Primary Site >> Stomach Cancer

Gene >> POLA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379059
Start 24732448:24732448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1747T>C
AA Mutation p.Phe583Leu(p.F583L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379059
Start 24815014:24815014(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3314G>A
AA Mutation p.Arg1105Gln(p.R1105Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379059
Start 24714572:24714572(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748968830
CDS Mutation c.347G>A
AA Mutation p.Arg116His(p.R116H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379059
Start 24888043:24888043(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4067G>A
AA Mutation p.Arg1356Gln(p.R1356Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379059
Start 24741428:24741428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2252T>C
AA Mutation p.Phe751Ser(p.F751S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379059
Start 24724426:24724426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1274A>G
AA Mutation p.Tyr425Cys(p.Y425C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000379059
Start 24716453:24716453(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200756660
CDS Mutation c.599C>T
AA Mutation p.Thr200Met(p.T200M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000379059
Start 24727831:24727831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1563G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000379059
Start 24742047:24742047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2374T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000379059
Start 24739407:24739407(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2055C>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000379059
Start 24716894:24716894(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.611C>A
AA Mutation p.Ser204Ter(p.S204*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000379059
Start 24739511:24739512(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2159_2160insAGCAGACACT
AA Mutation p.Val721AlafsTer17(p.V721Afs*17)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000379059
Start 24812735:24812736(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3158dupA
AA Mutation p.Lys1054GlufsTer8(p.K1054Efs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript