Colon Cancer: Gene >> EPHB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142866546:142866546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1528C>T
AA Mutation	p.Pro510Ser(p.P510S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142866254:142866254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181875074
CDS Mutation	c.1400T>C
AA Mutation	p.Val467Ala(p.V467A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142864513:142864513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762177890
CDS Mutation	c.713G>A
AA Mutation	p.Arg238Gln(p.R238Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142864480:142864480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680G>T
AA Mutation	p.Arg227Met(p.R227M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142870364:142870364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149014862
CDS Mutation	c.2761C>T
AA Mutation	p.Arg921Cys(p.R921C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142864422:142864422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142866056:142866056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1202A>G
AA Mutation	p.Asp401Gly(p.D401G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142864561:142864561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761C>T
AA Mutation	p.Ala254Val(p.A254V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142866526:142866526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1508A>G
AA Mutation	p.Asn503Ser(p.N503S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142868581:142868581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752688738
CDS Mutation	c.2128G>A
AA Mutation	p.Ala710Thr(p.A710T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142866040:142866040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186C>A
AA Mutation	p.Leu396Met(p.L396M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142868706:142868706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2253C>A
AA Mutation	p.Phe751Leu(p.F751L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142864089:142864089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769535474
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Trp(p.R97W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142867064:142867064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1746T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142866018:142866018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142868320:142868320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142866072:142866072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201397299
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142868733:142868733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2280C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000619012
Start	142863690:142863690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773024348
CDS Mutation	c.165+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000619012
Start	142864642:142864643(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs748119509
CDS Mutation	c.849dupC
AA Mutation	p.Arg284GlnfsTer41(p.R284Qfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000619012
Start	142870529:142870529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2805-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000619012
Start	142868050:142868050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1918+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> EPHB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142864423:142864423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142868536:142868536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56021232
CDS Mutation	c.2083C>T
AA Mutation	p.Arg695Trp(p.R695W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000619012
Start	142869845:142869845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2489C>T
AA Mutation	p.Ala830Val(p.A830V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142864538:142864538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756943658
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619012
Start	142866156:142866156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript