Mutation

Primary Site >> Stomach Cancer

Gene >> ADGRG2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19013818:19013818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>A
AA Mutation	p.Glu323Lys(p.E323K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379869
Start	18994897:18994897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2868T>A
AA Mutation	p.Asn956Lys(p.N956K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19013724:19013724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061C>T
AA Mutation	p.Ala354Val(p.A354V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19013874:19013874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911C>T
AA Mutation	p.Pro304Leu(p.P304L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19027253:19027253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436A>G
AA Mutation	p.Thr146Ala(p.T146A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19027228:19027228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>T
AA Mutation	p.Ser154Ile(p.S154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19010686:19010686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192G>A
AA Mutation	p.Ala398Thr(p.A398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19013866:19013866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919T>C
AA Mutation	p.Ser307Pro(p.S307P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379869
Start	19023432:19023432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532A>G
AA Mutation	p.Thr178Ala(p.T178A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379869
Start	19010632:19010632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379869
Start	19006014:19006014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186603149
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379869
Start	19028231:19028231(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.366delT
AA Mutation	p.Phe122LeufsTer21(p.F122Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379869
Start	18999088:18999088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2522delT
AA Mutation	p.Leu841TyrfsTer4(p.L841Yfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000379869
Start	19002844:19002844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2230+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript