Transcript #00016359 (NM_002666.4, PLIN1 gene)

Transcript name transcript variant 1
Gene name PLIN1 (perilipin 1)
Chromosome 15
Transcript - NCBI ID NM_002666.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_002657.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

99 entries on 1 page. Showing entries 1 - 99.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.13A>G r.(?) p.(Lys5Glu)
-?/. - c.45+20C>T r.(=) p.(=)
-?/. - c.46-12C>G r.(=) p.(=)
?/. - c.46-8C>T r.(=) p.(=)
?/. - c.46-4_50del r.spl? p.?
-?/. - c.48G>A r.(?) p.(Glu16=)
-?/. - c.107G>T r.(?) p.(Cys36Phe)
?/. - c.123C>A r.(?) p.(Tyr41*)
-?/. - c.147C>A r.(?) p.(=)
?/. - c.209C>T r.(?) p.(Ala70Val)
?/. - c.224C>T r.(?) p.(Pro75Leu)
?/. - c.233G>A r.(?) p.(Arg78His)
-?/. - c.245C>T r.(?) p.(Thr82Ile)
-/. - c.245C>T r.(?) p.(Thr82Ile)
?/. - c.335_350del r.(?) p.(Ile112Argfs*103)
?/. - c.358A>G r.(?) p.(Ile120Val)
?/. - c.365C>T r.(?) p.(Thr122Ile)
?/. - c.367C>T r.(?) p.(Arg123Cys)
?/. - c.380C>T r.(?) p.(Ala127Val)
-?/. - c.408G>A r.(?) p.(Ala136=)
-?/. - c.414T>G r.(?) p.(Thr138=)
?/. - c.445G>T r.(?) p.(Gly149Trp)
?/. - c.445G>T r.(?) p.(Gly149Trp)
-?/. - c.449G>A r.(?) p.(Cys150Tyr)
-?/. - c.466G>T r.(?) p.(Val156Leu)
-?/. - c.466G>T r.(?) p.(Val156Leu)
?/. - c.469G>A r.(?) p.(Ala157Thr)
+?/. - c.517G>A r.(?) p.(Ala173Thr)
?/. - c.561G>A r.(?) p.(Val187=)
-?/. - c.571C>A r.(?) p.(Leu191Ile)
-?/. - c.580C>A r.(?) p.(Pro194Thr)
-/. - c.580C>G r.(?) p.(Pro194Ala)
-?/. - c.598+14G>A r.(=) p.(=)
-?/. - c.599-15C>A r.(=) p.(=)
-?/. - c.644A>G r.(?) p.(Lys215Arg)
-?/. - c.692G>T r.(?) p.(Arg231Leu)
-?/. - c.739G>A r.(?) p.(Val247Met)
-?/. - c.772-9C>G r.(=) p.(=)
?/. - c.791G>A r.(?) p.(Gly264Asp)
-?/. - c.812C>T r.(?) p.(Ala271Val)
-?/. - c.814G>A r.(?) p.(Val272Met)
-?/. - c.824G>A r.(?) p.(Arg275Gln)
-?/. - c.831C>T r.(?) p.(Ser277=)
?/. - c.839G>A r.(?) p.(Arg280Gln)
-?/. - c.861C>T r.(?) p.(Leu287=)
-?/. - c.870C>T r.(?) p.(Ala290=)
-?/. - c.877G>A r.(?) p.(Glu293Lys)
?/. - c.901A>G r.(?) p.(Thr301Ala)
?/. - c.902C>T r.(?) p.(Thr301Met)
-?/. - c.902C>T r.(?) p.(Thr301Met)
?/. - c.917C>T r.(?) p.(Thr306Met)
?/. - c.961G>A r.(?) p.(Glu321Lys)
-?/. - c.963+8G>A r.(=) p.(=)
-?/. - c.975G>A r.(?) p.(Leu325=)
-?/. - c.981C>T r.(?) p.(=)
-?/. - c.986G>A r.(?) p.(Arg329Gln)
-?/. - c.990C>T r.(?) p.(Gly330=)
-?/. - c.990C>T r.(?) p.(Gly330=)
-?/. - c.1001G>A r.(?) p.(Gly334Asp)
?/. - c.1007C>T r.(?) p.(Ala336Val)
-?/. - c.1027C>T r.(?) p.(Leu343Phe)
-?/. - c.1043C>T r.(?) p.(Ser348Leu)
?/. - c.1060C>G r.(?) p.(Pro354Ala)
-/. - c.1113T>C r.(?) p.(Pro371=)
?/. - c.1138G>A r.(?) p.(Ala380Thr)
-?/. - c.1139C>T r.(?) p.(Ala380Val)
?/. - c.1154A>G r.(?) p.(Asp385Gly)
?/. - c.1168G>A r.(?) p.(Val390Ile)
-?/. - c.1179C>T r.(?) p.(Asn393=)
?/. - c.1180G>A r.(?) p.(Val394Met)
-?/. - c.1204G>A r.(?) p.(Val402Met)
-?/. - c.1204G>A r.(?) p.(Val402Met)
?/. - c.1205T>G r.(?) p.(Val402Gly)
-?/. - c.1209G>A r.(?) p.(Pro403=)
-?/. - c.1209+9C>T r.(=) p.(=)
+?/. - c.1210-13_1211del r.spl? p.?
?/. - c.1210-3C>T r.spl? p.?
-/. - c.1248C>T r.(?) p.(Phe416=)
?/. - c.1259A>G r.(?) p.(Asp420Gly)
?/. - c.1259A>G r.(?) p.(Asp420Gly)
-?/. - c.1271C>T r.(?) p.(Ala424Val)
-?/. - c.1278C>T r.(?) p.(Val426=)
-?/. - c.1281G>C r.(?) p.(Glu427Asp)
-?/. - c.1284_1286dup r.(?) p.(Arg429dup)
-?/. - c.1329G>A r.(?) p.(Pro443=)
?/. - c.1344T>C r.(?) p.(Arg448=)
-?/. - c.1358G>A r.(?) p.(Arg453His)
?/. - c.1369C>T r.(?) p.(Arg457Cys)
-?/. - c.1382G>A r.(?) p.(Ser461Asn)
-?/. - c.1383C>A r.(?) p.(Ser461Arg)
-?/. - c.1385C>T r.(?) p.(Pro462Leu)
-?/. - c.1386C>T r.(?) p.(Pro462=)
-?/. - c.1392G>T r.(?) p.(Ala464=)
?/. - c.1393C>T r.(?) p.(Pro465Ser)
-?/. - c.1393C>T r.(?) p.(Pro465Ser)
-?/. - c.1395C>A r.(?) p.(Pro465=)
?/. - c.1465C>T r.(?) p.(Arg489Cys)
?/. - c.1535G>A r.(?) p.(Arg512His)
-?/. - c.1556G>C r.(?) p.(Arg519Pro)
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