Primary Site >> Stomach Cancer

Gene >> ZNF354C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179079223:179079223(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746981450
CDS Mutation c.791G>T
AA Mutation p.Arg264Ile(p.R264I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179078904:179078904(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.472G>A
AA Mutation p.Gly158Arg(p.G158R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179079746:179079746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1314A>C
AA Mutation p.Lys438Asn(p.K438N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179078733:179078733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.301T>G
AA Mutation p.Phe101Val(p.F101V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179079621:179079621(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1189G>A
AA Mutation p.Val397Ile(p.V397I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179076472:179076472(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138654012
CDS Mutation c.55G>A
AA Mutation p.Val19Met(p.V19M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179078884:179078884(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.452A>T
AA Mutation p.Glu151Val(p.E151V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000315475
Start 179079073:179079073(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.641A>G
AA Mutation p.Lys214Arg(p.K214R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000315475
Start 179078937:179078937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.505T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000315475
Start 179079880:179079880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1448T>G
AA Mutation p.Leu483Ter(p.L483*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript