Colon Cancer: Gene >> ADGRL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81969248:81969248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2582G>T
AA Mutation	p.Cys861Phe(p.C861F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81950392:81950392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402T>C
AA Mutation	p.Phe468Leu(p.F468L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990942:81990942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4177G>A
AA Mutation	p.Asp1393Asn(p.D1393N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81968165:81968165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776616316
CDS Mutation	c.2477A>G
AA Mutation	p.Asn826Ser(p.N826S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81969253:81969253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2587G>A
AA Mutation	p.Ala863Thr(p.A863T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81979954:81979954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3095A>G
AA Mutation	p.Asn1032Ser(p.N1032S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81985352:81985352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3493C>A
AA Mutation	p.Gln1165Lys(p.Q1165K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990896:81990896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4131T>A
AA Mutation	p.Asn1377Lys(p.N1377K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990961:81990961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4196G>C
AA Mutation	p.Arg1399Thr(p.R1399T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81981824:81981824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3118G>A
AA Mutation	p.Ala1040Thr(p.A1040T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990981:81990981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4216T>C
AA Mutation	p.Tyr1406His(p.Y1406H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943497:81943497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926G>A
AA Mutation	p.Arg309His(p.R309H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990446:81990446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3681T>G
AA Mutation	p.Asn1227Lys(p.N1227K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943600:81943600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552007701
CDS Mutation	c.1029T>G
AA Mutation	p.Ile343Met(p.I343M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81981836:81981836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3130C>A
AA Mutation	p.Leu1044Met(p.L1044M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943554:81943554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983A>G
AA Mutation	p.Tyr328Cys(p.Y328C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81950258:81950258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758616029
CDS Mutation	c.1268C>T
AA Mutation	p.Thr423Ile(p.T423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943713:81943713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142A>G
AA Mutation	p.Asn381Ser(p.N381S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990991:81990991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4226G>T
AA Mutation	p.Ser1409Ile(p.S1409I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81966153:81966153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101G>T
AA Mutation	p.Ala701Ser(p.A701S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81837016:81837016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32T>C
AA Mutation	p.Leu11Pro(p.L11P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81950342:81950342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352C>A
AA Mutation	p.Ser451Tyr(p.S451Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943157:81943157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Cys(p.R196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943461:81943461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746200328
CDS Mutation	c.890G>A
AA Mutation	p.Arg297Gln(p.R297Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81968183:81968183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2495C>T
AA Mutation	p.Ala832Val(p.A832V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81984697:81984697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3385T>C
AA Mutation	p.Ser1129Pro(p.S1129P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943020:81943020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>G
AA Mutation	p.Tyr150Cys(p.Y150C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81952094:81952094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734G>T
AA Mutation	p.Gln578His(p.Q578H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81952042:81952042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1682C>A
AA Mutation	p.Ser561Tyr(p.S561Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81985283:81985283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3424G>T
AA Mutation	p.Asp1142Tyr(p.D1142Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81952088:81952088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728G>T
AA Mutation	p.Gln576His(p.Q576H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370717
Start	81907099:81907099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769956127
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370717
Start	81836993:81836993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370717
Start	81936746:81936746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370717
Start	81990854:81990854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4089A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370717
Start	81990743:81990743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3978A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370717
Start	81952991:81952991(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1791delA
AA Mutation	p.Lys597AsnfsTer21(p.K597Nfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000370717
Start	81951093:81951093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1568C>A
AA Mutation	p.Ser523Ter(p.S523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000370717
Start	81907055:81907055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112C>T
AA Mutation	p.Arg38Ter(p.R38*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000370717
Start	81970520:81970520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2928T>G
AA Mutation	p.Tyr976Ter(p.Y976*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000370717
Start	81986939:81986939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754660598
CDS Mutation	c.3535C>T
AA Mutation	p.Arg1179Ter(p.R1179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370717
Start	81969276:81969277(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2615dupT
AA Mutation	p.Arg873ProfsTer6(p.R873Pfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370717
Start	81990701:81990702(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3938dupA
AA Mutation	p.Asn1313LysfsTer37(p.N1313Kfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370717
Start	81966592:81966593(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2323dupC
AA Mutation	p.Leu775ProfsTer5(p.L775Pfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370717
Start	81943296:81943297(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.725_726insCTATTTT
AA Mutation	p.Glu242AspfsTer7(p.E242Dfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81981908:81981908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3202C>T
AA Mutation	p.Leu1068Phe(p.L1068F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990959:81990959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4194G>C
AA Mutation	p.Arg1398Ser(p.R1398S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81986955:81986955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3551A>G
AA Mutation	p.Asn1184Ser(p.N1184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943106:81943106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752679138
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Cys(p.R179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81991002:81991002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4237C>A
AA Mutation	p.Leu1413Ile(p.L1413I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81943230:81943230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659T>C
AA Mutation	p.Phe220Ser(p.F220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81936754:81936754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314T>C
AA Mutation	p.Val105Ala(p.V105A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81970455:81970455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756113269
CDS Mutation	c.2863G>A
AA Mutation	p.Val955Ile(p.V955I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370717
Start	81990424:81990424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3659C>G
AA Mutation	p.Ala1220Gly(p.A1220G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370717
Start	81979913:81979913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749616854
CDS Mutation	c.3054G>A
Mutation Classification	Silent
Feature Type	Transcript