Mutation

Primary Site >> Stomach Cancer

Gene >> TNIP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151039186:151039186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765402343
CDS Mutation	c.1174C>T
AA Mutation	p.Arg392Cys(p.R392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151042580:151042580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375343575
CDS Mutation	c.1094G>A
AA Mutation	p.Arg365His(p.R365H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315050
Start	151030732:151030732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1892A>G
AA Mutation	p.Asp631Gly(p.D631G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315050
Start	151065078:151065078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765807266
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315050
Start	151056937:151056937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315050
Start	151056931:151056931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761715922
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315050
Start	151056820:151056820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748371382
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000315050
Start	151032347:151032347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Ter(p.R606*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000315050
Start	151042665:151042665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>T
AA Mutation	p.Glu337Ter(p.E337*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000315050
Start	151035065:151035078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1522-11_1524delTCTTCTCTCAGCTA
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	11
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000315050
Start	151035057:151035131(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1522-64_1532delGGATCCAGGCCTGGCCAGAAACCACCTGTGCCGACAGTCTTTTCTCCCTCCCTTCTTCTCTCAGCTAAAAGCATT
Mutation Classification	Splice_Site
Feature Type	Transcript