Primary Site >> Stomach Cancer

Gene >> C1orf56

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368926
Start 151047900:151047900(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755921942
CDS Mutation c.53C>T
AA Mutation p.Pro18Leu(p.P18L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368926
Start 151048029:151048029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182G>T
AA Mutation p.Arg61Met(p.R61M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368926
Start 151047957:151047957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.110G>A
AA Mutation p.Ser37Asn(p.S37N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368926
Start 151048754:151048754(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.907G>A
AA Mutation p.Ala303Thr(p.A303T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368926
Start 151048684:151048684(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.837C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000368926
Start 151048707:151048707(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.864delC
AA Mutation p.Phe289SerfsTer48(p.F289Sfs*48)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000368926
Start 151048852:151048855(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1005+3_1005+6delAAGT
Mutation Classification Splice_Site
Feature Type Transcript