Primary Site >> Esophagus Cancer

Gene >> FAT2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521309:151521309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751829289
CDS Mutation c.11284C>T
AA Mutation p.Arg3762Trp(p.R3762W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151567094:151567094(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1838A>G
AA Mutation p.Asn613Ser(p.N613S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151521468:151521468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11125G>A
AA Mutation p.Glu3709Lys(p.E3709K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151549501:151549501(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756688058
CDS Mutation c.4583G>A
AA Mutation p.Arg1528Gln(p.R1528Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543536:151543536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7591A>G
AA Mutation p.Ile2531Val(p.I2531V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151507259:151507259(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144848990
CDS Mutation c.12412C>T
AA Mutation p.Arg4138Trp(p.R4138W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151544469:151544469(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6658T>G
AA Mutation p.Phe2220Val(p.F2220V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151542666:151542666(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8461G>T
AA Mutation p.Ala2821Ser(p.A2821S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543451:151543451(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7676C>T
AA Mutation p.Ala2559Val(p.A2559V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261800
Start 151543452:151543452(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7675G>T
AA Mutation p.Ala2559Ser(p.A2559S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151544110:151544110(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7017T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000261800
Start 151531636:151531636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9762C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000261800
Start 151568736:151568736(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.196C>T
AA Mutation p.Gln66Ter(p.Q66*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript