Primary Site >> Stomach Cancer

Gene >> SERPINA10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261994
Start 94288436:94288436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.842A>C
AA Mutation p.Lys281Thr(p.K281T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261994
Start 94290129:94290129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.465C>A
AA Mutation p.Asn155Lys(p.N155K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261994
Start 94289886:94289886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.708C>G
AA Mutation p.Ile236Met(p.I236M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261994
Start 94288457:94288457(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748068345
CDS Mutation c.821A>C
AA Mutation p.Lys274Thr(p.K274T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261994
Start 94288373:94288373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.905T>C
AA Mutation p.Leu302Pro(p.L302P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261994
Start 94290220:94290220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374A>T
AA Mutation p.Lys125Met(p.K125M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000261994
Start 94290078:94290078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.516T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000261994
Start 94288381:94288381(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.897G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000261994
Start 94284001:94284001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1299G>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000261994
Start 94288423:94288423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.855T>C
Mutation Classification Silent
Feature Type Transcript