Colon Cancer: Gene >> ADGRL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14156962:14156962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2944G>A
AA Mutation	p.Ala982Thr(p.A982T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162756:14162756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144793304
CDS Mutation	c.1060C>T
AA Mutation	p.Arg354Cys(p.R354C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14155379:14155379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3289C>T
AA Mutation	p.His1097Tyr(p.H1097Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14151418:14151418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3880C>G
AA Mutation	p.Arg1294Gly(p.R1294G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14163233:14163233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765304593
CDS Mutation	c.583G>A
AA Mutation	p.Asp195Asn(p.D195N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14163014:14163014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802A>G
AA Mutation	p.Ile268Val(p.I268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14163127:14163127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689C>T
AA Mutation	p.Thr230Met(p.T230M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14161383:14161383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1454T>C
AA Mutation	p.Val485Ala(p.V485A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14160279:14160279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>A
AA Mutation	p.Ala550Thr(p.A550T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14156985:14156985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2921C>T
AA Mutation	p.Pro974Leu(p.P974L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14160152:14160152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372129747
CDS Mutation	c.1775G>A
AA Mutation	p.Arg592Gln(p.R592Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14163149:14163149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754888851
CDS Mutation	c.667G>A
AA Mutation	p.Val223Ile(p.V223I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14157432:14157432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2579T>G
AA Mutation	p.Leu860Arg(p.L860R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14161504:14161504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1333G>C
AA Mutation	p.Gly445Arg(p.G445R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14161462:14161462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375G>A
AA Mutation	p.Ala459Thr(p.A459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14151328:14151328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781735623
CDS Mutation	c.3970G>A
AA Mutation	p.Gly1324Arg(p.G1324R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162692:14162692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124A>T
AA Mutation	p.Asn375Ile(p.N375I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14151037:14151037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764585021
CDS Mutation	c.4261G>A
AA Mutation	p.Glu1421Lys(p.E1421K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162825:14162825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991G>A
AA Mutation	p.Val331Met(p.V331M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14150968:14150968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754657629
CDS Mutation	c.4330C>T
AA Mutation	p.Arg1444Trp(p.R1444W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14160153:14160153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774C>T
AA Mutation	p.Arg592Trp(p.R592W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162982:14162982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834G>T
AA Mutation	p.Trp278Cys(p.W278C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162998:14162998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818A>G
AA Mutation	p.Asp273Gly(p.D273G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14155409:14155409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576856623
CDS Mutation	c.3259G>A
AA Mutation	p.Ala1087Thr(p.A1087T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14162763:14162763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14162703:14162703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267605305
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14161418:14161418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759880611
CDS Mutation	c.1419C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14162787:14162787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14159178:14159178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371801061
CDS Mutation	c.2076G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14163159:14163159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370076118
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340736
Start	14159159:14159159(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2095delC
AA Mutation	p.Gln699ArgfsTer47(p.Q699Rfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162879:14162879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Cys(p.R313C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000340736
Start	14159764:14159764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1825C>T
AA Mutation	p.Arg609Ter(p.R609*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340736
Start	14151525:14151526(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3772dupG
AA Mutation	p.Asp1258GlyfsTer10(p.D1258Gfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript