Colon Cancer: Gene >> NUP153

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17669296:17669296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011T>A
AA Mutation	p.Asn337Lys(p.N337K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17616572:17616572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200059221
CDS Mutation	c.4298C>T
AA Mutation	p.Ser1433Leu(p.S1433L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17629140:17629140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3059C>A
AA Mutation	p.Ala1020Glu(p.A1020E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17625814:17625814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3895T>G
AA Mutation	p.Ser1299Ala(p.S1299A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17674976:17674976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>A
AA Mutation	p.Pro261Thr(p.P261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17629093:17629093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374947018
CDS Mutation	c.3106G>A
AA Mutation	p.Ala1036Thr(p.A1036T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17637765:17637765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758438447
CDS Mutation	c.1852G>A
AA Mutation	p.Ala618Thr(p.A618T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17628907:17628907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3292T>C
AA Mutation	p.Phe1098Leu(p.F1098L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17675311:17675311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641G>A
AA Mutation	p.Arg214His(p.R214H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17665382:17665382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072G>C
AA Mutation	p.Asp358His(p.D358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17629022:17629022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3177A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17625974:17625974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3735A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17629514:17629514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749852957
CDS Mutation	c.2685G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17637373:17637373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763230597
CDS Mutation	c.2244G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17706283:17706283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17624697:17624697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4038T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262077
Start	17628983:17628983(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3216delA
AA Mutation	p.Glu1073LysfsTer44(p.E1073Kfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262077
Start	17662054:17662054(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1232delA
AA Mutation	p.Asn411IlefsTer2(p.N411Ifs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262077
Start	17649257:17649258(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1438_1439delAC
AA Mutation	p.Thr480GlnfsTer8(p.T480Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000262077
Start	17675315:17675315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>T
AA Mutation	p.Glu213Ter(p.E213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262077
Start	17665380:17665381(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1073_1074insCTTCTTATCTA
AA Mutation	p.Ser359PhefsTer14(p.S359Ffs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262077
Start	17675267:17675268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.684dupA
AA Mutation	p.Pro229ThrfsTer22(p.P229Tfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NUP153

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17637765:17637765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758438447
CDS Mutation	c.1852G>A
AA Mutation	p.Ala618Thr(p.A618T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17637402:17637402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2215G>A
AA Mutation	p.Ala739Thr(p.A739T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262077
Start	17675614:17675614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Phe(p.S164F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262077
Start	17637373:17637373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763230597
CDS Mutation	c.2244G>A
Mutation Classification	Silent
Feature Type	Transcript