Primary Site >> Stomach Cancer

Gene >> UNC5CL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000244565
Start 41034098:41034098(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.469C>G
AA Mutation p.Gln157Glu(p.Q157E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000244565
Start 41028450:41028450(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1480A>T
AA Mutation p.Thr494Ser(p.T494S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000244565
Start 41034764:41034764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.311C>T
AA Mutation p.Ser104Leu(p.S104L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000244565
Start 41028533:41028533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1397G>A
AA Mutation p.Gly466Asp(p.G466D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000244565
Start 41033109:41033109(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773255844
CDS Mutation c.724G>A
AA Mutation p.Glu242Lys(p.E242K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000244565
Start 41028520:41028520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778438173
CDS Mutation c.1410G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000244565
Start 41030675:41030675(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1200C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000244565
Start 41034900:41034900(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs748733935
CDS Mutation c.175delC
AA Mutation p.Gln59AsnfsTer2(p.Q59Nfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000244565
Start 41030664:41030664(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1211delC
AA Mutation p.Pro404HisfsTer39(p.P404Hfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000244565
Start 41028525:41028525(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1405C>T
AA Mutation p.Gln469Ter(p.Q469*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000244565
Start 41034055:41034056(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.511dupG
AA Mutation p.Ala171GlyfsTer50(p.A171Gfs*50)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript