Primary Site >> Stomach Cancer

Gene >> HSPD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000345042
Start 197497281:197497281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.286A>G
AA Mutation p.Lys96Glu(p.K96E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000345042
Start 197495294:197495294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.510G>T
AA Mutation p.Gln170His(p.Q170H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000345042
Start 197487917:197487917(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1510G>A
AA Mutation p.Asp504Asn(p.D504N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000345042
Start 197489074:197489074(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1143A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000345042
Start 197487193:197487193(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1575G>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000345042
Start 197489140:197489140(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1077delA
AA Mutation p.Gly360GlufsTer19(p.G360Efs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence inframe_deletion
Transcription ID ENST00000345042
Start 197487056:197487067(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1701_1712delTATGGGAGGTGG
AA Mutation p.Met568_Gly571del(p.M568_G571del)
Mutation Classification In_Frame_Del
Feature Type Transcript
ID 8
Mutation Consequence inframe_deletion
Transcription ID ENST00000345042
Start 197487068:197487079(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1689_1700delAATGGGAGGTGG
AA Mutation p.Gly567_Gly570del(p.G567_G570del)
Mutation Classification In_Frame_Del
Feature Type Transcript