Colon Cancer: Gene >> ZEB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31520770:31520770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1435C>A
AA Mutation	p.Leu479Ile(p.L479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521652:31521652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754135071
CDS Mutation	c.2317G>A
AA Mutation	p.Ala773Thr(p.A773T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521514:31521514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2179C>A
AA Mutation	p.Gln727Lys(p.Q727K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521855:31521855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2520G>T
AA Mutation	p.Gln840His(p.Q840H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31520328:31520328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.993G>T
AA Mutation	p.Lys331Asn(p.K331N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521878:31521878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759615272
CDS Mutation	c.2543C>T
AA Mutation	p.Thr848Met(p.T848M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521469:31521469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2134T>A
AA Mutation	p.Ser712Thr(p.S712T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521652:31521652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317G>T
AA Mutation	p.Ala773Ser(p.A773S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31526774:31526774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2885G>C
AA Mutation	p.Cys962Ser(p.C962S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31520350:31520350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015G>C
AA Mutation	p.Glu339Gln(p.E339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521326:31521326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141110915
CDS Mutation	c.1991C>A
AA Mutation	p.Ser664Tyr(p.S664Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31520320:31520320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754576407
CDS Mutation	c.985C>T
AA Mutation	p.Arg329Trp(p.R329W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31521818:31521818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2483C>T
AA Mutation	p.Ala828Val(p.A828V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320985
Start	31527096:31527096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765424726
CDS Mutation	c.3207G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320985
Start	31521636:31521636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2301C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320985
Start	31520533:31520533(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1199delG
AA Mutation	p.Gly400ValfsTer6(p.G400Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320985
Start	31527059:31527059(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3174delA
AA Mutation	p.Lys1058AsnfsTer20(p.K1058Nfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000320985
Start	31526743:31526743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2854C>T
AA Mutation	p.Arg952Ter(p.R952*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000320985
Start	31502509:31502509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481G>T
AA Mutation	p.Gly161Ter(p.G161*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320985
Start	31521630:31521631(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2295_2296insAGGTTTAGAG
AA Mutation	p.Glu766ArgfsTer57(p.E766Rfs*57)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZEB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31520830:31520830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139511659
CDS Mutation	c.1495G>A
AA Mutation	p.Ala499Thr(p.A499T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320985
Start	31524021:31524021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35653460
CDS Mutation	c.2690G>A
AA Mutation	p.Arg897Gln(p.R897Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320985
Start	31461152:31461152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760520181
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript