Primary Site >> Stomach Cancer

Gene >> ANLN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265748
Start 36449771:36449771(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140729544
CDS Mutation c.3185G>A
AA Mutation p.Arg1062Gln(p.R1062Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265748
Start 36407840:36407840(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs564754015
CDS Mutation c.980C>T
AA Mutation p.Thr327Met(p.T327M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265748
Start 36396299:36396299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.52A>C
AA Mutation p.Asn18His(p.N18H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265748
Start 36399348:36399348(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.442A>C
AA Mutation p.Lys148Gln(p.K148Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265748
Start 36426028:36426028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2762A>C
AA Mutation p.His921Pro(p.H921P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265748
Start 36399097:36399097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.191C>T
AA Mutation p.Pro64Leu(p.P64L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000265748
Start 36415769:36415769(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1407T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000265748
Start 36423854:36423854(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2514A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000265748
Start 36407946:36407946(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1086T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000265748
Start 36452540:36452540(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3315T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000265748
Start 36415785:36415785(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1428delA
AA Mutation p.Lys476AsnfsTer13(p.K476Nfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript