Mutation

Primary Site >> Stomach Cancer

Gene >> ADGRL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14163085:14163085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731G>A
AA Mutation	p.Ser244Asn(p.S244N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14159119:14159119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2135C>T
AA Mutation	p.Ala712Val(p.A712V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14160228:14160228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149895143
CDS Mutation	c.1699G>A
AA Mutation	p.Ala567Thr(p.A567T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14158412:14158412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305G>A
AA Mutation	p.Ala769Thr(p.A769T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162914:14162914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201495192
CDS Mutation	c.902G>A
AA Mutation	p.Arg301His(p.R301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14162645:14162645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138963845
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Cys(p.R391C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14151220:14151220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4078G>C
AA Mutation	p.Glu1360Gln(p.E1360Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14155511:14155511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3157G>A
AA Mutation	p.Ala1053Thr(p.A1053T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14177612:14177612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203A>T
AA Mutation	p.Asp68Val(p.D68V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14158429:14158429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2288T>G
AA Mutation	p.Val763Gly(p.V763G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14161405:14161405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1432C>T
AA Mutation	p.Leu478Phe(p.L478F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14170774:14170774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302A>G
AA Mutation	p.Gln101Arg(p.Q101R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14160643:14160643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1579C>A
AA Mutation	p.Pro527Thr(p.P527T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14150902:14150902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779694675
CDS Mutation	c.4396G>A
AA Mutation	p.Gly1466Arg(p.G1466R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14163034:14163034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368468552
CDS Mutation	c.782G>A
AA Mutation	p.Arg261His(p.R261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14158498:14158498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2219C>T
AA Mutation	p.Thr740Met(p.T740M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14170757:14170757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375084597
CDS Mutation	c.319G>A
AA Mutation	p.Gly107Ser(p.G107S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14160601:14160601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>A
AA Mutation	p.Ala541Thr(p.A541T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000340736
Start	14155510:14155510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3158C>T
AA Mutation	p.Ala1053Val(p.A1053V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14158497:14158497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2220G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14163132:14163132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14177677:14177677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562415321
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14157128:14157128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374454857
CDS Mutation	c.2778C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14162619:14162619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754091921
CDS Mutation	c.1197C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14163084:14163084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569059104
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14161577:14161577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14177626:14177626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148289324
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340736
Start	14157443:14157443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768775667
CDS Mutation	c.2568C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340736
Start	14152848:14152848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3374delG
AA Mutation	p.Gly1125AlafsTer33(p.G1125Afs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000340736
Start	14159586:14159586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript