Mutation

Primary Site >> Stomach Cancer

Gene >> SULF2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47666396:47666396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373071532
CDS Mutation	c.1669G>A
AA Mutation	p.Ala557Thr(p.A557T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47678710:47678710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159C>A
AA Mutation	p.Leu387Ile(p.L387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47702559:47702559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775009035
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Gln(p.R176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47678751:47678751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118C>T
AA Mutation	p.Ala373Val(p.A373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47690222:47690222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>T
AA Mutation	p.Arg214Met(p.R214M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47676528:47676528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346C>T
AA Mutation	p.Ala449Val(p.A449V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47736913:47736913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549518880
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Cys(p.R69C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47666485:47666485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580A>G
AA Mutation	p.Tyr527Cys(p.Y527C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359930
Start	47683142:47683142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.916G>A
AA Mutation	p.Glu306Lys(p.E306K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47663586:47663586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2094G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47702555:47702555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47663508:47663508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150627838
CDS Mutation	c.2172C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47672322:47672322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767497898
CDS Mutation	c.1452C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47666346:47666346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1719C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47678684:47678684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140200890
CDS Mutation	c.1185G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47736890:47736890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375623139
CDS Mutation	c.228G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359930
Start	47690263:47690263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200381009
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359930
Start	47661794:47661794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2473delC
AA Mutation	p.Arg825GlyfsTer29(p.R825Gfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359930
Start	47672211:47672211(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1563delA
AA Mutation	p.Lys521AsnfsTer31(p.K521Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359930
Start	47690187:47690187(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.676delC
AA Mutation	p.His226ThrfsTer43(p.H226Tfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359930
Start	47672210:47672211(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1563dupA
AA Mutation	p.Leu522ThrfsTer34(p.L522Tfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359930
Start	47661772:47661772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2494+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript