Mutation

Primary Site >> Stomach Cancer

Gene >> AXIN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	304405:304405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153C>G
AA Mutation	p.Pro385Ala(p.P385A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346908:346908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753659585
CDS Mutation	c.118G>A
AA Mutation	p.Ala40Thr(p.A40T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346464:346464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Glu188Lys(p.E188K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262320
Start	304441:304441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140421619
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Cys(p.R373C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	289512:289512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2390G>A
AA Mutation	p.Arg797His(p.R797H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346838:346838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759464398
CDS Mutation	c.188G>A
AA Mutation	p.Arg63His(p.R63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	346788:346788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238C>A
AA Mutation	p.Pro80Thr(p.P80T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	304351:304351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Trp(p.R403W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262320
Start	289492:289492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764818271
CDS Mutation	c.2410G>A
AA Mutation	p.Ala804Thr(p.A804T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	346381:346381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750806931
CDS Mutation	c.645G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	346309:346309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527251369
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	297940:297940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569298843
CDS Mutation	c.1566G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	289583:289583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368430061
CDS Mutation	c.2319C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262320
Start	314605:314605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	297983:297983(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs760961378
CDS Mutation	c.1523delG
AA Mutation	p.Gly508ValfsTer197(p.G508Vfs*197)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	346234:346234(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.792delC
AA Mutation	p.Gly265GlufsTer149(p.G265Efs*149)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	289452:289452(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2450delA
AA Mutation	p.Lys817ArgfsTer11(p.K817Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262320
Start	297093:297093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1918delG
AA Mutation	p.Glu640LysfsTer65(p.E640Kfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000262320
Start	297814:297814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1692G>A
AA Mutation	p.Trp564Ter(p.W564*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript