Primary Site >> Stomach Cancer

Gene >> MAP4K4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101869719:101869719(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs545368433
CDS Mutation c.2318C>T
AA Mutation p.Thr773Met(p.T773M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101839967:101839967(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779064004
CDS Mutation c.922C>T
AA Mutation p.Arg308Cys(p.R308C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101859072:101859072(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1472C>T
AA Mutation p.Ala491Val(p.A491V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101874161:101874161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2715T>A
AA Mutation p.Asn905Lys(p.N905K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101882568:101882568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2968C>T
AA Mutation p.Arg990Cys(p.R990C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101887797:101887797(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3356C>A
AA Mutation p.Pro1119His(p.P1119H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101869706:101869706(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2305G>A
AA Mutation p.Glu769Lys(p.E769K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000347699
Start 101698504:101698504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.89T>C
AA Mutation p.Val30Ala(p.V30A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000347699
Start 101859786:101859786(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763922718
CDS Mutation c.1626G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000347699
Start 101859780:101859780(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762602382
CDS Mutation c.1620A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000347699
Start 101859753:101859753(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs186857052
CDS Mutation c.1593G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000347699
Start 101869669:101869669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2268G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000347699
Start 101835970:101835971(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.770_771delAA
AA Mutation p.Lys257MetfsTer7(p.K257Mfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000347699
Start 101844282:101844300(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1204_1222delCAGAAAGAACAGAGGCGAC
AA Mutation p.Gln402GlyfsTer2(p.Q402Gfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000347699
Start 101831801:101831813(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.593_605delAGGTCATCGCCTG
AA Mutation p.Glu198ValfsTer38(p.E198Vfs*38)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000347699
Start 101844297:101844297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1219C>T
AA Mutation p.Arg407Ter(p.R407*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000347699
Start 101835969:101835970(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.771dupA
AA Mutation p.Trp258MetfsTer7(p.W258Mfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript