Mutation

Primary Site >> Stomach Cancer

Gene >> AMBRA1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46397877:46397877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3470A>G
AA Mutation	p.Glu1157Gly(p.E1157G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46397766:46397766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762502501
CDS Mutation	c.3581C>T
AA Mutation	p.Thr1194Met(p.T1194M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46542768:46542768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249T>G
AA Mutation	p.Ser417Ala(p.S417A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46443535:46443535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2585T>C
AA Mutation	p.Leu862Pro(p.L862P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46434942:46434942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2728A>C
AA Mutation	p.Ser910Arg(p.S910R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46542707:46542707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373429644
CDS Mutation	c.1310C>T
AA Mutation	p.Pro437Leu(p.P437L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46547264:46547264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227A>C
AA Mutation	p.Asn76Thr(p.N76T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46408656:46408656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3260C>T
AA Mutation	p.Ala1087Val(p.A1087V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46542903:46542903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114A>G
AA Mutation	p.Ser372Gly(p.S372G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46397812:46397812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3535G>A
AA Mutation	p.Gly1179Ser(p.G1179S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46508294:46508294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2236A>G
AA Mutation	p.Met746Val(p.M746V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46443530:46443530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2590T>C
AA Mutation	p.Trp864Arg(p.W864R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46542214:46542214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1803G>T
AA Mutation	p.Gln601His(p.Q601H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46542779:46542779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238G>T
AA Mutation	p.Gly413Val(p.G413V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000458649
Start	46543346:46543346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760124943
CDS Mutation	c.671G>A
AA Mutation	p.Arg224His(p.R224H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46397870:46397870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3477C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46433546:46433546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2904C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46408619:46408619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3297G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46408604:46408604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3312C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46545705:46545705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46542202:46542202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1815C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458649
Start	46548306:46548306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458649
Start	46542707:46542707(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1310delC
AA Mutation	p.Pro437ArgfsTer9(p.P437Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458649
Start	46542075:46542075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1942delG
AA Mutation	p.Val648TrpfsTer84(p.V648Wfs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000458649
Start	46433563:46433563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2887C>T
AA Mutation	p.Arg963Ter(p.R963*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000458649
Start	46417920:46417920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3109C>T
AA Mutation	p.Arg1037Ter(p.R1037*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000458649
Start	46397677:46397677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3670C>T
AA Mutation	p.Arg1224Ter(p.R1224*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458649
Start	46547212:46547213(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.278dupG
AA Mutation	p.His94ThrfsTer28(p.H94Tfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458649
Start	46397487:46397488(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3859dupG
AA Mutation	p.Asp1287GlyfsTer6(p.D1287Gfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000458649
Start	46547112:46547112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript