Primary Site >> Stomach Cancer

Gene >> PHEX

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22077590:22077590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.551A>G
AA Mutation p.Lys184Arg(p.K184R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22099033:22099033(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.961G>A
AA Mutation p.Val321Ile(p.V321I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22033070:22033070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.65C>T
AA Mutation p.Ala22Val(p.A22V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22111493:22111493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1106G>T
AA Mutation p.Arg369Ile(p.R369I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22114509:22114509(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754314481
CDS Mutation c.1225T>C
AA Mutation p.Phe409Leu(p.F409L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22212941:22212941(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1683G>T
AA Mutation p.Trp561Cys(p.W561C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22077622:22077622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.583C>T
AA Mutation p.Arg195Cys(p.R195C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000379374
Start 22178341:22178341(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1551T>G
AA Mutation p.Asp517Glu(p.D517E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000379374
Start 22099104:22099104(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1032G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000379374
Start 22077564:22077564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.525C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000379374
Start 22094026:22094026(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.779delT
AA Mutation p.Leu260Ter(p.L260*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000379374
Start 22245402:22245402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2140C>T
AA Mutation p.Gln714Ter(p.Q714*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000379374
Start 22096976:22096976(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.871C>T
AA Mutation p.Arg291Ter(p.R291*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000379374
Start 22226485:22226485(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1942G>T
AA Mutation p.Gly648Ter(p.G648*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript