Mutation

Primary Site >> Pancreatic Cancer

Gene >> ARID1A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26732705:26732705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1833G>T
AA Mutation	p.Gln611His(p.Q611H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26774528:26774528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4301C>T
AA Mutation	p.Ala1434Val(p.A1434V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324856
Start	26779296:26779296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551963483
CDS Mutation	c.5398A>T
AA Mutation	p.Asn1800Tyr(p.N1800Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26779674:26779674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5777delG
AA Mutation	p.Gly1926GlufsTer30(p.G1926Efs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26731579:26731579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1780delC
AA Mutation	p.Gln594SerfsTer25(p.Q594Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26779687:26779687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5789delC
AA Mutation	p.Ser1930Ter(p.S1930*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26773459:26773459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3829C>T
AA Mutation	p.Gln1277Ter(p.Q1277*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26773456:26773456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3826C>T
AA Mutation	p.Arg1276Ter(p.R1276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26766246:26766246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387906845
CDS Mutation	c.2758C>T
AA Mutation	p.Gln920Ter(p.Q920*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26779737:26779737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5839C>T
AA Mutation	p.Gln1947Ter(p.Q1947*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000324856
Start	26774851:26774851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4624G>T
AA Mutation	p.Glu1542Ter(p.E1542*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324856
Start	26780721:26780722(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6825_6826dupTT
AA Mutation	p.Cys2276PhefsTer7(p.C2276Ffs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000324856
Start	26772988:26772988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3715+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript