Transcript #00014620 (NM_033004.3, NLRP1 gene)

Transcript name transcript variant 1
Gene name NLRP1 (NLR family, pyrin domain containing 1)
Chromosome 17
Transcript - NCBI ID NM_033004.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_127497.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

92 entries on 1 page. Showing entries 1 - 92.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.10G>A r.(?) p.(Gly4Arg)
?/. - c.23G>A r.(?) p.(Arg8His)
-?/. - c.57G>A r.(?) p.(=)
-?/. - c.88A>G r.(?) p.(Asn30Asp)
-?/. - c.117T>G r.(?) p.(Gly39=)
-?/. - c.144G>T r.(?) p.(Thr48=)
-?/. - c.272-7C>G r.(=) p.(=)
-?/. - c.395C>G r.(?) p.(Ser132*)
-?/. - c.449-9T>C r.(=) p.(=)
-?/. - c.636A>C r.(?) p.(Ser212=)
-?/. - c.652+7C>T r.(=) p.(=)
?/. - c.731C>T r.(?) p.(Ala244Val)
-?/. - c.736A>G r.(?) p.(Thr246Ala)
?/. - c.758A>G r.(?) p.(His253Arg)
-?/. - c.822T>G r.(?) p.(Phe274Leu)
-/. - c.847C>T r.(?) p.(Leu283Phe)
-?/. - c.923G>A r.(?) p.(Arg308Gln)
-?/. - c.923G>A r.(?) p.(Arg308Gln)
-?/. - c.1032C>T r.(?) p.(Ala344=)
-?/. - c.1103G>C r.(?) p.(Ser368Thr)
-?/. - c.1163G>A r.(?) p.(Gly388Glu)
-?/. - c.1174C>G r.(?) p.(Pro392Ala)
?/. - c.1190A>C r.(?) p.(Gln397Pro)
-?/. - c.1206A>T r.(?) p.(Pro402=)
-?/. - c.1206A>T r.(?) p.(Pro402=)
?/. - c.1249T>C r.(?) p.(Trp417Arg)
-?/. - c.1342A>G r.(?) p.(Ile448Val)
?/. - c.1377del r.(?) p.(Thr460ProfsTer17)
-?/. - c.1599G>T r.(?) p.(Gln533His)
-?/. - c.1599G>T r.(?) p.(Gln533His)
-?/. - c.1599G>T r.(?) p.(Gln533His)
-?/. - c.1658A>G r.(?) p.(His553Arg)
?/. - c.1748dup r.(?) p.(Thr584Aspfs*7)
?/. - c.1759A>G r.(?) p.(Ser587Gly)
-?/. - c.1803C>T r.(?) p.(Ile601=)
-?/. - c.1803C>T r.(?) p.(Ile601=)
-?/. - c.1836G>A r.(?) p.(Glu612=)
-?/. - c.1887C>A r.(?) p.(Phe629Leu)
-?/. - c.2114C>T r.(?) p.(Pro705Leu)
-?/. - c.2115G>A r.(?) p.(Pro705=)
-?/. - c.2142C>G r.(?) p.(His714Gln)
-?/. - c.2145T>C r.(?) p.(Ser715=)
-?/. - c.2187G>A r.(?) p.(Thr729=)
-?/. - c.2187G>A r.(?) p.(Thr729=)
-?/. - c.2187G>T r.(?) p.(Thr729=)
-?/. - c.2235A>G r.(?) p.(Val745=)
-?/. - c.2309T>C r.(?) p.(Ile770Thr)
-?/. - c.2318G>A r.(?) p.(Arg773Lys)
-?/. - c.2322G>A r.(?) p.(Gln774=)
-?/. - c.2341C>A r.(?) p.(Pro781Thr)
-?/. - c.2341C>A r.(?) p.(Pro781Thr)
-/. - c.2406C>T r.(?) p.(Ser802=)
-?/. - c.2406C>T r.(?) p.(Ser802=)
-?/. - c.2412C>T r.(?) p.(Leu804=)
-?/. - c.2414A>G r.(?) p.(Lys805Arg)
-?/. - c.2507G>A r.(?) p.(Arg836His)
+?/. - c.2528+1G>C r.spl? p.?
-?/. - c.2566G>A r.(?) p.(Asp856Asn)
-?/. - c.2605G>A r.(?) p.(Glu869Lys)
-?/. - c.2605G>A r.(?) p.(Glu869Lys)
?/. - c.2686C>G r.(?) p.(Leu896Val)
-?/. - c.2693G>A r.(?) p.(Arg898Gln)
?/. - c.2812G>T r.(?) p.(Gly938Cys)
-?/. - c.2818C>A r.(?) p.(Arg940=)
-?/. - c.2871-10G>A r.(=) p.(=)
-?/. - c.2946C>T r.(?) p.(Leu982=)
?/. - c.3004G>T r.(?) p.(Glu1002*)
-?/. - c.3096G>A r.(?) p.(Leu1032=)
-?/. - c.3134-16T>C r.(=) p.(=)
-/. - c.3205C>T r.(?) p.(His1069Tyr)
-?/. - c.3518A>G r.(?) p.(Gln1173Arg)
-?/. - c.3654C>A r.(?) p.(Leu1218=)
-?/. - c.3654C>A r.(?) p.(Leu1218=)
-?/. - c.3691G>A r.(?) p.(Val1231Ile)
-?/. - c.3703G>C r.(?) p.(Val1235Leu)
-?/. - c.3721G>A r.(?) p.(Val1241Ile)
-?/. - c.3784-4G>A r.spl? p.?
-?/. - c.3784-4G>A r.spl? p.?
?/. - c.3874G>A r.(?) p.(Val1292Met)
?/. - c.3931T>A r.(?) p.(Tyr1311Asn)
?/. - c.3964G>C r.(?) p.(Glu1322Gln)
-?/. - c.3973G>A r.(?) p.(Val1325Ile)
-?/. - c.3973G>A r.(?) p.(Val1325Ile)
?/. - c.4057G>T r.(?) p.(Gly1353Ter)
+?/. - c.4057G>T r.(?) p.(Gly1353Ter)
-?/. - c.4058-18A>T r.(=) p.(=)
-?/. - c.4102+18G>A r.(=) p.(=)
-?/. - c.4128G>A r.(?) p.(Pro1376=)
-?/. - c.4128G>A r.(?) p.(Pro1376=)
-?/. - c.4191G>A r.(?) p.(Glu1397=)
-?/. - c.4239C>T r.(?) p.(Tyr1413=)
-?/. - c.4266G>A r.(?) p.(Arg1422=)
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