Mutation

Primary Site >> Stomach Cancer

Gene >> HS6ST3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96091239:96091239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96090974:96090974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>A
AA Mutation	p.Gly38Arg(p.G38R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96832782:96832782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000A>C
AA Mutation	p.Asn334His(p.N334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96090987:96090987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96832963:96832963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377277765
CDS Mutation	c.1181G>A
AA Mutation	p.Arg394His(p.R394H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96832902:96832902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120T>C
AA Mutation	p.Ser374Pro(p.S374P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96091238:96091238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Cys(p.R126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96832833:96832833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051T>C
AA Mutation	p.Phe351Leu(p.F351L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376705
Start	96833082:96833082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200597659
CDS Mutation	c.1300C>T
AA Mutation	p.Arg434Trp(p.R434W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376705
Start	96091297:96091297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376705
Start	96091006:96091006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376705
Start	96090991:96090991(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.133delG
AA Mutation	p.Glu45ArgfsTer87(p.E45Rfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript