Primary Site >> Liver Cancer

Gene >> C3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6693482:6693482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3160A>G
AA Mutation p.Thr1054Ala(p.T1054A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6690679:6690679(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3439G>T
AA Mutation p.Val1147Phe(p.V1147F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6713469:6713469(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.814A>G
AA Mutation p.Ile272Val(p.I272V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6714371:6714371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.580G>A
AA Mutation p.Asp194Asn(p.D194N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6710799:6710799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1526A>G
AA Mutation p.Glu509Gly(p.E509G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6693470:6693470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3172G>T
AA Mutation p.Ala1058Ser(p.A1058S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6682225:6682225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4177C>G
AA Mutation p.Arg1393Gly(p.R1393G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000245907
Start 6707889:6707889(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1886C>T
AA Mutation p.Pro629Leu(p.P629L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000245907
Start 6697539:6697539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2601C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000245907
Start 6713196:6713196(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000245907
Start 6677897:6677897(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4977T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000245907
Start 6678282:6678282(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4720delG
AA Mutation p.Asp1574MetfsTer21(p.D1574Mfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000245907
Start 6684821:6684822(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3982_3983insGGCTCAAACCTGGGCCTTTAGGGCGGCCC
AA Mutation p.Glu1328GlyfsTer28(p.E1328Gfs*28)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript