Mutation

Primary Site >> Stomach Cancer

Gene >> MGAT5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134349845:134349845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153G>A
AA Mutation	p.Glu385Lys(p.E385K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134341631:134341631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849T>G
AA Mutation	p.Phe283Leu(p.F283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134448714:134448714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2093A>C
AA Mutation	p.Lys698Thr(p.K698T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281923
Start	134428389:134428389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1819T>A
AA Mutation	p.Phe607Ile(p.F607I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134412895:134412895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146797944
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134338294:134338294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749154809
CDS Mutation	c.681T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134338354:134338354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751746374
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281923
Start	134428397:134428397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146926321
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281923
Start	134254449:134254449(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.50delT
AA Mutation	p.Phe17SerfsTer3(p.F17Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281923
Start	134318718:134318718(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.558delT
AA Mutation	p.Phe186LeufsTer43(p.F186Lfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000281923
Start	134344955:134344955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Ter(p.R335*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript