Mutation

Primary Site >> Stomach Cancer

Gene >> APP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	26051075:26051075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587T>C
AA Mutation	p.Val196Ala(p.V196A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	26022026:26022026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Glu227Lys(p.E227K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	25975093:25975093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1435G>A
AA Mutation	p.Ala479Thr(p.A479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	26021939:26021939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.766G>A
AA Mutation	p.Glu256Lys(p.E256K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	25911870:25911870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780A>G
AA Mutation	p.Met594Val(p.M594V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	26053325:26053325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379C>A
AA Mutation	p.Leu127Ile(p.L127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	26112110:26112110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94C>G
AA Mutation	p.Pro32Ala(p.P32A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	25955746:25955746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468G>A
AA Mutation	p.Val490Met(p.V490M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346798
Start	26000152:26000152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202074408
CDS Mutation	c.896C>T
AA Mutation	p.Pro299Leu(p.P299L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	26053314:26053314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	26021979:26021979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200270161
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	25955678:25955678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	26000148:26000148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	26053272:26053272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199520480
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	25975121:25975121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1407C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	26053275:26053275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	26051140:26051140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199905579
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346798
Start	25891806:25891806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2127T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000346798
Start	25975222:25975222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306C>T
AA Mutation	p.Gln436Ter(p.Q436*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346798
Start	26051029:26051030(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.632dupG
AA Mutation	p.Gly212ArgfsTer11(p.G212Rfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript