Primary Site >> Stomach Cancer

Gene >> PIGR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356495
Start 206935804:206935804(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760283428
CDS Mutation c.1060C>T
AA Mutation p.Arg354Cys(p.R354C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356495
Start 206937700:206937700(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763319879
CDS Mutation c.440C>T
AA Mutation p.Thr147Met(p.T147M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356495
Start 206931760:206931760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2051C>T
AA Mutation p.Ser684Leu(p.S684L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356495
Start 206933145:206933145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773604801
CDS Mutation c.1727C>T
AA Mutation p.Ala576Val(p.A576V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000356495
Start 206930364:206930364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2249C>T
AA Mutation p.Ser750Phe(p.S750F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000356495
Start 206939192:206939192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376707589
CDS Mutation c.315C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000356495
Start 206933126:206933126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1746T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000356495
Start 206934595:206934595(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764167496
CDS Mutation c.1530C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206937333:206937333(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.807delT
AA Mutation p.Leu270CysfsTer42(p.L270Cfs*42)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000356495
Start 206939278:206939278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.229A>T
AA Mutation p.Lys77Ter(p.K77*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000356495
Start 206931680:206931680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2131G>T
AA Mutation p.Gly711Ter(p.G711*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000356495
Start 206934615:206934615(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1510C>T
AA Mutation p.Gln504Ter(p.Q504*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206932489:206932490(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1973_1974dupTG
AA Mutation p.Gly659TrpfsTer172(p.G659Wfs*172)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206935784:206935785(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1079dupA
AA Mutation p.Val362GlyfsTer15(p.V362Gfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206934564:206934565(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1560dupT
AA Mutation p.Asp521Ter(p.D521*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206937131:206937132(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1008dupC
AA Mutation p.Ser337LeufsTer12(p.S337Lfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206939368:206939369(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.138dupT
AA Mutation p.Val47CysfsTer15(p.V47Cfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000356495
Start 206934666:206934667(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1458dupC
AA Mutation p.Lys487GlnfsTer14(p.K487Qfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript