Transcript #00014631 (NM_144687.2, NLRP12 gene)

Transcript name transcript variant 2
Gene name NLRP12 (NLR family, pyrin domain containing 12)
Chromosome 19
Transcript - NCBI ID NM_144687.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_653288.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

116 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-140T>A r.(?) p.(=)
-/. - c.-12C>T r.(?) p.(=)
-/. - c.-12C>T r.(?) p.(=)
-?/. - c.14C>A r.(?) p.(Ala5Glu)
?/. - c.29T>C r.(?) p.(Leu10Pro)
-/. - c.116G>T r.(?) p.(Gly39Val)
-?/. - c.236G>A r.(?) p.(Arg79Gln)
-/. - c.289+18C>T r.(=) p.(=)
-?/. - c.291T>C r.(?) p.(Asp97=)
-?/. - c.308C>T r.(?) p.(Pro103Leu)
-/. - c.370+162C>G r.(=) p.(=)
-?/. - c.371-63C>T r.(=) p.(=)
?/. - c.373C>A r.(?) p.(Pro125Thr)
-?/. - c.391G>A r.(?) p.(Asp131Asn)
-?/. - c.420G>A r.(?) p.(Met140Ile)
-/. - c.424G>A r.(?) p.(Asp142Asn)
-/. - c.424G>A r.(?) p.(Asp142Asn)
+?/. - c.430A>G r.(?) p.(Asn144Asp)
-?/. - c.436C>T r.(?) p.(Arg146Cys)
-?/. - c.539G>A r.(?) p.(Gly180Asp)
?/. - c.617G>A r.(?) p.(Arg206His)
-?/. - c.752A>G r.(?) p.(Asn251Ser)
?/. - c.779C>T r.(?) p.(Thr260Met)
-?/. - c.779C>T r.(?) p.(Thr260Met)
+/. - c.788_794dup r.(?) p.(Asp266Hisfs*11)
?/. - c.794A>G r.(?) p.(Gln265Arg)
-?/. - c.819T>C r.(?) p.(Pro273=)
?/. - c.850C>T r.(?) p.(Arg284*)
?/. - c.857C>T r.(?) p.(Pro286Leu)
-?/. - c.858C>T r.(?) p.(Pro286=)
-?/. - c.910C>T r.(?) p.(His304Tyr)
-?/. - c.910C>T r.(?) p.(His304Tyr)
-/. - c.956C>G r.(?) p.(Pro319Arg)
-/. - c.956C>G r.(?) p.(Pro319Arg)
-/. - c.969T>G r.(?) p.(Leu323=)
-?/. - c.986G>A r.(?) p.(Arg329Gln)
?/. - c.1054C>T r.(?) p.(Arg352Cys)
?/. - c.1054C>T r.(?) p.(Arg352Cys)
?/. - c.1054C>T r.(?) p.(Arg352Cys)
?/. - c.1054C>T r.(?) p.(Arg352Cys)
-?/. - c.1137C>T r.(?) p.(His379=)
+/. - c.1170C>A r.(?) p.(Tyr390*)
-/. - c.1206C>G r.(?) p.(Phe402Leu)
?/. - c.1230G>A r.(?) p.(Val410=)
-?/. - c.1299A>G r.(?) p.(Ala433=)
-/. - c.1347C>G r.(?) p.(Ala449=)
-?/. - c.1352G>A r.(?) p.(Arg451His)
?/. - c.1568C>G r.(?) p.(Ala523Gly)
-?/. - c.1587C>G r.(?) p.(Asp529Glu)
-?/. - c.1731G>A r.(?) p.(Lys577=)
?/. - c.1923T>G r.(?) p.(Ile641Met)
?/. - c.2026G>A r.(?) p.(Asp676Asn)
?/. - c.2072+2dup r.spl? p.?
+?/. - c.2072+2dup r.spl? p.?
-?/. - c.2072+12T>G r.(=) p.(=)
-?/. - c.2072+16G>T r.(=) p.(=)
?/. - c.2078A>G r.(?) p.(Glu693Gly)
-?/. - c.2141A>G r.(?) p.(Asn714Ser)
-?/. - c.2141A>G r.(?) p.(Asn714Ser)
-?/. - c.2165G>A r.(?) p.(Arg722Gln)
?/. - c.2182C>T r.(?) p.(Arg728Trp)
?/. - c.2185G>C r.(?) p.(Gly729Arg)
?/. - c.2243+2T>C r.spl? p.?
-/. - c.2244-345C>T r.(=) p.(=)
-/. - c.2244-233G>T r.(=) p.(=)
-?/. - c.2345T>C r.(?) p.(Val782Ala)
-?/. - c.2383C>A r.(?) p.(Arg795=)
?/. - c.2386del r.(?) p.(His796Ilefs*8)
-/. - c.2394= r.(=) p.(Gln798=)
-?/. - c.2414+16C>T r.(=) p.(=)
-?/. - c.2415-8C>T r.(=) p.(=)
-?/. - c.2439C>T r.(?) p.(Ser813=)
-/. - c.2469C>A r.(?) p.(Leu823=)
-/. - c.2469C>T r.(?) p.(Leu823=)
-?/. - c.2471G>T r.(?) p.(Gly824Val)
?/. - c.2486T>C r.(?) p.(Leu829Pro)
?/. - c.2572C>A r.(?) p.(Leu858Ile)
-/. - c.2576G>A r.(?) p.(Arg859Gln)
-?/. - c.2579C>G r.(?) p.(Thr860Ser)
-?/. - c.2600G>A r.(?) p.(Arg867His)
-?/. - c.2622C>T r.(?) p.(Asp874=)
?/. - c.2638C>G r.(?) p.(Leu880Val)
-/. - c.2701G>C r.(?) p.(Val901Leu)
?/. - c.2753T>C r.(?) p.(Leu918Pro)
-/. - c.2754G>C r.(?) p.(Leu918=)
-/. - c.2755C>T r.(?) p.(Arg919Trp)
-/. - c.2755C>T r.(?) p.(Arg919Trp)
-?/. - c.2761G>C r.(?) p.(Gly921Arg)
?/. - c.2770C>T r.(?) p.(Arg924Trp)
-?/. - c.2784C>T r.(?) p.(Ala928=)
-/. - c.2830C>A r.(?) p.(Arg944=)
-?/. - c.2830C>A r.(?) p.(Arg944=)
-?/. - c.2830C>A r.(?) p.(Arg944=)
?/. - c.2830C>T r.(?) p.(Arg944Trp)
+?/. - c.2877G>A r.(?) p.(Trp959Ter)
-?/. - c.2905G>A r.(?) p.(Ala969Thr)
?/. - c.2912G>C r.(?) p.(Arg971Thr)
-?/. - c.2927+4_2927+5dup r.spl? p.?
-?/. - c.2927+4_2927+5dup r.spl? p.?
-/. - c.2927+11G>A r.(=) p.(=)
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