Mutation

Primary Site >> Stomach Cancer

Gene >> SRGAP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64108956:64108956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750241777
CDS Mutation	c.1838C>T
AA Mutation	p.Ala613Val(p.A613V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64127982:64127982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375183261
CDS Mutation	c.2662A>G
AA Mutation	p.Ser888Gly(p.S888G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64091326:64091326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149964620
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64097297:64097297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779089900
CDS Mutation	c.1735G>A
AA Mutation	p.Val579Ile(p.V579I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64111980:64111980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2138A>G
AA Mutation	p.Asp713Gly(p.D713G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64063089:64063089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773806400
CDS Mutation	c.974C>T
AA Mutation	p.Ala325Val(p.A325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64065134:64065134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040C>T
AA Mutation	p.Ala347Val(p.A347V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	63984106:63984106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Ala76Val(p.A76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355086
Start	64111928:64111928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2086G>T
AA Mutation	p.Asp696Tyr(p.D696Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64065201:64065201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64063090:64063090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745401734
CDS Mutation	c.975G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64126101:64126101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2349C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64127879:64127879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2559G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	64094940:64094940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355086
Start	63984026:63984026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	64127883:64127883(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2567delC
AA Mutation	p.Pro856LeufsTer3(p.P856Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355086
Start	63984041:63984041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.168delA
AA Mutation	p.Ala57LeufsTer11(p.A57Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript