Mutation

Primary Site >> Stomach Cancer

Gene >> STARD3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336308
Start	39660995:39660995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049T>C
AA Mutation	p.Val350Ala(p.V350A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336308
Start	39653598:39653598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>T
AA Mutation	p.Gly23Cys(p.G23C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336308
Start	39658459:39658459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484G>A
AA Mutation	p.Ala162Thr(p.A162T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336308
Start	39653683:39653683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751173622
CDS Mutation	c.152G>A
AA Mutation	p.Arg51His(p.R51H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336308
Start	39658755:39658755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581G>T
AA Mutation	p.Gly194Val(p.G194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336308
Start	39653659:39653659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149648909
CDS Mutation	c.128G>A
AA Mutation	p.Arg43Gln(p.R43Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336308
Start	39659505:39659505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336308
Start	39660448:39660448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336308
Start	39658500:39658500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525C>A
Mutation Classification	Silent
Feature Type	Transcript