Mutation

Primary Site >> Pancreatic Cancer

Gene >> DICER1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106152:95106152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2876A>T
AA Mutation	p.Lys959Ile(p.K959I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95093976:95093976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144259142
CDS Mutation	c.5276A>G
AA Mutation	p.Lys1759Arg(p.K1759R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95099883:95099883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4103G>A
AA Mutation	p.Arg1368His(p.R1368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95103650:95103650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3746A>C
AA Mutation	p.Lys1249Thr(p.K1249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95105102:95105102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3238G>A
AA Mutation	p.Val1080Met(p.V1080M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95106197:95106197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944Gln(p.R944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95130168:95130168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745802492
CDS Mutation	c.463G>A
AA Mutation	p.Ala155Thr(p.A155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343455
Start	95124496:95124496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076G>A
AA Mutation	p.Cys359Tyr(p.C359Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343455
Start	95115738:95115738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000343455
Start	95124590:95124590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982G>T
AA Mutation	p.Glu328Ter(p.E328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript