Mutation

Primary Site >> Stomach Cancer

Gene >> MAG

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35295793:35295793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Ser76Leu(p.S76L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35300192:35300192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758A>T
AA Mutation	p.Glu253Val(p.E253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35300369:35300369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>A
AA Mutation	p.Gly312Asp(p.G312D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35310039:35310039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397G>A
AA Mutation	p.Ser466Asn(p.S466N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35295718:35295718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200718920
CDS Mutation	c.152G>A
AA Mutation	p.Arg51Gln(p.R51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35300290:35300290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Glu286Lys(p.E286K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35295678:35295678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757733728
CDS Mutation	c.112G>A
AA Mutation	p.Val38Ile(p.V38I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35311982:35311982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201165241
CDS Mutation	c.1681G>A
AA Mutation	p.Asp561Asn(p.D561N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35295663:35295663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97T>C
AA Mutation	p.Phe33Leu(p.F33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35310612:35310612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585A>G
AA Mutation	p.Ile529Val(p.I529V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35302494:35302494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017G>C
AA Mutation	p.Glu339Asp(p.E339D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35295927:35295927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>A
AA Mutation	p.Leu121Met(p.L121M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35295909:35295909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343T>C
AA Mutation	p.Tyr115His(p.Y115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35310026:35310026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384T>C
AA Mutation	p.Tyr462His(p.Y462H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35310023:35310023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381G>A
AA Mutation	p.Val461Met(p.V461M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000392213
Start	35310095:35310095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531785357
CDS Mutation	c.1453C>T
AA Mutation	p.Arg485Cys(p.R485C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392213
Start	35309962:35309962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200859170
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392213
Start	35302503:35302503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200660504
CDS Mutation	c.1026G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392213
Start	35300334:35300334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392213
Start	35310076:35310076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392213
Start	35310097:35310097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392213
Start	35300232:35300232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.803delC
AA Mutation	p.Pro268ArgfsTer4(p.P268Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392213
Start	35295773:35295773(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.212delC
AA Mutation	p.Pro71ArgfsTer10(p.P71Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000392213
Start	35310549:35310549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>T
AA Mutation	p.Arg508Ter(p.R508*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000392213
Start	35310163:35310163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1519+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript