Primary Site >> Stomach Cancer

Gene >> PTK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140735326:140735326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1955A>G
AA Mutation p.Tyr652Cys(p.Y652C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140879577:140879577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.256C>T
AA Mutation p.Arg86Cys(p.R86C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140735392:140735392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1889A>G
AA Mutation p.Asp630Gly(p.D630G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140752300:140752300(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778100779
CDS Mutation c.1349C>T
AA Mutation p.Ala450Val(p.A450V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140818321:140818321(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.823G>T
AA Mutation p.Gly275Cys(p.G275C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140735266:140735266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2015T>C
AA Mutation p.Leu672Pro(p.L672P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000521059
Start 140700920:140700920(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150410292
CDS Mutation c.2470C>T
AA Mutation p.Arg824Cys(p.R824C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000521059
Start 140717703:140717703(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2037C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000521059
Start 140735313:140735313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776101894
CDS Mutation c.1968G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000521059
Start 140668326:140668326(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141828978
CDS Mutation c.2808C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000521059
Start 140717604:140717604(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759165150
CDS Mutation c.2136G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000521059
Start 140702687:140702687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2250A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000521059
Start 140793374:140793374(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1104G>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000521059
Start 140803560:140803560(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.958delA
AA Mutation p.Ile320Ter(p.I320*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000521059
Start 140743260:140743260(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1705C>T
AA Mutation p.Arg569Ter(p.R569*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000521059
Start 140739054:140739054(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1789C>T
AA Mutation p.Arg597Ter(p.R597*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000521059
Start 140890608:140890609(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.129dupT
AA Mutation p.Glu44Ter(p.E44*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 18
Mutation Consequence splice_donor_variant
Transcription ID ENST00000521059
Start 140761163:140761163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1332+2T>C
Mutation Classification Splice_Site
Feature Type Transcript