Primary Site >> Stomach Cancer

Gene >> BCL6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187726790:187726790(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147650939
CDS Mutation c.1649G>A
AA Mutation p.Arg550His(p.R550H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187729539:187729539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776120197
CDS Mutation c.866G>A
AA Mutation p.Arg289Gln(p.R289Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187722532:187722532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2047G>A
AA Mutation p.Ala683Thr(p.A683T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187729555:187729555(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.850G>A
AA Mutation p.Ala284Thr(p.A284T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187731811:187731811(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768771889
CDS Mutation c.281G>A
AA Mutation p.Arg94Gln(p.R94Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187729722:187729722(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755544927
CDS Mutation c.683G>A
AA Mutation p.Arg228Gln(p.R228Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187729282:187729282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1123T>C
AA Mutation p.Trp375Arg(p.W375R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187729261:187729261(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1144G>A
AA Mutation p.Val382Met(p.V382M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187729932:187729932(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372638471
CDS Mutation c.473G>A
AA Mutation p.Arg158Gln(p.R158Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187728524:187728524(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1376G>T
AA Mutation p.Arg459Leu(p.R459L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000232014
Start 187725006:187725006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1912C>T
AA Mutation p.Arg638Cys(p.R638C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000232014
Start 187726819:187726819(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1620C>A
Mutation Classification Silent
Feature Type Transcript