Primary Site >> Stomach Cancer

Gene >> KDR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55113440:55113440(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.840G>C
AA Mutation p.Gln280His(p.Q280H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102424:55102424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2072C>A
AA Mutation p.Ser691Tyr(p.S691Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55090023:55090023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3125T>C
AA Mutation p.Val1042Ala(p.V1042A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102004:55102004(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375909858
CDS Mutation c.2159G>A
AA Mutation p.Arg720Gln(p.R720Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55125266:55125266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.28G>A
AA Mutation p.Ala10Thr(p.A10T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55098794:55098794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2276A>T
AA Mutation p.Glu759Val(p.E759V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55115288:55115288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.482T>G
AA Mutation p.Leu161Arg(p.L161R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55080011:55080011(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4001T>C
AA Mutation p.Val1334Ala(p.V1334A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55106747:55106747(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1476G>T
AA Mutation p.Gln492His(p.Q492H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55096337:55096337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2620G>A
AA Mutation p.Ala874Thr(p.A874T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55092639:55092639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3047T>A
AA Mutation p.Met1016Lys(p.M1016K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55114153:55114153(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55104857:55104857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1773G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55118614:55118614(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.348C>G
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55114189:55114189(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.735T>C
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55096314:55096314(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2643T>C
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55106746:55106746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1477G>T
AA Mutation p.Gly493Ter(p.G493*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55092622:55092622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3064C>T
AA Mutation p.Arg1022Ter(p.R1022*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000263923
Start 55081950:55081958(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3846_3848+6delTGGGTAAGA
Mutation Classification Splice_Site
Feature Type Transcript