	p.Ala671Thr(p.A671T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53575795:53575795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371730112
CDS Mutation	c.2969A>G
AA Mutation	p.Tyr990Cys(p.Y990C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53578371:53578371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53571810:53571810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3081A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53582344:53582344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53581540:53581540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53582116:53582116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53581840:53581840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53582083:53582083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53575785:53575785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535784886
CDS Mutation	c.2979C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53576502:53576502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141041836
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53581570:53581570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766744159
CDS Mutation	c.1257G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53575896:53575896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756274423
CDS Mutation	c.2868G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53576268:53576268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540656868
CDS Mutation	c.2496C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302342
Start	53578378:53578378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1439delT
AA Mutation	p.Phe480SerfsTer35(p.F480Sfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302342
Start	53576687:53576687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2077delG
AA Mutation	p.Ala693LeufsTer10(p.A693Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302342
Start	53571748:53571749(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs757730974
CDS Mutation	c.3142dupA
AA Mutation	p.Thr1048AsnfsTer5(p.T1048Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF217

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53575980:53575980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2784C>G
AA Mutation	p.Asp928Glu(p.D928E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576168:53576168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2596G>A
AA Mutation	p.Val866Ile(p.V866I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576474:53576474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2290G>T
AA Mutation	p.Asp764Tyr(p.D764Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53581476:53581476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200131894
CDS Mutation	c.1351G>A
AA Mutation	p.Glu451Lys(p.E451K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576885:53576885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879A>C
AA Mutation	p.Lys627Gln(p.K627Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302342
Start	53571749:53571749(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3142delA
AA Mutation	p.Thr1048LeufsTer59(p.T1048Lfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript