Primary Site >> Stomach Cancer

Gene >> NFATC3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000346183
Start 68122656:68122656(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.773G>A
AA Mutation p.Arg258Lys(p.R258K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000346183
Start 68123039:68123039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1156G>T
AA Mutation p.Asp386Tyr(p.D386Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000346183
Start 68122464:68122464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.581C>T
AA Mutation p.Ser194Leu(p.S194L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000346183
Start 68191071:68191071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2402C>T
AA Mutation p.Ser801Phe(p.S801F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000346183
Start 68191300:68191300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2631T>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000346183
Start 68126595:68126595(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1386A>G
Mutation Classification Silent
Feature Type Transcript