Primary Site >> Stomach Cancer

Gene >> SCIN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12622805:12622805(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.671T>C
AA Mutation p.Leu224Ser(p.L224S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12640440:12640440(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1504G>A
AA Mutation p.Gly502Arg(p.G502R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12629108:12629108(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375869092
CDS Mutation c.1205G>A
AA Mutation p.Arg402His(p.R402H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12652591:12652591(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2024A>C
AA Mutation p.Lys675Thr(p.K675T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000297029
Start 12636135:12636135(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1410G>T
AA Mutation p.Gln470His(p.Q470H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12629171:12629171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1268A>G
AA Mutation p.Asp423Gly(p.D423G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000297029
Start 12644170:12644170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371472039
CDS Mutation c.1614C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000297029
Start 12622827:12622827(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.693A>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000297029
Start 12640458:12640458(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1526delC
AA Mutation p.Pro509LeufsTer27(p.P509Lfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000297029
Start 12640432:12640432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1496C>G
AA Mutation p.Ser499Ter(p.S499*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000297029
Start 12644609:12644610(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1791dupA
AA Mutation p.Asp598ArgfsTer13(p.D598Rfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript