Mutation

Primary Site >> Stomach Cancer

Gene >> GLS

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190910308:190910308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025C>A
AA Mutation	p.Thr342Asn(p.T342N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190953570:190953570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656G>T
AA Mutation	p.Lys552Asn(p.K552N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190895238:190895238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473A>C
AA Mutation	p.Lys158Thr(p.K158T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190927330:190927330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273G>A
AA Mutation	p.Glu425Lys(p.E425K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190931604:190931604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1617A>T
AA Mutation	p.Lys539Asn(p.K539N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190931615:190931615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1628G>A
AA Mutation	p.Arg543Gln(p.R543Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320717
Start	190895626:190895626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773887348
CDS Mutation	c.506G>A
AA Mutation	p.Arg169Gln(p.R169Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320717
Start	190921154:190921154(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1085delT
AA Mutation	p.Leu362Ter(p.L362*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000320717
Start	190954662:190954662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript