Mutation

Primary Site >> Stomach Cancer

Gene >> RASGRF1

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000419573
Start	79003803:79003803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2496G>C
AA Mutation	p.Gln832His(p.Q832H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046966:79046966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757215822
CDS Mutation	c.658C>T
AA Mutation	p.Arg220Trp(p.R220W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79006250:79006250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779403459
CDS Mutation	c.2050G>A
AA Mutation	p.Ala684Thr(p.A684T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046869:79046869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755A>C
AA Mutation	p.Glu252Ala(p.E252A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79058356:79058356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509A>C
AA Mutation	p.Glu170Ala(p.E170A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79027821:79027821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434Gln(p.R434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79049561:79049561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046813:79046813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Trp(p.R271W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78998121:78998121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Trp(p.R997W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046953:79046953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671C>T
AA Mutation	p.Thr224Ile(p.T224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79031466:79031466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196C>T
AA Mutation	p.Thr399Met(p.T399M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78999766:78999766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759233302
CDS Mutation	c.2771G>A
AA Mutation	p.Arg924Gln(p.R924Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79012508:79012508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846A>G
AA Mutation	p.Arg616Gly(p.R616G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046822:79046822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79004103:79004103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144984287
CDS Mutation	c.2196C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79004049:79004049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79064449:79064449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374689418
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79031495:79031495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78991753:78991753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141077574
CDS Mutation	c.3117C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79064485:79064485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79025392:79025392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113957070
CDS Mutation	c.1464C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79090469:79090469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419573
Start	79004115:79004115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2184delC
AA Mutation	p.Lys729SerfsTer31(p.K729Sfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419573
Start	78998816:78998816(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2804delC
AA Mutation	p.Pro935GlnfsTer11(p.P935Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript