Primary Site >> Stomach Cancer

Gene >> RALBP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9513173:9513173(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371220710
CDS Mutation c.128G>A
AA Mutation p.Arg43His(p.R43H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9517286:9517286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.686G>A
AA Mutation p.Gly229Asp(p.G229D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9522205:9522205(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.749A>G
AA Mutation p.Glu250Gly(p.E250G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9535903:9535903(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs530173610
CDS Mutation c.1934C>T
AA Mutation p.Ser645Leu(p.S645L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9535732:9535732(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746254893
CDS Mutation c.1763G>A
AA Mutation p.Arg588His(p.R588H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9535918:9535918(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749079878
CDS Mutation c.1949G>A
AA Mutation p.Arg650Lys(p.R650K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9535699:9535699(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1730T>G
AA Mutation p.Ile577Ser(p.I577S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000019317
Start 9517201:9517201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.601A>G
AA Mutation p.Thr201Ala(p.T201A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000019317
Start 9530860:9530860(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1374G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000019317
Start 9513255:9513256(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.216dupA
AA Mutation p.Gly73ArgfsTer4(p.G73Rfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript