Mutation

Primary Site >> Stomach Cancer

Gene >> ZMYM2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20002924:20002924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922G>A
AA Mutation	p.Ala308Thr(p.A308T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20051490:20051490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746386044
CDS Mutation	c.2350C>T
AA Mutation	p.Arg784Cys(p.R784C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20066999:20066999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3281T>C
AA Mutation	p.Val1094Ala(p.V1094A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20058662:20058662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2581A>G
AA Mutation	p.Thr861Ala(p.T861A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	19993781:19993781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709T>G
AA Mutation	p.Phe237Val(p.F237V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000382871
Start	19993917:19993917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845C>A
AA Mutation	p.Pro282His(p.P282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20085837:20085837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3957T>A
AA Mutation	p.Asn1319Lys(p.N1319K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20034380:20034380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759603248
CDS Mutation	c.2095G>A
AA Mutation	p.Val699Ile(p.V699I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382871
Start	20034348:20034348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063A>C
AA Mutation	p.Lys688Thr(p.K688T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382871
Start	20064503:20064503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199880478
CDS Mutation	c.3090C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382871
Start	20066995:20066995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3277C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382871
Start	20066943:20066943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3225C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382871
Start	20082954:20082954(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3749delA
AA Mutation	p.Asn1250IlefsTer3(p.N1250Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382871
Start	20061124:20061124(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2815delA
AA Mutation	p.Ser939AlafsTer15(p.S939Afs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382871
Start	20064537:20064537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753611080
CDS Mutation	c.3131delA
AA Mutation	p.Lys1044ArgfsTer33(p.K1044Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382871
Start	19993333:19993333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.266delA
AA Mutation	p.Asn89MetfsTer25(p.N89Mfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000382871
Start	19993493:19993493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Ter(p.R141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000382871
Start	20005192:20005192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252G>T
AA Mutation	p.Gly418Ter(p.G418*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript