Primary Site >> Stomach Cancer

Gene >> ZNF471

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56525289:56525289(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1222T>C
AA Mutation p.Cys408Arg(p.C408R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56516396:56516396(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773139042
CDS Mutation c.155C>T
AA Mutation p.Ser52Leu(p.S52L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56524414:56524414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.347T>G
AA Mutation p.Leu116Arg(p.L116R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56525115:56525115(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766567776
CDS Mutation c.1048G>A
AA Mutation p.Glu350Lys(p.E350K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56525155:56525155(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142290015
CDS Mutation c.1088G>A
AA Mutation p.Arg363His(p.R363H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56524414:56524414(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.347T>A
AA Mutation p.Leu116His(p.L116H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56524912:56524912(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.845G>C
AA Mutation p.Arg282Thr(p.R282T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000308031
Start 56524899:56524899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.832A>T
AA Mutation p.Ile278Phe(p.I278F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56525945:56525945(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1878T>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56516313:56516313(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.72C>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56525609:56525609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1542T>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56525714:56525714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1647G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56525030:56525030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.963A>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56525357:56525357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1290T>C
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000308031
Start 56525177:56525177(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1110T>C
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000308031
Start 56525079:56525079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1012A>T
AA Mutation p.Arg338Ter(p.R338*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript