Mutation

Primary Site >> Stomach Cancer

Gene >> MDGA2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46957578:46957578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1678A>C
AA Mutation	p.Ser560Arg(p.S560R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46920029:46920029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014C>T
AA Mutation	p.Arg672Trp(p.R672W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46873540:46873540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2438C>A
AA Mutation	p.Ala813Asp(p.A813D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46873564:46873564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2414G>A
AA Mutation	p.Arg805Gln(p.R805Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46845790:46845790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2758G>A
AA Mutation	p.Ala920Thr(p.A920T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46920118:46920118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925C>A
AA Mutation	p.Pro642Gln(p.P642Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	47131815:47131815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617T>G
AA Mutation	p.Leu206Arg(p.L206R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46873456:46873456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2522A>G
AA Mutation	p.Tyr841Cys(p.Y841C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	47131737:47131737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>T
AA Mutation	p.Ser232Leu(p.S232L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46957617:46957617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639T>G
AA Mutation	p.Leu547Val(p.L547V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46845800:46845800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2748A>C
AA Mutation	p.Glu916Asp(p.E916D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	47131746:47131746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>C
AA Mutation	p.Lys229Thr(p.K229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46841941:46841941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2861C>A
AA Mutation	p.Pro954His(p.P954H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399232
Start	46957494:46957494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1762T>C
AA Mutation	p.Phe588Leu(p.F588L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399232
Start	47061325:47061325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774276862
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399232
Start	46957468:46957468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368219229
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399232
Start	46957615:46957615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1641G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399232
Start	47061363:47061363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399232
Start	47061568:47061568(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.999delA
AA Mutation	p.Gly334AspfsTer22(p.G334Dfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399232
Start	47061568:47061569(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.998_999delAA
AA Mutation	p.Lys333ArgfsTer14(p.K333Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000399232
Start	46874198:46874198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2233G>T
AA Mutation	p.Glu745Ter(p.E745*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399232
Start	47096876:47096877(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.965dupA
AA Mutation	p.Ser323ValfsTer25(p.S323Vfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000399232
Start	46845765:46845765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2782+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript