Primary Site >> Stomach Cancer

Gene >> KLF4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107488123:107488123(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.271C>A
AA Mutation p.Leu91Ile(p.L91I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107488192:107488192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781269132
CDS Mutation c.202G>A
AA Mutation p.Ala68Thr(p.A68T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107487039:107487039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1253G>A
AA Mutation p.Arg418Gln(p.R418Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107485788:107485788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1403C>T
AA Mutation p.Ser468Leu(p.S468L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107487112:107487112(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747114701
CDS Mutation c.1180G>A
AA Mutation p.Ala394Thr(p.A394T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107487877:107487877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.517T>C
AA Mutation p.Tyr173His(p.Y173H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000374672
Start 107487958:107487958(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.436T>G
AA Mutation p.Ser146Ala(p.S146A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000374672
Start 107487497:107487497(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.897G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence inframe_insertion
Transcription ID ENST00000374672
Start 107485830:107485831(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1358_1360dupACC
AA Mutation p.His453dup(p.H453dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript