Colon Cancer: Gene >> EPHA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22593558:22593558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1475C>T
AA Mutation	p.Ala492Val(p.A492V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22597780:22597780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557674245
CDS Mutation	c.2035C>T
AA Mutation	p.Arg679Trp(p.R679W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22600926:22600926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149877319
CDS Mutation	c.2567G>A
AA Mutation	p.Arg856His(p.R856H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22601424:22601424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746166476
CDS Mutation	c.2854G>A
AA Mutation	p.Ala952Thr(p.A952T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576569:22576569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776511588
CDS Mutation	c.512G>A
AA Mutation	p.Arg171His(p.R171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22597769:22597769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2024A>G
AA Mutation	p.Glu675Gly(p.E675G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22601433:22601433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2863G>A
AA Mutation	p.Gly955Arg(p.G955R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576713:22576713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Met(p.T219M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22597727:22597727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1982A>G
AA Mutation	p.Asp661Gly(p.D661G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576843:22576843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786C>G
AA Mutation	p.Cys262Trp(p.C262W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22599007:22599007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750373572
CDS Mutation	c.2348G>A
AA Mutation	p.Arg783Gln(p.R783Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576373:22576373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576336:22576336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576837:22576837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749326341
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576726:22576726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22576588:22576588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000166244
Start	22569332:22569332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138G>A
AA Mutation	p.Trp46Ter(p.W46*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EPHA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22588961:22588961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070G>T
AA Mutation	p.Arg357Leu(p.R357L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22601319:22601319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147795823
CDS Mutation	c.2749G>A
AA Mutation	p.Val917Ile(p.V917I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000166244
Start	22576374:22576374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317G>A
AA Mutation	p.Arg106His(p.R106H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000166244
Start	22595279:22595279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653C>A
Mutation Classification	Silent
Feature Type	Transcript