Primary Site >> Stomach Cancer

Gene >> NOC2L

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000327044
Start 954071:954071(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150111944
CDS Mutation c.710C>T
AA Mutation p.Pro237Leu(p.P237L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000327044
Start 952474:952474(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372047419
CDS Mutation c.1129G>A
AA Mutation p.Ala377Thr(p.A377T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000327044
Start 948516:948516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1531G>A
AA Mutation p.Val511Ile(p.V511I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000327044
Start 953846:953846(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554175821
CDS Mutation c.824G>A
AA Mutation p.Arg275Gln(p.R275Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000327044
Start 956211:956211(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138672231
CDS Mutation c.491G>A
AA Mutation p.Arg164His(p.R164H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000327044
Start 948497:948497(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375064108
CDS Mutation c.1550C>T
AA Mutation p.Ala517Val(p.A517V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000327044
Start 953866:953866(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754350344
CDS Mutation c.804G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000327044
Start 956204:956204(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.498T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000327044
Start 951181:951181(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759947913
CDS Mutation c.1389G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000327044
Start 956942:956942(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438T>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000327044
Start 954049:954049(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.732delG
AA Mutation p.Lys245SerfsTer41(p.K245Sfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000327044
Start 946494:946494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1711C>T
AA Mutation p.Gln571Ter(p.Q571*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence start_lost
Transcription ID ENST00000327044
Start 959239:959239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2T>C
AA Mutation p.Met1?(p.M1?)
Mutation Classification Translation_Start_Site
Feature Type Transcript