Colon Cancer: Gene >> ADGRL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78937815:78937815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369699141
CDS Mutation	c.752C>T
AA Mutation	p.Thr251Met(p.T251M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78921650:78921650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220C>A
AA Mutation	p.Thr407Lys(p.T407K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78939202:78939202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382A>G
AA Mutation	p.Lys128Glu(p.K128E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78891641:78891641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893G>T
AA Mutation	p.Trp631Cys(p.W631C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78921734:78921734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136C>T
AA Mutation	p.Thr379Ile(p.T379I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78937963:78937963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604G>A
AA Mutation	p.Val202Ile(p.V202I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78921630:78921630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240T>G
AA Mutation	p.Ser414Ala(p.S414A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78891670:78891670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777964454
CDS Mutation	c.1864G>A
AA Mutation	p.Ala622Thr(p.A622T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78920194:78920194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1450A>C
AA Mutation	p.Asn484His(p.N484H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78917647:78917647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1736G>T
AA Mutation	p.Cys579Phe(p.C579F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78938120:78938120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>A
AA Mutation	p.Leu186Ile(p.L186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78891547:78891547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987T>G
AA Mutation	p.Phe663Val(p.F663V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78917999:78917999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1513T>C
AA Mutation	p.Phe505Leu(p.F505L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78927082:78927082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887C>A
AA Mutation	p.Ala296Glu(p.A296E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370742
Start	78917637:78917637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1746T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370742
Start	78917967:78917967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1545C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370742
Start	78920288:78920288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370742
Start	78891614:78891614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367751734
CDS Mutation	c.1920C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000370742
Start	78938243:78938243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>T
AA Mutation	p.Glu145Ter(p.E145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370742
Start	78921731:78921732(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1138_1139insGAAAAAGCAACATTTATAAATA
AA Mutation	p.Met380ArgfsTer18(p.M380Rfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78927049:78927049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920C>A
AA Mutation	p.Pro307His(p.P307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78937841:78937841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726G>T
AA Mutation	p.Lys242Asn(p.K242N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370742
Start	78939201:78939201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383A>C
AA Mutation	p.Lys128Thr(p.K128T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370742
Start	78936391:78936392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.780dupT
AA Mutation	p.Asp261Ter(p.D261*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370742
Start	78938264:78938265(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.411dupA
AA Mutation	p.Glu138ArgfsTer11(p.E138Rfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript