Primary Site >> Esophagus Cancer

Gene >> PCDH10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152664:133152664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2524C>A
AA Mutation p.Pro842Thr(p.P842T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151030:133151030(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.890C>T
AA Mutation p.Ala297Val(p.A297V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150291:133150291(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367823724
CDS Mutation c.151C>T
AA Mutation p.Arg51Cys(p.R51C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150320:133150320(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.180G>C
AA Mutation p.Arg60Ser(p.R60S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150934:133150934(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.794C>A
AA Mutation p.Pro265Gln(p.P265Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151780:133151780(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1640A>T
AA Mutation p.Asp547Val(p.D547V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133150198:133150198(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.58C>A
AA Mutation p.Leu20Ile(p.L20I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151867:133151867(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1727C>T
AA Mutation p.Ala576Val(p.A576V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152397:133152397(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2257G>A
AA Mutation p.Ala753Thr(p.A753T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150188:133150188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.48C>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151082:133151082(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.942C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133152627:133152627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2487C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133150617:133150617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.477C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133151604:133151604(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1464C>T
Mutation Classification Silent
Feature Type Transcript