Colon Cancer: Gene >> ZNF382

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626277:36626277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142570474
CDS Mutation	c.380G>A
AA Mutation	p.Arg127His(p.R127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626844:36626844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747367431
CDS Mutation	c.947G>A
AA Mutation	p.Arg316Gln(p.R316Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626235:36626235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772538250
CDS Mutation	c.338G>A
AA Mutation	p.Arg113Lys(p.R113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626982:36626982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757614823
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362His(p.R362H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626235:36626235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>T
AA Mutation	p.Arg113Ile(p.R113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626272:36626272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375G>T
AA Mutation	p.Lys125Asn(p.K125N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36627279:36627279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1382A>G
AA Mutation	p.Glu461Gly(p.E461G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626963:36626963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766247460
CDS Mutation	c.1066G>A
AA Mutation	p.Asp356Asn(p.D356N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626910:36626910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Ala338Val(p.A338V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626610:36626610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713G>T
AA Mutation	p.Arg238Ile(p.R238I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36627264:36627264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367G>T
AA Mutation	p.Arg456Ile(p.R456I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626811:36626811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914T>C
AA Mutation	p.Phe305Ser(p.F305S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626566:36626566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669G>A
AA Mutation	p.Met223Ile(p.M223I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36627180:36627180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283G>T
AA Mutation	p.Arg428Ile(p.R428I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292928
Start	36627274:36627274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761091621
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292928
Start	36610693:36610693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292928
Start	36627118:36627118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780590866
CDS Mutation	c.1221G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292928
Start	36627279:36627279(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1386delA
AA Mutation	p.Lys462AsnfsTer83(p.K462Nfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292928
Start	36627274:36627274(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1381delG
AA Mutation	p.Glu461LysfsTer84(p.E461Kfs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF382

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626244:36626244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760253473
CDS Mutation	c.347T>C
AA Mutation	p.Ile116Thr(p.I116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36627096:36627096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4439880
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400Lys(p.R400K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36627264:36627264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367G>T
AA Mutation	p.Arg456Ile(p.R456I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626351:36626351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533817629
CDS Mutation	c.454A>G
AA Mutation	p.Arg152Gly(p.R152G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626165:36626165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268T>A
AA Mutation	p.Phe90Ile(p.F90I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292928
Start	36626760:36626760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863G>T
AA Mutation	p.Arg288Ile(p.R288I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292928
Start	36610004:36610004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763656165
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000292928
Start	36627362:36627362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465G>T
AA Mutation	p.Glu489Ter(p.E489*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292928
Start	36627273:36627274(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1381dupG
AA Mutation	p.Glu461GlyfsTer7(p.E461Gfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript