Mutation

Primary Site >> Stomach Cancer

Gene >> AXIN2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65536477:65536477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1984C>A
AA Mutation	p.Leu662Met(p.L662M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65537465:65537465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1571T>A
AA Mutation	p.Val524Asp(p.V524D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65557950:65557950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671A>G
AA Mutation	p.Tyr224Cys(p.Y224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65536962:65536962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1814C>T
AA Mutation	p.Ala605Val(p.A605V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65549532:65549532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747647668
CDS Mutation	c.944C>T
AA Mutation	p.Thr315Met(p.T315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65541544:65541544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970C>T
AA Mutation	p.Pro324Ser(p.P324S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65536486:65536486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142670753
CDS Mutation	c.1975C>T
AA Mutation	p.Arg659Trp(p.R659W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000307078
Start	65557807:65557807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814A>T
AA Mutation	p.Arg272Trp(p.R272W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65530076:65530076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2432A>G
AA Mutation	p.Glu811Gly(p.E811G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65536383:65536383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755519590
CDS Mutation	c.2078C>T
AA Mutation	p.Thr693Met(p.T693M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307078
Start	65558131:65558131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490C>G
AA Mutation	p.Gln164Glu(p.Q164E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65558030:65558030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65557892:65557892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65529982:65529982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2526C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307078
Start	65537377:65537377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536467:65536467(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs267606674
CDS Mutation	c.1994delG
AA Mutation	p.Gly665AlafsTer24(p.G665Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536450:65536450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2011delC
AA Mutation	p.Arg671AlafsTer18(p.R671Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65558010:65558010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.611delG
AA Mutation	p.Gly204GlufsTer7(p.G204Efs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536981:65536981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1795delG
AA Mutation	p.Ala599ProfsTer90(p.A599Pfs*90)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307078
Start	65536437:65536438(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2023dupC
AA Mutation	p.Arg675ProfsTer32(p.R675Pfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript