Colon Cancer: Gene >> LY75

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159882291:159882291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113288676
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159840925:159840925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3311C>T
AA Mutation	p.Ala1104Val(p.A1104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159807098:159807098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4865T>C
AA Mutation	p.Val1622Ala(p.V1622A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159850123:159850123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3007C>T
AA Mutation	p.Leu1003Phe(p.L1003F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159879305:159879305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1469A>G
AA Mutation	p.Glu490Gly(p.E490G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159898876:159898876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278A>T
AA Mutation	p.Asn93Ile(p.N93I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159805142:159805142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5071T>C
AA Mutation	p.Phe1691Leu(p.F1691L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159842355:159842355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777959818
CDS Mutation	c.3170G>A
AA Mutation	p.Arg1057His(p.R1057H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263636
Start	159890213:159890213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802G>A
AA Mutation	p.Glu268Lys(p.E268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159878451:159878451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1647T>A
AA Mutation	p.Asp549Glu(p.D549E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159858424:159858424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2321T>G
AA Mutation	p.Phe774Cys(p.F774C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159893998:159893998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>A
AA Mutation	p.Leu185Ile(p.L185I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159898933:159898933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221G>T
AA Mutation	p.Arg74Leu(p.R74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159816961:159816961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4225A>C
AA Mutation	p.Ile1409Leu(p.I1409L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159882265:159882265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105A>T
AA Mutation	p.Asn369Tyr(p.N369Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159858416:159858416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2329T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159879268:159879268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1506T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159840747:159840747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536533438
CDS Mutation	c.3489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159850396:159850396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768079006
CDS Mutation	c.2955C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159850127:159850127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3003C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159882215:159882215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552702168
CDS Mutation	c.1155A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159875537:159875537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1881T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263636
Start	159816951:159816951(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4235delA
AA Mutation	p.Lys1412ArgfsTer2(p.K1412Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263636
Start	159840871:159840872(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs760829285
CDS Mutation	c.3364_3365delCT
AA Mutation	p.Leu1122AspfsTer6(p.L1122Dfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000263636
Start	159805100:159805100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139579850
CDS Mutation	c.5113C>T
AA Mutation	p.Arg1705Ter(p.R1705*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263636
Start	159816959:159816960(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4226_4227insAACCC
AA Mutation	p.Gln1410ThrfsTer6(p.Q1410Tfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263636
Start	159819905:159819906(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3973_3974insTCAATAACTTTAAA
AA Mutation	p.Trp1325PhefsTer24(p.W1325Ffs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000263636
Start	159882267:159882268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1102_1103insCTTACCCTC
AA Mutation	p.Asn368delinsThrTyrProHis(p.N368delinsTYPH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LY75

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263636
Start	159882210:159882210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160C>T
AA Mutation	p.Ala387Val(p.A387V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159810530:159810530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766554250
CDS Mutation	c.4695A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159819793:159819793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4086C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263636
Start	159882209:159882209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775453384
CDS Mutation	c.1161G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000263636
Start	159805100:159805100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139579850
CDS Mutation	c.5113C>T
AA Mutation	p.Arg1705Ter(p.R1705*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript