Mutation

Primary Site >> Liver Cancer

Gene >> EPHA3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89431336:89431336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2323C>T
AA Mutation	p.Pro775Ser(p.P775S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89210169:89210169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.463A>T
AA Mutation	p.Met155Leu(p.M155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89107833:89107833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Glu29Lys(p.E29K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89407338:89407338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1664T>A
AA Mutation	p.Leu555His(p.L555H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89342061:89342061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1277C>T
AA Mutation	p.Ala426Val(p.A426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89431231:89431231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762621864
CDS Mutation	c.2218A>T
AA Mutation	p.Met740Leu(p.M740L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89342040:89342040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256G>T
AA Mutation	p.Ser419Ile(p.S419I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89107794:89107794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46C>G
AA Mutation	p.Leu16Val(p.L16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89429109:89429109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078A>G
AA Mutation	p.Lys693Arg(p.K693R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336596
Start	89107812:89107812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64C>A
AA Mutation	p.Leu22Met(p.L22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89479454:89479454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2904C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89341844:89341844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89431341:89431341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2328A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336596
Start	89210201:89210201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336596
Start	89450212:89450213(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2538dupC
AA Mutation	p.Met847HisfsTer26(p.M847Hfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript