Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNFX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49263445:49263445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2190T>G
AA Mutation	p.His730Gln(p.H730Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49247604:49247604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5420A>T
AA Mutation	p.Gln1807Leu(p.Q1807L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49252827:49252827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746301877
CDS Mutation	c.3109C>T
AA Mutation	p.Arg1037Cys(p.R1037C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49270586:49270586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409Gln(p.R409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49270376:49270376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770833497
CDS Mutation	c.1436G>A
AA Mutation	p.Arg479Gln(p.R479Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49247313:49247313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767986153
CDS Mutation	c.5711C>T
AA Mutation	p.Thr1904Met(p.T1904M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49248475:49248475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377375503
CDS Mutation	c.4549C>T
AA Mutation	p.Arg1517Cys(p.R1517C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49248381:49248381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4643A>G
AA Mutation	p.His1548Arg(p.H1548R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49247958:49247958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5066T>C
AA Mutation	p.Leu1689Pro(p.L1689P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49249627:49249627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3397G>C
AA Mutation	p.Glu1133Gln(p.E1133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49247622:49247622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5402T>G
AA Mutation	p.Phe1801Cys(p.F1801C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49257575:49257575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2506C>G
AA Mutation	p.Arg836Gly(p.R836G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49249141:49249141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765271746
CDS Mutation	c.3883C>T
AA Mutation	p.Arg1295Cys(p.R1295C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49249318:49249318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3706A>G
AA Mutation	p.Met1236Val(p.M1236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49254584:49254584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562054265
CDS Mutation	c.2870G>A
AA Mutation	p.Arg957His(p.R957H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49271210:49271210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778680326
CDS Mutation	c.602G>A
AA Mutation	p.Arg201His(p.R201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49260531:49260531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348T>C
AA Mutation	p.Leu783Pro(p.L783P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49248171:49248171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4853T>G
AA Mutation	p.Val1618Gly(p.V1618G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49248762:49248762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4262G>A
AA Mutation	p.Gly1421Asp(p.G1421D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49271244:49271244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>A
AA Mutation	p.Val190Ile(p.V190I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49270265:49270265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547G>T
AA Mutation	p.Arg516Met(p.R516M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49270804:49270804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008G>A
AA Mutation	p.Met336Ile(p.M336I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49248308:49248308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4716A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49264803:49264803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2064C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49248025:49248025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49247450:49247450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181876800
CDS Mutation	c.5574C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49249526:49249526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34059789
CDS Mutation	c.3498C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49247312:49247312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760033410
CDS Mutation	c.5712G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49247420:49247420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116689515
CDS Mutation	c.5604G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49271614:49271614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371752
Start	49255914:49255914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2698delA
AA Mutation	p.Arg900GlufsTer2(p.R900Efs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000371752
Start	49254643:49254643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2811G>A
AA Mutation	p.Trp937Ter(p.W937*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000371752
Start	49271103:49271103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772546721
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Ter(p.R237*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371752
Start	49270153:49270154(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1658dupG
AA Mutation	p.Arg554GlnfsTer30(p.R554Qfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000371752
Start	49247963:49247965(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759078873
CDS Mutation	c.5059_5061delGAG
AA Mutation	p.Glu1687del(p.E1687del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNFX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49249630:49249630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3394C>T
AA Mutation	p.His1132Tyr(p.H1132Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49271325:49271325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487A>C
AA Mutation	p.Thr163Pro(p.T163P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49257472:49257472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2609A>C
AA Mutation	p.Asp870Ala(p.D870A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49257554:49257554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2527G>A
AA Mutation	p.Val843Met(p.V843M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49247621:49247621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5403C>A
AA Mutation	p.Phe1801Leu(p.F1801L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49255896:49255896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553344985
CDS Mutation	c.2716C>T
AA Mutation	p.Arg906Cys(p.R906C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49266149:49266149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988A>G
AA Mutation	p.Asp663Gly(p.D663G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49271238:49271238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769208606
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Trp(p.R192W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371752
Start	49264832:49264832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2035C>T
AA Mutation	p.Arg679Trp(p.R679W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49249304:49249304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3720G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49249643:49249643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371752
Start	49264803:49264803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2064C>T
Mutation Classification	Silent
Feature Type	Transcript