Primary Site >> Esophagus Cancer

Gene >> C3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6690714:6690714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3404A>G
AA Mutation p.Asn1135Ser(p.N1135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6697498:6697498(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2642G>A
AA Mutation p.Arg881His(p.R881H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6694461:6694461(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550043629
CDS Mutation c.3124C>T
AA Mutation p.Arg1042Trp(p.R1042W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6712600:6712600(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772505177
CDS Mutation c.1027C>T
AA Mutation p.Arg343Cys(p.R343C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6719269:6719269(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753544234
CDS Mutation c.209C>T
AA Mutation p.Ser70Phe(p.S70F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6694560:6694560(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3025G>T
AA Mutation p.Gly1009Cys(p.G1009C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000245907
Start 6697503:6697503(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2637G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000245907
Start 6692993:6692993(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3321G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000245907
Start 6697470:6697470(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2670delC
AA Mutation p.Lys891SerfsTer13(p.K891Sfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript