Colon Cancer: Gene >> BCORL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130014266:130014266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1494G>T
AA Mutation	p.Glu498Asp(p.E498D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015971:130015971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373106469
CDS Mutation	c.3199C>T
AA Mutation	p.Arg1067Trp(p.R1067W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130012607:130012607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199910278
CDS Mutation	c.116C>T
AA Mutation	p.Thr39Met(p.T39M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130025247:130025247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3946G>A
AA Mutation	p.Glu1316Lys(p.E1316K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130037518:130037518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4457C>T
AA Mutation	p.Ala1486Val(p.A1486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130014723:130014723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1951C>G
AA Mutation	p.His651Asp(p.H651D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130005286:130005286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Trp(p.R19W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130050781:130050781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4683C>A
AA Mutation	p.Ser1561Arg(p.S1561R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130016194:130016194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3422G>A
AA Mutation	p.Arg1141Gln(p.R1141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015925:130015925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3153G>T
AA Mutation	p.Met1051Ile(p.M1051I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130025098:130025098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537443044
CDS Mutation	c.3797G>A
AA Mutation	p.Arg1266Gln(p.R1266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130013539:130013539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368979206
CDS Mutation	c.767C>T
AA Mutation	p.Pro256Leu(p.P256L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130014660:130014660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1888C>T
AA Mutation	p.Arg630Cys(p.R630C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015749:130015749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2977C>T
AA Mutation	p.His993Tyr(p.H993Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130015196:130015196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138691600
CDS Mutation	c.2424G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130014662:130014662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130014512:130014512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746346454
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130028747:130028747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760649587
CDS Mutation	c.4191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130015379:130015379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2607T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130013075:130013075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374936854
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130015373:130015373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147051252
CDS Mutation	c.2601G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130012614:130012614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130025264:130025264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3963A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130055893:130055893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4893G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130013162:130013162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749788362
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130056036:130056036(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778658185
CDS Mutation	c.5042delC
AA Mutation	p.Pro1681GlnfsTer20(p.P1681Qfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130021034:130021034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3496delG
AA Mutation	p.Ala1166LeufsTer56(p.A1166Lfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130013374:130013374(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.605delC
AA Mutation	p.Pro202LeufsTer51(p.P202Lfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130028726:130028726(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4173delG
AA Mutation	p.Ile1392SerfsTer58(p.I1392Sfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000218147
Start	130016163:130016163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3391C>T
AA Mutation	p.Gln1131Ter(p.Q1131*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000218147
Start	130015122:130015122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2350C>T
AA Mutation	p.Arg784Ter(p.R784*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130013735:130013736(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.968dupC
AA Mutation	p.Ser324PhefsTer96(p.S324Ffs*96)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCORL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130039154:130039154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4490T>G
AA Mutation	p.Val1497Gly(p.V1497G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130015559:130015559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2787G>T
AA Mutation	p.Gln929His(p.Q929H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000218147
Start	130016041:130016041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3269G>A
AA Mutation	p.Arg1090Gln(p.R1090Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130014185:130014185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1413G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000218147
Start	130021002:130021002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3459T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000218147
Start	130056036:130056036(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778658185
CDS Mutation	c.5042delC
AA Mutation	p.Pro1681GlnfsTer20(p.P1681Qfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000218147
Start	130016040:130016040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3268C>T
AA Mutation	p.Arg1090Ter(p.R1090*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript