Primary Site >> Esophagus Cancer

Gene >> ADAMTS16

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5209112:5209112(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1471C>A
AA Mutation p.Leu491Ile(p.L491I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5318138:5318138(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372733019
CDS Mutation c.3416C>T
AA Mutation p.Thr1139Met(p.T1139M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5242075:5242075(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755952454
CDS Mutation c.2546C>A
AA Mutation p.Pro849Gln(p.P849Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5232435:5232435(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1769C>T
AA Mutation p.Ser590Leu(p.S590L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5303341:5303341(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2863A>G
AA Mutation p.Thr955Ala(p.T955A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5235102:5235102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1939T>G
AA Mutation p.Phe647Val(p.F647V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000274181
Start 5182159:5182159(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.617A>G
AA Mutation p.Lys206Arg(p.K206R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000274181
Start 5239847:5239847(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2445T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000274181
Start 5140693:5140693(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.102G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000274181
Start 5242068:5242068(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2539A>C
Mutation Classification Silent
Feature Type Transcript