Primary Site >> Stomach Cancer

Gene >> RIN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66334888:66334888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.911G>A
AA Mutation p.Ser304Asn(p.S304N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66332530:66332530(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs11227461
CDS Mutation c.2098G>A
AA Mutation p.Val700Ile(p.V700I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66332292:66332292(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757397798
CDS Mutation c.2336G>A
AA Mutation p.Arg779Gln(p.R779Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66333641:66333641(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145559573
CDS Mutation c.1609G>A
AA Mutation p.Asp537Asn(p.D537N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66335057:66335057(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141887009
CDS Mutation c.742C>T
AA Mutation p.Arg248Cys(p.R248C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66332293:66332293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144651587
CDS Mutation c.2335C>T
AA Mutation p.Arg779Trp(p.R779W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000311320
Start 66334994:66334994(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141270180
CDS Mutation c.805G>A
AA Mutation p.Val269Met(p.V269M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000311320
Start 66334830:66334830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.969G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000311320
Start 66332702:66332702(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1926G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000311320
Start 66335982:66335982(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.263delC
AA Mutation p.Pro88ArgfsTer54(p.P88Rfs*54)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000311320
Start 66335001:66335001(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.798delC
AA Mutation p.Val267SerfsTer84(p.V267Sfs*84)
Mutation Classification Frame_Shift_Del
Feature Type Transcript