Mutation

Primary Site >> Pancreatic Cancer

Gene >> LRP1B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140540985:140540985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7501A>C
AA Mutation	p.Asn2501His(p.N2501H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	141013669:141013669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2267A>T
AA Mutation	p.Tyr756Phe(p.Y756F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140274555:140274555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13011T>G
AA Mutation	p.Ile4337Met(p.I4337M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140356394:140356394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11478C>A
AA Mutation	p.Phe3826Leu(p.F3826L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140450601:140450601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10024T>C
AA Mutation	p.Cys3342Arg(p.C3342R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140457480:140457480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9797C>A
AA Mutation	p.Ser3266Tyr(p.S3266Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140485377:140485377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9391T>A
AA Mutation	p.Phe3131Ile(p.F3131I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140495699:140495699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8900T>G
AA Mutation	p.Val2967Gly(p.V2967G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140601597:140601597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6842A>G
AA Mutation	p.Asp2281Gly(p.D2281G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140776183:140776183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5415A>C
AA Mutation	p.Lys1805Asn(p.K1805N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140850299:140850299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148341635
CDS Mutation	c.4742G>A
AA Mutation	p.Arg1581His(p.R1581H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389484
Start	140884019:140884019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751929692
CDS Mutation	c.3967G>A
AA Mutation	p.Val1323Ile(p.V1323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140989643:140989643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2659C>T
AA Mutation	p.Pro887Ser(p.P887S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	141049121:141049121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1654A>G
AA Mutation	p.Ile552Val(p.I552V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000389484
Start	140883879:140883879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4107A>T
AA Mutation	p.Arg1369Ser(p.R1369S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389484
Start	140776177:140776177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766962852
CDS Mutation	c.5421C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389484
Start	140506803:140506803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139084384
CDS Mutation	c.8514G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389484
Start	140525971:140525971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7899C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389484
Start	140908004:140908004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3393T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389484
Start	140442547:140442547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10371C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000389484
Start	140700331:140700331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6718C>T
AA Mutation	p.Arg2240Ter(p.R2240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000389484
Start	140487670:140487670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9190C>T
AA Mutation	p.Arg3064Ter(p.R3064*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript