Primary Site >> Stomach Cancer

Gene >> DNMT3A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25240373:25240373(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750962348
CDS Mutation c.2251T>A
AA Mutation p.Phe751Ile(p.F751I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25241652:25241652(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1992G>T
AA Mutation p.Glu664Asp(p.E664D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25241618:25241618(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375399431
CDS Mutation c.2026C>T
AA Mutation p.Arg676Trp(p.R676W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25275005:25275005(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.575C>T
AA Mutation p.Ala192Val(p.A192V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25246282:25246282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1307A>G
AA Mutation p.Tyr436Cys(p.Y436C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264709
Start 25240439:25240439(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200018028
CDS Mutation c.2185C>T
AA Mutation p.Arg729Trp(p.R729W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264709
Start 25241655:25241655(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1989G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264709
Start 25282553:25282553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779949977
CDS Mutation c.336C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000264709
Start 25274965:25274965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.615G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000264709
Start 25246024:25246024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1470T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000264709
Start 25246222:25246222(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1367delA
AA Mutation p.Lys456SerfsTer195(p.K456Sfs*195)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000264709
Start 25300140:25300140(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.176delC
AA Mutation p.Pro59ArgfsTer13(p.P59Rfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript