Mutation

Primary Site >> Stomach Cancer

Gene >> STAT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	191008975:191008975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>T
AA Mutation	p.Lys87Asn(p.K87N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	190983725:190983725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371982540
CDS Mutation	c.1363G>A
AA Mutation	p.Val455Ile(p.V455I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	190985626:190985626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256C>T
AA Mutation	p.Thr419Met(p.T419M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	190998299:190998299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>T
AA Mutation	p.Thr184Ile(p.T184I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	190978904:190978904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1825G>A
AA Mutation	p.Glu609Lys(p.E609K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	190986921:190986921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587777630
CDS Mutation	c.1154C>T
AA Mutation	p.Thr385Met(p.T385M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	190999667:190999667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>G
AA Mutation	p.Gln167Arg(p.Q167R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361099
Start	191009988:191009988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761876441
CDS Mutation	c.16G>A
AA Mutation	p.Glu6Lys(p.E6K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361099
Start	190976958:190976958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1941C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361099
Start	190995183:190995183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361099
Start	190983659:190983659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361099
Start	190995115:190995115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.890delA
AA Mutation	p.Asn297ThrfsTer39(p.N297Tfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361099
Start	190986852:190986852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript