Primary Site >> Stomach Cancer

Gene >> DAND5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000317060
Start 12973605:12973605(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373817477
CDS Mutation c.541G>A
AA Mutation p.Glu181Lys(p.E181K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000317060
Start 12969721:12969721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61T>C
AA Mutation p.Ser21Pro(p.S21P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000317060
Start 12973404:12973404(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765612939
CDS Mutation c.340G>A
AA Mutation p.Gly114Ser(p.G114S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000317060
Start 12973589:12973589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.525A>G
AA Mutation p.Ile175Met(p.I175M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000317060
Start 12973568:12973568(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.504C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000317060
Start 12973454:12973454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.390C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000317060
Start 12969795:12969795(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.135A>G
Mutation Classification Silent
Feature Type Transcript