Primary Site >> Stomach Cancer

Gene >> FZR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3525969:3525969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.171G>C
AA Mutation p.Trp57Cys(p.W57C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3527785:3527785(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.625G>A
AA Mutation p.Val209Met(p.V209M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3534503:3534503(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543420977
CDS Mutation c.1430G>A
AA Mutation p.Arg477His(p.R477H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3532480:3532480(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1072G>A
AA Mutation p.Val358Met(p.V358M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3523012:3523012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.23G>A
AA Mutation p.Arg8His(p.R8H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3527010:3527010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.418G>A
AA Mutation p.Asp140Asn(p.D140N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000395095
Start 3523021:3523021(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772245619
CDS Mutation c.32G>A
AA Mutation p.Arg11His(p.R11H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000395095
Start 3533302:3533302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1251G>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000395095
Start 3532527:3532527(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1124delG
AA Mutation p.Gly375AlafsTer14(p.G375Afs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000395095
Start 3527036:3527036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.444C>G
AA Mutation p.Tyr148Ter(p.Y148*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript