Mutation

Primary Site >> Stomach Cancer

Gene >> ADGRE5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242786
Start	14396395:14396395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372889912
CDS Mutation	c.400G>A
AA Mutation	p.Val134Ile(p.V134I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242786
Start	14408098:14408098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2485A>G
AA Mutation	p.Arg829Gly(p.R829G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242786
Start	14406444:14406444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1935C>G
AA Mutation	p.Phe645Leu(p.F645L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242786
Start	14407141:14407141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780493480
CDS Mutation	c.2288G>A
AA Mutation	p.Arg763Gln(p.R763Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242786
Start	14397169:14397169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571G>A
AA Mutation	p.Gly191Ser(p.G191S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242786
Start	14391001:14391001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372021393
CDS Mutation	c.268G>A
AA Mutation	p.Asp90Asn(p.D90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242786
Start	14406724:14406724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242786
Start	14405852:14405852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242786
Start	14397213:14397213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242786
Start	14391063:14391063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140836731
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242786
Start	14407196:14407197(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2344_2347dupCTCT
AA Mutation	p.Tyr783SerfsTer105(p.Y783Sfs*105)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000242786
Start	14406387:14406389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1880_1882delTCT
AA Mutation	p.Phe627del(p.F627del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000242786
Start	14406912:14406914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2161_2163delAAG
AA Mutation	p.Lys721del(p.K721del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript