Mutation

Primary Site >> Stomach Cancer

Gene >> SOX6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	15972828:15972828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2468A>C
AA Mutation	p.Glu823Ala(p.E823A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	16186808:16186808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683A>G
AA Mutation	p.Asp228Gly(p.D228G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	15972984:15972984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2312C>A
AA Mutation	p.Pro771His(p.P771H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	16046626:16046626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1511G>A
AA Mutation	p.Arg504Gln(p.R504Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	16055891:16055891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112C>T
AA Mutation	p.Ala371Val(p.A371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	15986395:15986395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992C>G
AA Mutation	p.Asn664Lys(p.N664K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	16318565:16318565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774770291
CDS Mutation	c.326G>A
AA Mutation	p.Arg109His(p.R109H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000528429
Start	15986300:15986300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2087G>A
AA Mutation	p.Arg696His(p.R696H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000528429
Start	16186798:16186798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000528429
Start	15973031:15973031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763382219
CDS Mutation	c.2265G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000528429
Start	16049867:16049867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000528429
Start	15973055:15973055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000528429
Start	16111823:16111823(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.878delC
AA Mutation	p.Pro293LeufsTer3(p.P293Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000528429
Start	16049832:16049833(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1357dupA
AA Mutation	p.Thr453AsnfsTer14(p.T453Nfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000528429
Start	15989064:15989065(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1898dupA
AA Mutation	p.Asp634GlyfsTer2(p.D634Gfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000528429
Start	16097607:16097607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript