Primary Site >> Liver Cancer

Gene >> ROR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375708
Start 91724462:91724462(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2032T>A
AA Mutation p.Tyr678Asn(p.Y678N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375708
Start 91733329:91733329(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148340413
CDS Mutation c.730C>T
AA Mutation p.Arg244Trp(p.R244W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375708
Start 91733251:91733251(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145631389
CDS Mutation c.808A>G
AA Mutation p.Ile270Val(p.I270V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000375715
Start 91694383:91694383(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2094C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000375708
Start 91730956:91730956(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767456619
CDS Mutation c.1137G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000375708
Start 91726688:91726688(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1239A>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000375708
Start 91733183:91733183(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.876T>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000375708
Start 91723926:91723926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2568C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000375708
Start 91724865:91724865(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1629G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000375708
Start 91724048:91724048(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2446C>T
AA Mutation p.Gln816Ter(p.Q816*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript