Primary Site >> Stomach Cancer

Gene >> CDCP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000296129
Start 45095431:45095431(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1162A>G
AA Mutation p.Thr388Ala(p.T388A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000296129
Start 45110607:45110607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751386844
CDS Mutation c.890T>C
AA Mutation p.Leu297Pro(p.L297P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000296129
Start 45093351:45093351(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750220191
CDS Mutation c.1553G>A
AA Mutation p.Arg518His(p.R518H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000296129
Start 45112142:45112142(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.596C>A
AA Mutation p.Pro199Gln(p.P199Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000296129
Start 45093649:45093649(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781414038
CDS Mutation c.1255G>A
AA Mutation p.Asp419Asn(p.D419N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000296129
Start 45112376:45112376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.362T>G
AA Mutation p.Leu121Arg(p.L121R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000296129
Start 45091357:45091357(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370889670
CDS Mutation c.1809C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000296129
Start 45095516:45095516(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763806182
CDS Mutation c.1077C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000296129
Start 45091300:45091300(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368493580
CDS Mutation c.1866C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000296129
Start 45112167:45112167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571G>T
AA Mutation p.Gly191Ter(p.G191*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000296129
Start 45085986:45085987(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2162dupA
AA Mutation p.Phe722ValfsTer9(p.F722Vfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript