Transcript #00015652 (NM_020318.2, PAPPA2 gene)

Transcript name transcript variant 1
Gene name PAPPA2 (pappalysin 2)
Chromosome 1
Transcript - NCBI ID NM_020318.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_064714.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.380C>T r.(?) p.(Ala127Val)
-?/. - c.512C>G r.(?) p.(Thr171Ser)
?/. - c.516_518del r.(?) p.(Thr174del)
-?/. - c.689G>C r.(?) p.(Arg230Thr)
?/. - c.837_841delinsCC r.(?) p.(Ala280_Glu281delinsGln)
?/. - c.850C>T r.(?) p.(Arg284Trp)
?/. - c.941A>T r.(?) p.(His314Leu)
?/. - c.976C>T r.(?) p.(Arg326Cys)
-?/. - c.1032C>T r.(?) p.(Thr344=)
-?/. - c.1032C>T r.(?) p.(Thr344=)
?/. - c.1033G>A r.(?) p.(Asp345Asn)
-?/. - c.1039G>A r.(?) p.(Val347Met)
?/. - c.1072C>T r.(?) p.(Arg358Cys)
+?/. - c.1133T>C r.(?) p.(Leu378Pro)
-?/. - c.1240G>C r.(?) p.(Glu414Gln)
?/. - c.1258C>T r.(?) p.(Arg420Cys)
-?/. - c.1416T>G r.(?) p.(Asp472Glu)
-?/. - c.1475C>T r.(?) p.(Ser492Leu)
?/. - c.1559G>A r.(?) p.(Arg520Gln)
-?/. - c.1750G>A r.(?) p.(Val584Met)
+/. 3 c.1928_1929insTA r.(?) p.(Cys644Thrfs*25)
+/. 3 c.1928_1929insTA r.(?) p.Cys644Thrfs*25
?/. - c.1931G>T r.(?) p.(Cys644Phe)
-?/. - c.1944G>A r.(?) p.(Gln648=)
-?/. - c.1958G>A r.(?) p.(Arg653His)
?/. - c.1992G>A r.(?) p.(Arg664=)
?/. - c.2336A>G r.(?) p.(Lys779Arg)
?/. - c.2375C>T r.(?) p.(Thr792Ile)
-?/. - c.2390G>A r.(?) p.(Arg797His)
?/. - c.2431+46G>T r.(=) p.(=)
+?/. - c.2473C>T r.(?) p.(Arg825Ter)
?/. - c.2539C>T r.(?) p.(Pro847Ser)
-/. - c.3053C>T r.(?) p.(Ser1018Leu)
+?/. - c.3095A>T r.(?) p.(Asp1032Val)
+/. 8 c.3098C>T r.(?) p.(Ala1033Val)
+/. 8 c.3098C>T r.(?) p.Ala1033Val
-?/. - c.3230C>T r.(?) p.(Thr1077Met)
?/. - c.3236+10G>A r.(=) p.(=)
-?/. - c.3309G>A r.(?) p.(Ser1103=)
-?/. - c.3309G>A r.(?) p.(Ser1103=)
-?/. - c.3337C>T r.(?) p.(Pro1113Ser)
-?/. - c.3365+10_3365+11insG r.(=) p.(=)
-?/. - c.3650T>C r.(?) p.(Leu1217Pro)
-?/. - c.3686A>G r.(?) p.(His1229Arg)
-?/. - c.3798+8G>T r.(=) p.(=)
-/. - c.3822G>A r.(?) p.(=)
-?/. - c.4008C>G r.(?) p.(His1336Gln)
?/. - c.4063G>T r.(?) p.(Val1355Leu)
-?/. - c.4128G>C r.(?) p.(Glu1376Asp)
-?/. - c.4152-4C>T r.spl? p.?
?/. - c.4186T>C r.(?) p.(Cys1396Arg)
?/. - c.4274G>C r.(?) p.(Arg1425Thr)
?/. - c.4456C>G r.(?) p.(Leu1486Val)
-?/. - c.4763G>C r.(?) p.(Gly1588Ala)
-?/. - c.4849C>A r.(?) p.(Gln1617Lys)
-?/. - c.4851G>C r.(?) p.(Gln1617His)
?/. - c.4901C>T r.(?) p.(Thr1634Ile)
-?/. - c.4970C>G r.(?) p.(Pro1657Arg)
?/. - c.5050C>T r.(?) p.(Pro1684Ser)
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