Primary Site >> Stomach Cancer

Gene >> MAP3K6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357582
Start 27362155:27362155(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750854600
CDS Mutation c.1351G>A
AA Mutation p.Ala451Thr(p.A451T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357582
Start 27362170:27362170(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1336G>A
AA Mutation p.Gly446Arg(p.G446R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357582
Start 27356417:27356417(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778526342
CDS Mutation c.3608G>A
AA Mutation p.Arg1203Gln(p.R1203Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357582
Start 27364882:27364882(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.371T>C
AA Mutation p.Leu124Pro(p.L124P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000357582
Start 27364856:27364856(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.397C>A
AA Mutation p.Leu133Ile(p.L133I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27360749:27360749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2010G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27360746:27360746(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780183265
CDS Mutation c.2013G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27362964:27362964(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1029G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27356724:27356724(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3390G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27357846:27357846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2946T>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27359969:27359969(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2208G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27361795:27361795(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1488G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27358736:27358736(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755931721
CDS Mutation c.2556C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000357582
Start 27360954:27360954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1887G>A
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000357582
Start 27358748:27358748(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs761519789
CDS Mutation c.2544delC
AA Mutation p.Phe849SerfsTer143(p.F849Sfs*143)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000357582
Start 27361205:27361205(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1784delC
AA Mutation p.Pro595ArgfsTer12(p.P595Rfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000357582
Start 27360931:27360932(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1909dupG
AA Mutation p.Glu637GlyfsTer6(p.E637Gfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 18
Mutation Consequence inframe_insertion
Transcription ID ENST00000357582
Start 27357052:27357053(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3318_3320dupACT
AA Mutation p.Leu1108dup(p.L1108dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript