Primary Site >> Stomach Cancer

Gene >> ECE1

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000374893
Start 21225438:21225438(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1852C>T
AA Mutation p.Arg618Trp(p.R618W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374893
Start 21256084:21256084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372050311
CDS Mutation c.883G>A
AA Mutation p.Gly295Arg(p.G295R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374893
Start 21258770:21258770(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.685G>A
AA Mutation p.Ala229Thr(p.A229T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374893
Start 21220095:21220095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754109847
CDS Mutation c.2173G>A
AA Mutation p.Glu725Lys(p.E725K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374893
Start 21279223:21279223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.248G>A
AA Mutation p.Cys83Tyr(p.C83Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000374893
Start 21256032:21256032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.935C>T
AA Mutation p.Thr312Met(p.T312M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000374893
Start 21272880:21272880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.312T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000374893
Start 21225367:21225367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1923G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000374893
Start 21227975:21227975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1737G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000374893
Start 21236846:21236846(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1390-2A>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 11
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000374893
Start 21227228:21227228(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1782-2A>G
Mutation Classification Splice_Site
Feature Type Transcript