Primary Site >> Stomach Cancer

Gene >> HK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74873337:74873337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.557T>C
AA Mutation p.Val186Ala(p.V186A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74867768:74867768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.359G>A
AA Mutation p.Arg120Gln(p.R120Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74867659:74867659(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.250G>T
AA Mutation p.Asp84Tyr(p.D84Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74873938:74873938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.686T>C
AA Mutation p.Ile229Thr(p.I229T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74886526:74886526(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746400081
CDS Mutation c.2072G>A
AA Mutation p.Arg691His(p.R691H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74874280:74874280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.706G>A
AA Mutation p.Ala236Thr(p.A236T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74881837:74881837(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1697T>C
AA Mutation p.Val566Ala(p.V566A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74889342:74889342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2473G>A
AA Mutation p.Val825Met(p.V825M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74889456:74889456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2587A>G
AA Mutation p.Thr863Ala(p.T863A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74889316:74889316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2447G>A
AA Mutation p.Ser816Asn(p.S816N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74872316:74872316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.392C>T
AA Mutation p.Ala131Val(p.A131V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74874271:74874271(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.697G>T
AA Mutation p.Gly233Cys(p.G233C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000290573
Start 74885532:74885532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1878T>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000290573
Start 74834596:74834596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.16C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000290573
Start 74880290:74880290(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1291delG
AA Mutation p.Val431CysfsTer26(p.V431Cfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript