Primary Site >> Stomach Cancer

Gene >> AHCYL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369799
Start 110009080:110009080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.167C>T
AA Mutation p.Thr56Ile(p.T56I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369799
Start 110018409:110018409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768042207
CDS Mutation c.1160G>A
AA Mutation p.Arg387His(p.R387H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369799
Start 110012957:110012957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.538T>C
AA Mutation p.Tyr180His(p.Y180H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369799
Start 110014804:110014804(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.622T>G
AA Mutation p.Phe208Val(p.F208V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369799
Start 110018447:110018447(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1198T>C
AA Mutation p.Ser400Pro(p.S400P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369799
Start 109985086:109985086(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.34G>T
AA Mutation p.Val12Phe(p.V12F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000369799
Start 110020792:110020792(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755703351
CDS Mutation c.1527T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000369799
Start 110018578:110018578(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750594180
CDS Mutation c.1245G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000369799
Start 110016398:110016398(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.837T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000369799
Start 110019090:110019091(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1358_1359insCACCTGCCCTCTGACCTGCCCCT
AA Mutation p.Val454ThrfsTer21(p.V454Tfs*21)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000369799
Start 110020768:110020769(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1504_1508dupGCCCA
AA Mutation p.His503GlnfsTer7(p.H503Qfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 12
Mutation Consequence inframe_deletion;splice_region_variant
Transcription ID ENST00000369799
Start 110019090:110019119(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1357_1386delTTTGTTCTGTCCATCACAGCCACAACACAG
AA Mutation p.Phe453_Gln462del(p.F453_Q462del)
Mutation Classification In_Frame_Del
Feature Type Transcript
ID 13
Mutation Consequence inframe_insertion
Transcription ID ENST00000369799
Start 110019089:110019090(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1356_1357insACA
AA Mutation p.Thr452dup(p.T452dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript