Colon Cancer: Gene >> EPHA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133498:16133498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1847A>G
AA Mutation	p.Gln616Arg(p.Q616R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16135123:16135123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1495C>A
AA Mutation	p.Pro499Thr(p.P499T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16134543:16134543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755908156
CDS Mutation	c.1607C>T
AA Mutation	p.Ala536Val(p.A536V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16137857:16137857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308G>C
AA Mutation	p.Gln436His(p.Q436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133293:16133293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776917686
CDS Mutation	c.1940C>T
AA Mutation	p.Thr647Met(p.T647M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16138394:16138394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860A>G
AA Mutation	p.Glu287Gly(p.E287G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16137937:16137937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228T>A
AA Mutation	p.Phe410Ile(p.F410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16133233:16133233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2000T>C
AA Mutation	p.Met667Thr(p.M667T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358432
Start	16131839:16131839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2357C>T
AA Mutation	p.Pro786Leu(p.P786L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16135055:16135055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1563G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16135730:16135730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372348376
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16148748:16148748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139200871
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16138333:16138333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775233932
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16148439:16148439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16150908:16150908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370213656
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16132262:16132262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140708366
CDS Mutation	c.2127C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358432
Start	16135700:16135700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143181899
CDS Mutation	c.1383G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16148482:16148482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.719delG
AA Mutation	p.Gly240ValfsTer153(p.G240Vfs*153)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16135704:16135704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1379delC
AA Mutation	p.Pro460ArgfsTer33(p.P460Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16135069:16135069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1549delG
AA Mutation	p.Ala517ProfsTer21(p.A517Pfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358432
Start	16148481:16148482(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.719dupG
AA Mutation	p.Glu241Ter(p.E241*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EPHA2

No Mutation Annotation!