Mutation

Primary Site >> Stomach Cancer

Gene >> HLX

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220884343:220884343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754490132
CDS Mutation	c.1106G>A
AA Mutation	p.Arg369His(p.R369H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220884375:220884375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138G>A
AA Mutation	p.Asp380Asn(p.D380N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220884477:220884477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370407346
CDS Mutation	c.1240G>A
AA Mutation	p.Ala414Thr(p.A414T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220879994:220879994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137T>C
AA Mutation	p.Ile46Thr(p.I46T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220884519:220884519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>A
AA Mutation	p.Gly428Ser(p.G428S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220881267:220881267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666G>T
AA Mutation	p.Gln222His(p.Q222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220881235:220881235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634C>T
AA Mutation	p.His212Tyr(p.H212Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366903
Start	220884583:220884583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346C>T
AA Mutation	p.Ala449Val(p.A449V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366903
Start	220879881:220879881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366903
Start	220884293:220884293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366903
Start	220880184:220880184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366903
Start	220884347:220884347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1110T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366903
Start	220881291:220881291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755377116
CDS Mutation	c.690T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366903
Start	220880028:220880028(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.175delG
AA Mutation	p.Ala59ArgfsTer138(p.A59Rfs*138)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000366903
Start	220880041:220880041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>T
AA Mutation	p.Glu62Ter(p.E62*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000366903
Start	220884217:220884218(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.982_987dupCGGATG
AA Mutation	p.Arg328_Met329dup(p.R328_M329dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript