Primary Site >> Stomach Cancer

Gene >> DAB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57145325:57145325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.172G>A
AA Mutation p.Asp58Asn(p.D58N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57015086:57015086(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773635680
CDS Mutation c.1340C>T
AA Mutation p.Thr447Met(p.T447M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57011148:57011148(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1668A>C
AA Mutation p.Glu556Asp(p.E556D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57010723:57010723(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1739A>G
AA Mutation p.Asp580Gly(p.D580G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57069419:57069419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.604G>A
AA Mutation p.Val202Met(p.V202M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57015339:57015339(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199793708
CDS Mutation c.1087G>A
AA Mutation p.Ala363Thr(p.A363T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57069392:57069392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.631C>T
AA Mutation p.Arg211Cys(p.R211C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57136626:57136626(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151141316
CDS Mutation c.223G>A
AA Mutation p.Ala75Thr(p.A75T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57136631:57136631(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.218C>A
AA Mutation p.Ala73Asp(p.A73D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57033412:57033412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.796T>C
AA Mutation p.Phe266Leu(p.F266L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000371231
Start 57071616:57071616(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.464G>A
AA Mutation p.Arg155Lys(p.R155K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000371231
Start 57062945:57062945(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.664-2A>G
Mutation Classification Splice_Site
Feature Type Transcript