Colon Cancer: Gene >> EPHB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22863078:22863078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22865084:22865084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777940741
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392His(p.R392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22910514:22910514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767807199
CDS Mutation	c.2635A>G
AA Mutation	p.Thr879Ala(p.T879A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22882448:22882448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371215652
CDS Mutation	c.1393G>A
AA Mutation	p.Val465Met(p.V465M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22913532:22913532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372681830
CDS Mutation	c.2923C>T
AA Mutation	p.Arg975Trp(p.R975W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22784947:22784947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755610456
CDS Mutation	c.682G>A
AA Mutation	p.Ala228Thr(p.A228T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22882475:22882475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420T>C
AA Mutation	p.Tyr474His(p.Y474H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22906040:22906040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1819G>A
AA Mutation	p.Glu607Lys(p.E607K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22910559:22910559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2680G>A
AA Mutation	p.Ala894Thr(p.A894T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22909091:22909091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2422G>A
AA Mutation	p.Asp808Asn(p.D808N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22892959:22892959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777155810
CDS Mutation	c.1504G>A
AA Mutation	p.Ala502Thr(p.A502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22909083:22909083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2414C>T
AA Mutation	p.Ser805Leu(p.S805L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22781450:22781450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141486320
CDS Mutation	c.91G>A
AA Mutation	p.Ala31Thr(p.A31T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400191
Start	22864887:22864887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400191
Start	22906918:22906918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538962894
CDS Mutation	c.2097C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400191
Start	22906102:22906102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371734479
CDS Mutation	c.1881C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400191
Start	22906744:22906744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1923G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400191
Start	22784997:22784997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761772326
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400191
Start	22913753:22913753(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs563863657
CDS Mutation	c.3059delA
AA Mutation	p.Lys1020ArgfsTer63(p.K1020Rfs*63)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000400191
Start	22896480:22896480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1765+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> EPHB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400191
Start	22892993:22892993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1538T>G
AA Mutation	p.Val513Gly(p.V513G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript