Colon Cancer: Gene >> E2F7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77027946:77027946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2077A>C
AA Mutation	p.Lys693Gln(p.K693Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77033950:77033950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776161589
CDS Mutation	c.1216G>T
AA Mutation	p.Ala406Ser(p.A406S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77033949:77033949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1217C>T
AA Mutation	p.Ala406Val(p.A406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77027937:77027937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2086G>A
AA Mutation	p.Glu696Lys(p.E696K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77025841:77025841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2282C>T
AA Mutation	p.Ser761Phe(p.S761F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77043089:77043089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099G>T
AA Mutation	p.Gly367Trp(p.G367W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77056100:77056100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77055923:77055923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779479853
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Trp(p.R101W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77055910:77055910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314A>G
AA Mutation	p.Lys105Arg(p.K105R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77043118:77043118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377645692
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357Gln(p.R357Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77029931:77029931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370152085
CDS Mutation	c.1784G>A
AA Mutation	p.Arg595His(p.R595H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77050644:77050644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470G>A
AA Mutation	p.Arg157His(p.R157H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77046283:77046283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584C>T
AA Mutation	p.Ser195Leu(p.S195L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77046173:77046173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694G>A
AA Mutation	p.Glu232Lys(p.E232K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77056037:77056037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187G>C
AA Mutation	p.Glu63Gln(p.E63Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77046255:77046255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612G>T
AA Mutation	p.Lys204Asn(p.K204N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77056111:77056111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149646617
CDS Mutation	c.113G>A
AA Mutation	p.Arg38Gln(p.R38Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77024151:77024151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2600G>A
AA Mutation	p.Arg867His(p.R867H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77043108:77043108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080A>C
AA Mutation	p.Lys360Asn(p.K360N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77044680:77044680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77025906:77025906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376673165
CDS Mutation	c.2217G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77028052:77028052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1971C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77024024:77024024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536978653
CDS Mutation	c.2727C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77030116:77030116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1599G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322886
Start	77055910:77055910(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.314delA
AA Mutation	p.Lys105ArgfsTer43(p.K105Rfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322886
Start	77025937:77025937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2186delC
AA Mutation	p.Pro729LeufsTer53(p.P729Lfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322886
Start	77056078:77056078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.146delA
AA Mutation	p.Asn49MetfsTer39(p.N49Mfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000322886
Start	77043191:77043191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760841332
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Ter(p.R333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000322886
Start	77025880:77025880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2243T>A
AA Mutation	p.Leu748Ter(p.L748*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000322886
Start	77030115:77030115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600G>T
AA Mutation	p.Glu534Ter(p.E534*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322886
Start	77055896:77055897(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.327_328insT
AA Mutation	p.Pro110SerfsTer3(p.P110Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000322886
Start	77033856:77033856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> E2F7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77044727:77044727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754335559
CDS Mutation	c.898G>A
AA Mutation	p.Val300Ile(p.V300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77025805:77025805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770738170
CDS Mutation	c.2318G>A
AA Mutation	p.Gly773Asp(p.G773D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322886
Start	77046060:77046060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807C>A
AA Mutation	p.Phe269Leu(p.F269L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77055879:77055879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201883014
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322886
Start	77033969:77033969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1197C>A
Mutation Classification	Silent
Feature Type	Transcript