Primary Site >> Stomach Cancer

Gene >> CHD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98873601:98873601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3563A>G
AA Mutation p.Glu1188Gly(p.E1188G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98869777:98869777(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4084A>C
AA Mutation p.Lys1362Gln(p.K1362Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98900973:98900973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.697C>T
AA Mutation p.Arg233Cys(p.R233C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98888210:98888210(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758876162
CDS Mutation c.2374C>A
AA Mutation p.Leu792Ile(p.L792I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98858210:98858210(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4757G>A
AA Mutation p.Arg1586His(p.R1586H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98873598:98873598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3566G>A
AA Mutation p.Arg1189Gln(p.R1189Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000284049
Start 98905093:98905093(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778115031
CDS Mutation c.59C>T
AA Mutation p.Ser20Leu(p.S20L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000284049
Start 98858227:98858227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4740T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000284049
Start 98899530:98899530(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1035A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000284049
Start 98885590:98885590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2556T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000284049
Start 98872186:98872186(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3726C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000284049
Start 98901041:98901041(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.629delA
AA Mutation p.Lys210ArgfsTer39(p.K210Rfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000284049
Start 98870705:98870705(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3960delA
AA Mutation p.Glu1321LysfsTer22(p.E1321Kfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000284049
Start 98900815:98900815(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.855delA
AA Mutation p.Gly286GlufsTer34(p.G286Efs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000284049
Start 98899484:98899484(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1081delA
AA Mutation p.Arg361AspfsTer3(p.R361Dfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript