Mutation

Primary Site >> Stomach Cancer

Gene >> GEMIN4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319004
Start	747633:747633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410G>A
AA Mutation	p.Cys137Tyr(p.C137Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319004
Start	747804:747804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370389257
CDS Mutation	c.239C>T
AA Mutation	p.Pro80Leu(p.P80L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319004
Start	746991:746991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052G>A
AA Mutation	p.Ser351Asn(p.S351N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319004
Start	747711:747711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332T>C
AA Mutation	p.Ile111Thr(p.I111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319004
Start	746064:746064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979T>G
AA Mutation	p.Leu660Trp(p.L660W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319004
Start	746384:746384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1659C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319004
Start	747380:747380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376833925
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319004
Start	747475:747475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319004
Start	746726:746726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319004
Start	747058:747058(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.985delG
AA Mutation	p.Glu329ArgfsTer24(p.E329Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript