Primary Site >> Stomach Cancer

Gene >> SP8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361443
Start 20785252:20785252(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748563164
CDS Mutation c.511G>A
AA Mutation p.Gly171Arg(p.G171R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361443
Start 20784562:20784562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201G>A
AA Mutation p.Asp401Asn(p.D401N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361443
Start 20784955:20784955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.808C>T
AA Mutation p.His270Tyr(p.H270Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361443
Start 20784639:20784639(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1124C>T
AA Mutation p.Ala375Val(p.A375V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361443
Start 20785162:20785162(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.601G>A
AA Mutation p.Glu201Lys(p.E201K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361443
Start 20784577:20784577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1186C>T
AA Mutation p.Arg396Cys(p.R396C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20784965:20784965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.798C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20785022:20785022(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.741G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20785568:20785568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.195G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20784653:20784653(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1110T>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20785187:20785187(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.576G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20785721:20785721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.42G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000361443
Start 20784650:20784650(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1113G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000361443
Start 20785046:20785046(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.717delG
AA Mutation p.Leu240SerfsTer19(p.L240Sfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript