Primary Site >> Stomach Cancer

Gene >> ZNF33B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42593313:42593313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367988227
CDS Mutation c.1637C>T
AA Mutation p.Thr546Met(p.T546M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42593893:42593893(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756187933
CDS Mutation c.1057G>A
AA Mutation p.Gly353Arg(p.G353R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42593720:42593720(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1230G>C
AA Mutation p.Glu410Asp(p.E410D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42632372:42632372(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.77G>C
AA Mutation p.Trp26Ser(p.W26S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42594320:42594320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.630G>C
AA Mutation p.Glu210Asp(p.E210D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42592842:42592842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2108G>A
AA Mutation p.Ser703Asn(p.S703N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42594132:42594132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.818G>A
AA Mutation p.Ser273Asn(p.S273N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42594384:42594384(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.566A>G
AA Mutation p.Glu189Gly(p.E189G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42593415:42593415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1535T>C
AA Mutation p.Leu512Pro(p.L512P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359467
Start 42593013:42593013(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1937T>C
AA Mutation p.Phe646Ser(p.F646S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000359467
Start 42593960:42593960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.990A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000359467
Start 42594032:42594032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.918T>C
Mutation Classification Silent
Feature Type Transcript