Colon Cancer: Gene >> ROBO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124891431:124891431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749338809
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Cys(p.R606C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124887774:124887774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2015A>G
AA Mutation	p.Glu672Gly(p.E672G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124894001:124894001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1363C>T
AA Mutation	p.Pro455Ser(p.P455S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124896257:124896257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620G>T
AA Mutation	p.Cys207Phe(p.C207F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124887476:124887476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776188598
CDS Mutation	c.2080G>A
AA Mutation	p.Ala694Thr(p.A694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124894294:124894294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372037630
CDS Mutation	c.1225G>A
AA Mutation	p.Ala409Thr(p.A409T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124893965:124893965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201893985
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Trp(p.R467W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124897030:124897030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302A>G
AA Mutation	p.Asp101Gly(p.D101G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124894276:124894276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243T>G
AA Mutation	p.Ser415Ala(p.S415A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124886761:124886761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138244465
CDS Mutation	c.2497G>A
AA Mutation	p.Val833Ile(p.V833I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124887085:124887085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144947842
CDS Mutation	c.2327G>A
AA Mutation	p.Arg776His(p.R776H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124894293:124894293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226C>T
AA Mutation	p.Ala409Val(p.A409V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124893887:124893887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755801141
CDS Mutation	c.1477C>T
AA Mutation	p.Arg493Cys(p.R493C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124894268:124894268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124894211:124894211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124886474:124886474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754985662
CDS Mutation	c.2784C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124886762:124886762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771809588
CDS Mutation	c.2496C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124895896:124895896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200292596
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124897739:124897739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124897007:124897007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143490922
CDS Mutation	c.325C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306534
Start	124897764:124897764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781111238
CDS Mutation	c.32delG
AA Mutation	p.Gly11AlafsTer25(p.G11Afs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000306534
Start	124895568:124895568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925G>T
AA Mutation	p.Glu309Ter(p.E309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ROBO4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124886646:124886646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2612G>C
AA Mutation	p.Gly871Ala(p.G871A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124896634:124896634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748069633
CDS Mutation	c.437T>C
AA Mutation	p.Met146Thr(p.M146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306534
Start	124886553:124886553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2705C>T
AA Mutation	p.Ala902Val(p.A902V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124887755:124887755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2034C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124894295:124894295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747419484
CDS Mutation	c.1224C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124891558:124891558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1689C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306534
Start	124897041:124897041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000306534
Start	124896614:124896614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457C>T
AA Mutation	p.Gln153Ter(p.Q153*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript