Transcript #00009143

Transcript name transcript variant C
Gene name LAMP2 (lysosomal-associated membrane protein 2)
Chromosome X
Transcript - NCBI ID NM_001122606.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001116078.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

57 entries on 1 page. Showing entries 1 - 57.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-33C>T r.(=) p.(=)
?/? c.-23_-15del r.(=) p.(=)
?/? c.-10C>T r.(=) p.(=)
?/? c.-4G>C r.(=) p.(=)
?/? c.34T>A r.(?) p.(Ser12Thr)
?/? c.64+33C>T r.(=) p.(=)
?/? c.65-22T>C r.(=) p.(=)
?/? c.94A>G r.(?) p.(Asn32Asp)
?/? c.156A>T r.(=) p.(=)
?/? c.204C>G r.(?) p.(Asp68Glu)
?/? c.253G>A r.(?) p.(Gly85Ser)
?/? c.339C>T r.(=) p.(=)
?/? c.340G>A r.(?) p.(Val114Ile)
?/? c.385G>A r.(?) p.(Ala129Thr)
?/? c.415G>A r.(?) p.(Glu139Lys)
?/? c.472A>G r.(?) p.(Thr158Ala)
?/? c.504C>T r.(=) p.(=)
?/? c.515T>C r.(?) p.(Leu172Pro)
?/? c.517G>A r.(?) p.(Val173Ile)
?/? c.557-36G>A r.(=) p.(=)
?/? c.586A>T r.(?) p.(Thr196Ser)
?/? c.591G>A r.(=) p.(=)
?/? c.661G>A r.(?) p.(Gly221Arg)
?/? c.755T>G r.(?) p.(Ile252Ser)
?/? c.769A>G r.(?) p.(Asn257Asp)
?/? c.771T>C r.(=) p.(=)
?/? c.823A>G r.(?) p.(Asn275Asp)
?/? c.850T>C r.(?) p.(Phe284Leu)
?/? c.864+46C>T r.(=) p.(=)
?/? c.865-46A>G r.(=) p.(=)
?/? c.865-38G>A r.(=) p.(=)
?/? c.927C>T r.(=) p.(=)
?/? c.928+29G>T r.(=) p.(=)
?/? c.929-35A>T r.(=) p.(=)
?/? c.929-5T>C r.spl? p.?
?/? c.960C>T r.(=) p.(=)
?/? c.1003C>G r.(?) p.(Gln335Glu)
?/? c.1084T>C r.(?) p.(Tyr362His)
?/? c.1093+5G>A r.spl? p.?
?/? c.1093+9C>T r.(=) p.(=)
?/? c.1093+2416C>T r.(=) p.(=)
?/? c.1093+2450G>A r.(=) p.(=)
?/? c.1093+2478A>G r.(=) p.(=)
?/? c.1093+2513C>T r.(=) p.(=)
?/? c.1093+2514G>A r.(=) p.(=)
?/? c.1093+2531C>T r.(=) p.(=)
?/? c.1093+2568A>T r.(=) p.(=)
?/? c.1093+2589C>T r.(=) p.(=)
?/? c.1094-2813_1094-2811del r.(=) p.(=)
?/? c.1094-2788T>C r.(=) p.(=)
?/? c.1094-2768G>T r.(=) p.(=)
?/? c.1094-2682T>C r.(=) p.(=)
?/? c.1143A>G r.(=) p.(=)
?/? c.1177G>T r.(?) p.(Val393Phe)
?/? c.1191T>C r.(=) p.(=)
?/? c.1213C>A r.(?) p.(Arg405Ser)
?/? c.*34A>G r.(=) p.(=)
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