Primary Site >> Stomach Cancer

Gene >> BTK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308731
Start 101353322:101353322(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1780G>T
AA Mutation p.Gly594Trp(p.G594W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308731
Start 101353222:101353222(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1880A>G
AA Mutation p.Tyr627Cys(p.Y627C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308731
Start 101375245:101375245(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.40T>A
AA Mutation p.Ser14Thr(p.S14T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000308731
Start 101358419:101358419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.993A>G
AA Mutation p.Ile331Met(p.I331M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000308731
Start 101358631:101358631(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.960T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000308731
Start 101374578:101374578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.198A>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000308731
Start 101362203:101362203(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.558G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000308731
Start 101370053:101370053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.336C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000308731
Start 101362599:101362599(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.482delA
AA Mutation p.Asn161MetfsTer15(p.N161Mfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript