Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF354C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079858:179079858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426G>T
AA Mutation	p.Ala476Ser(p.A476S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179078772:179078772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340T>C
AA Mutation	p.Ser114Pro(p.S114P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179078971:179078971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539G>A
AA Mutation	p.Ser180Asn(p.S180N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079643:179079643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143036580
CDS Mutation	c.1211G>A
AA Mutation	p.Arg404Gln(p.R404Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179078726:179078726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>T
AA Mutation	p.Gln98His(p.Q98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079439:179079439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007C>T
AA Mutation	p.Ala336Val(p.A336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079711:179079711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1279T>C
AA Mutation	p.Phe427Leu(p.F427L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079399:179079399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967A>G
AA Mutation	p.Thr323Ala(p.T323A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079697:179079697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1265A>G
AA Mutation	p.Asn422Ser(p.N422S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079211:179079211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779T>C
AA Mutation	p.Leu260Pro(p.L260P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079391:179079391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761132435
CDS Mutation	c.959G>T
AA Mutation	p.Arg320Ile(p.R320I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079327:179079327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>T
AA Mutation	p.Pro299Ser(p.P299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079928:179079928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496T>C
AA Mutation	p.Met499Thr(p.M499T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315475
Start	179079422:179079422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373125160
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315475
Start	179079884:179079884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761541929
CDS Mutation	c.1452C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315475
Start	179078731:179078731(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.303delT
AA Mutation	p.Phe101LeufsTer2(p.F101Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000315475
Start	179078838:179078838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>T
AA Mutation	p.Glu136Ter(p.E136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000315475
Start	179079333:179079333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754826681
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Ter(p.R301*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000315475
Start	179079762:179079762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330G>T
AA Mutation	p.Glu444Ter(p.E444*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315475
Start	179078840:179078841(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.408_409insTTAAT
AA Mutation	p.Glu137LeufsTer12(p.E137Lfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF354C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179077124:179077124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208C>T
AA Mutation	p.Pro70Ser(p.P70S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079239:179079239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807G>T
AA Mutation	p.Glu269Asp(p.E269D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079724:179079724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545360275
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431Gln(p.R431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000315475
Start	179078685:179078685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253T>G
AA Mutation	p.Phe85Val(p.F85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315475
Start	179079659:179079659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1227A>C
AA Mutation	p.Gln409His(p.Q409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315475
Start	179080001:179080001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569C>A
Mutation Classification	Silent
Feature Type	Transcript