Mutation

Primary Site >> Stomach Cancer

Gene >> STAU1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49117845:49117845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146630196
CDS Mutation	c.1441G>A
AA Mutation	p.Val481Ile(p.V481I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49166068:49166068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.134A>T
AA Mutation	p.Glu45Val(p.E45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49166123:49166123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79C>T
AA Mutation	p.Leu27Phe(p.L27F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49123117:49123117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200245504
CDS Mutation	c.941C>T
AA Mutation	p.Pro314Leu(p.P314L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49124559:49124559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638T>C
AA Mutation	p.Met213Thr(p.M213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49115814:49115814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1686G>T
AA Mutation	p.Glu562Asp(p.E562D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49118071:49118071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1215G>A
AA Mutation	p.Met405Ile(p.M405I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49118020:49118020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367918829
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49117858:49117858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49124579:49124579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371856
Start	49123162:49123162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.896delA
AA Mutation	p.Lys299ArgfsTer22(p.K299Rfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript