Mutation

Primary Site >> Stomach Cancer

Gene >> ADAR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154590366:154590366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763229776
CDS Mutation	c.2314G>A
AA Mutation	p.Val772Ile(p.V772I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154589892:154589892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2533G>A
AA Mutation	p.Ala845Thr(p.A845T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154585039:154585039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3448C>T
AA Mutation	p.Arg1150Trp(p.R1150W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154597181:154597181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2021A>G
AA Mutation	p.Glu674Gly(p.E674G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154584954:154584954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3533T>C
AA Mutation	p.Leu1178Pro(p.L1178P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154588185:154588185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763536266
CDS Mutation	c.2959C>T
AA Mutation	p.Arg987Cys(p.R987C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154588578:154588578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2858A>G
AA Mutation	p.Lys953Arg(p.K953R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602301:154602301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770167108
CDS Mutation	c.341G>A
AA Mutation	p.Arg114His(p.R114H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154597916:154597916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570647049
CDS Mutation	c.1846G>A
AA Mutation	p.Val616Ile(p.V616I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602517:154602517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125A>G
AA Mutation	p.Lys42Arg(p.K42R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602488:154602488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.154C>T
AA Mutation	p.Pro52Ser(p.P52S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154596956:154596956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2119T>A
AA Mutation	p.Ser707Thr(p.S707T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368474
Start	154602215:154602215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427A>T
AA Mutation	p.Ile143Phe(p.I143F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154584911:154584911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768173047
CDS Mutation	c.3576C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154602426:154602426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368474
Start	154602249:154602249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368474
Start	154597917:154597917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1845delC
AA Mutation	p.Val616SerfsTer45(p.V616Sfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368474
Start	154584884:154584884(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3603delA
AA Mutation	p.Gly1202AlafsTer2(p.G1202Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368474
Start	154598544:154598544(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1643delC
AA Mutation	p.Pro548GlnfsTer16(p.P548Qfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript