Colon Cancer: Gene >> CASP8AP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89863675:89863675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753052099
CDS Mutation	c.1966G>A
AA Mutation	p.Glu656Lys(p.E656K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89871347:89871347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5851T>G
AA Mutation	p.Phe1951Val(p.F1951V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89863196:89863196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1487A>T
AA Mutation	p.His496Leu(p.H496L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89867929:89867929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4639C>T
AA Mutation	p.Arg1547Cys(p.R1547C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89862617:89862617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758643574
CDS Mutation	c.908C>T
AA Mutation	p.Ser303Leu(p.S303L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89868800:89868800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5510G>T
AA Mutation	p.Arg1837Ile(p.R1837I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89867257:89867257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3967C>A
AA Mutation	p.Leu1323Ile(p.L1323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89862623:89862623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914T>G
AA Mutation	p.Phe305Cys(p.F305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89868473:89868473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377357235
CDS Mutation	c.5183C>A
AA Mutation	p.Ser1728Tyr(p.S1728Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89862530:89862530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821A>G
AA Mutation	p.Glu274Gly(p.E274G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89863532:89863532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1823C>T
AA Mutation	p.Ser608Phe(p.S608F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89868940:89868940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5650G>A
AA Mutation	p.Ala1884Thr(p.A1884T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89866205:89866205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117850701
CDS Mutation	c.2915G>A
AA Mutation	p.Arg972His(p.R972H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89862659:89862659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745563258
CDS Mutation	c.950G>A
AA Mutation	p.Arg317His(p.R317H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89869013:89869013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5723C>T
AA Mutation	p.Ala1908Val(p.A1908V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89867357:89867357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4067C>T
AA Mutation	p.Ala1356Val(p.A1356V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89868593:89868593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5303A>C
AA Mutation	p.Gln1768Pro(p.Q1768P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89866876:89866876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3586T>G
AA Mutation	p.Leu1196Val(p.L1196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89869065:89869065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5775T>G
AA Mutation	p.Ile1925Met(p.I1925M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89867150:89867150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375610839
CDS Mutation	c.3860G>A
AA Mutation	p.Arg1287Gln(p.R1287Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89866204:89866204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780452119
CDS Mutation	c.2914C>T
AA Mutation	p.Arg972Cys(p.R972C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89863931:89863931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2222G>A
AA Mutation	p.Gly741Asp(p.G741D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89863599:89863599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746943629
CDS Mutation	c.1890G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89854833:89854833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89868189:89868189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4899T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89863812:89863812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89862618:89862618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377422956
CDS Mutation	c.909G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89863809:89863809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2100A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89867343:89867343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147437828
CDS Mutation	c.4053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89866605:89866605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3315T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89862730:89862730(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1026delA
AA Mutation	p.Lys342AsnfsTer2(p.K342Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89866990:89866990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3707delA
AA Mutation	p.Asn1236IlefsTer9(p.N1236Ifs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89868711:89868711(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5427delA
AA Mutation	p.Asp1810MetfsTer3(p.D1810Mfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89863510:89863510(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1804delA
AA Mutation	p.Thr602GlnfsTer8(p.T602Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000551025
Start	89863135:89863135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426G>T
AA Mutation	p.Glu476Ter(p.E476*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000551025
Start	89866099:89866099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2809G>T
AA Mutation	p.Glu937Ter(p.E937*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000551025
Start	89866417:89866417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3127C>T
AA Mutation	p.Arg1043Ter(p.R1043*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89869034:89869035(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5750dupA
AA Mutation	p.Asn1917LysfsTer4(p.N1917Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89868163:89868164(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4880_4881dupAT
AA Mutation	p.Glu1628MetfsTer58(p.E1628Mfs*58)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CASP8AP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89871318:89871318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5822G>A
AA Mutation	p.Cys1941Tyr(p.C1941Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89871293:89871293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5797G>C
AA Mutation	p.Asp1933His(p.D1933H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89862196:89862196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>T
AA Mutation	p.Asp163Tyr(p.D163Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89862617:89862617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758643574
CDS Mutation	c.908C>T
AA Mutation	p.Ser303Leu(p.S303L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89868473:89868473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377357235
CDS Mutation	c.5183C>A
AA Mutation	p.Ser1728Tyr(p.S1728Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89864113:89864113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2404C>A
AA Mutation	p.His802Asn(p.H802N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000551025
Start	89867170:89867170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771231654
CDS Mutation	c.3880G>A
AA Mutation	p.Glu1294Lys(p.E1294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89867157:89867157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141249173
CDS Mutation	c.3867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551025
Start	89869017:89869017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5727T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551025
Start	89863387:89863387(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1683delA
AA Mutation	p.Lys561AsnfsTer2(p.K561Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000551025
Start	89862148:89862148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Ter(p.R147*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript