Mutation

Primary Site >> Stomach Cancer

Gene >> SART3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108549123:108549123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108525564:108525564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416T>C
AA Mutation	p.Ser806Pro(p.S806P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108538992:108538992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375395577
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335His(p.R335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108530216:108530216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1841A>G
AA Mutation	p.Lys614Arg(p.K614R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108530228:108530228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202055950
CDS Mutation	c.1829C>T
AA Mutation	p.Ala610Val(p.A610V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108545243:108545243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776249648
CDS Mutation	c.625G>A
AA Mutation	p.Val209Met(p.V209M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108532308:108532308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1583G>A
AA Mutation	p.Arg528Gln(p.R528Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108530264:108530264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793C>T
AA Mutation	p.Ala598Val(p.A598V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108535437:108535437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478G>A
AA Mutation	p.Arg493Gln(p.R493Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108526298:108526298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2171C>G
AA Mutation	p.Pro724Arg(p.P724R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000228284
Start	108547926:108547926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562057224
CDS Mutation	c.505G>A
AA Mutation	p.Val169Met(p.V169M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228284
Start	108560870:108560870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751740249
CDS Mutation	c.285G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228284
Start	108526309:108526309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751321190
CDS Mutation	c.2160G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228284
Start	108524468:108524468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2562G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228284
Start	108526327:108526327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2142C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228284
Start	108523616:108523616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572381313
CDS Mutation	c.2733G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228284
Start	108532319:108532319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000228284
Start	108538200:108538200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Ter(p.R356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000228284
Start	108530283:108530283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774C>T
AA Mutation	p.Gln592Ter(p.Q592*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000228284
Start	108523477:108523477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2872A>T
AA Mutation	p.Lys958Ter(p.K958*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript