Primary Site >> Liver Cancer

Gene >> WDFY3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84798028:84798028(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2903C>T
AA Mutation p.Pro968Leu(p.P968L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84803352:84803352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2545C>T
AA Mutation p.Pro849Ser(p.P849S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84718468:84718468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7708A>T
AA Mutation p.Met2570Leu(p.M2570L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84860455:84860455(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.137A>T
AA Mutation p.Glu46Val(p.E46V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84705450:84705450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8279C>T
AA Mutation p.Thr2760Ile(p.T2760I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84836945:84836945(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.560A>T
AA Mutation p.Gln187Leu(p.Q187L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84780242:84780242(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4231G>C
AA Mutation p.Ala1411Pro(p.A1411P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84757111:84757111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5239A>T
AA Mutation p.Asn1747Tyr(p.N1747Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000295888
Start 84789883:84789883(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3512C>T
AA Mutation p.Ser1171Leu(p.S1171L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84702426:84702426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8523A>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84741887:84741887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6108A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84741875:84741875(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6120A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000295888
Start 84786087:84786087(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3954A>G
Mutation Classification Silent
Feature Type Transcript