Primary Site >> Stomach Cancer

Gene >> ZNF610

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321287
Start 52354305:52354305(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.245C>T
AA Mutation p.Pro82Leu(p.P82L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321287
Start 52353712:52353712(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769038010
CDS Mutation c.94G>A
AA Mutation p.Glu32Lys(p.E32K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321287
Start 52366280:52366280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753731698
CDS Mutation c.902C>T
AA Mutation p.Ser301Leu(p.S301L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321287
Start 52366408:52366408(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1030T>C
AA Mutation p.Tyr344His(p.Y344H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321287
Start 52354339:52354339(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.279A>C
AA Mutation p.Lys93Asn(p.K93N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000321287
Start 52366671:52366671(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1293T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000321287
Start 52366017:52366017(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.639T>C
Mutation Classification Silent
Feature Type Transcript