Colon Cancer: Gene >> EPHB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184581341:184581341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2821C>T
AA Mutation	p.Arg941Trp(p.R941W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184581015:184581015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2582T>C
AA Mutation	p.Met861Thr(p.M861T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184580841:184580841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759032023
CDS Mutation	c.2501A>G
AA Mutation	p.Tyr834Cys(p.Y834C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184577085:184577085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763505156
CDS Mutation	c.1256C>T
AA Mutation	p.Thr419Met(p.T419M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184580513:184580513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2284C>T
AA Mutation	p.Arg762Cys(p.R762C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184573096:184573096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776A>G
AA Mutation	p.Asp259Gly(p.D259G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184578424:184578424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1759C>T
AA Mutation	p.His587Tyr(p.H587Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184577423:184577423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564635010
CDS Mutation	c.1435C>T
AA Mutation	p.Pro479Ser(p.P479S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184579778:184579778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2016C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184572806:184572806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756886601
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184575858:184575858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184581154:184581154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551443278
CDS Mutation	c.2721C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184580440:184580440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2211C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184580857:184580857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2517C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330394
Start	184579514:184579514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1839C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000330394
Start	184577703:184577703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1525C>T
AA Mutation	p.Gln509Ter(p.Q509*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330394
Start	184581064:184581065(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2631_2632insACTGCTGGGTGTGT
AA Mutation	p.Asp878ThrfsTer88(p.D878Tfs*88)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330394
Start	184581384:184581385(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2866dupC
AA Mutation	p.Leu956ProfsTer228(p.L956Pfs*228)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EPHB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184577001:184577001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141064214
CDS Mutation	c.1172G>A
AA Mutation	p.Arg391His(p.R391H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330394
Start	184572630:184572630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745841437
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Trp(p.R104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript