Primary Site >> Stomach Cancer

Gene >> ABL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318560
Start 130883992:130883992(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141983052
CDS Mutation c.1702G>A
AA Mutation p.Val568Met(p.V568M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318560
Start 130862961:130862961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.748G>A
AA Mutation p.Gly250Arg(p.G250R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318560
Start 130884093:130884093(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780716188
CDS Mutation c.1803C>A
AA Mutation p.Ser601Arg(p.S601R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318560
Start 130862779:130862779(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.566A>G
AA Mutation p.Glu189Gly(p.E189G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000318560
Start 130878484:130878484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1340A>C
AA Mutation p.Gln447Pro(p.Q447P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000318560
Start 130880529:130880529(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766145624
CDS Mutation c.1543G>A
AA Mutation p.Val515Ile(p.V515I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130884192:130884192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747192341
CDS Mutation c.1902C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130885035:130885035(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753006223
CDS Mutation c.2745G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130854898:130854898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141072111
CDS Mutation c.351G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130884468:130884468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2178C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130862909:130862909(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.696C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130862990:130862990(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754813636
CDS Mutation c.777C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000318560
Start 130885380:130885380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3090C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000318560
Start 130885226:130885226(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2940delC
AA Mutation p.Val981PhefsTer88(p.V981Ffs*88)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000318560
Start 130884637:130884637(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2352delC
AA Mutation p.Arg785GlyfsTer3(p.R785Gfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000318560
Start 130884019:130884019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1729C>T
AA Mutation p.Arg577Ter(p.R577*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000318560
Start 130872859:130872859(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.910delG
AA Mutation p.Val304SerfsTer15(p.X304_splice)
Mutation Classification Splice_Site
Feature Type Transcript