Transcript #00016924 (NM_020719.1, PRR12 gene)

Transcript name proline rich 12
Gene name PRR12 (proline rich 12)
Chromosome 19
Transcript - NCBI ID NM_020719.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_065770.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3149G>A r.(?) p.(=)
?/. - c.-3063C>T r.(?) p.(=)
-?/. - c.-1718C>G r.(?) p.(=)
?/. - c.-1613C>T r.(?) p.(=)
?/. - c.-1612C>G r.(?) p.(=)
-?/. - c.-1285G>A r.(?) p.(=)
+/. - c.1_*832{0} r.0 p.0
-?/. - c.200-10C>A r.(=) p.(=)
?/. - c.235G>A r.(?) p.(Ala79Thr)
+/. - c.334dup r.(?) p.(Gln112Profs*69)
?/. - c.476G>A r.(?) p.(Ser159Asn)
?/. - c.511C>T r.(?) p.(Gln171*)
?/. - c.581C>T r.(?) p.(Ser194Leu)
+?/. - c.627del r.(?) p.(Gly211AlafsTer104)
?/. - c.662C>T r.(?) p.(Pro221Leu)
?/. - c.676C>A r.(?) p.(Pro226Thr)
+/. - c.677dup r.(?) p.(Tyr227Leufs*41)
?/. - c.768_770dup r.(?) p.(Ala258dup)
+/. - c.790C>T r.(?) p.(Gln264*)
+/. - c.903_909dup r.(?) p.(Pro304Thrfs*46)
-?/. - c.923A>T r.(?) p.(His308Leu)
-?/. - c.1041C>T r.(?) p.(Ser347=)
?/. - c.1049G>A r.(?) p.(Gly350Asp)
?/. - c.1054A>C r.(?) p.(Ser352Arg)
?/. - c.1067_1090del r.(?) p.(Ala356_Thr363del)
?/. - c.1091G>A r.(?) p.(Gly364Asp)
+?/. - c.1146dup r.(?) p.(Ile383HisfsTer176)
+?/. - c.1201G>A r.(?) p.(Gly401Arg)
-?/. - c.1223C>A r.(?) p.(Pro408Gln)
?/. - c.1223C>G r.(?) p.(Pro408Arg)
+/. - c.1232C>A r.(?) p.(Ser411*)
-?/. - c.1237G>A r.(?) p.(Ala413Thr)
-?/. - c.1276G>A r.(?) p.(Ala426Thr)
-?/. - c.1369T>C r.(?) p.(Tyr457His)
+/. - c.1521T>G r.(?) p.(Tyr507*)
+/. - c.1521T>G r.(?) p.(Tyr507*)
-?/. - c.1593C>G r.(?) p.(Leu531=)
?/. - c.1666G>T r.(?) p.(Gly556Cys)
?/. - c.1700C>T r.(?) p.(Pro567Leu)
-?/. - c.1904G>A r.(?) p.(Arg635His)
+/. - c.1918G>T r.(?) p.(Glu640*)
-?/. - c.1947G>A r.(?) p.(Ala649=)
?/. - c.1973C>T r.(?) p.(Ala658Val)
+/. - c.2045del r.(?) p.(Gly682Aspfs*44)
?/. - c.2201G>T r.(?) p.(Arg734Leu)
+/. - c.2236_2237del r.(?) p.(Val746Cysfs*43)
+/. - c.2353_2360del r.(?) p.(Ala785Profs*2)
+/. - c.2398dup r.(?) p.(Gln800Profs*26)
-?/. - c.2403_2405dup r.(?) p.(Leu802dup)
+/. - c.2500C>T r.(?) p.(Gln834Ter)
-?/. - c.2509_2510del r.(?) p.(Pro837Thrfs*99)
-?/. - c.2529A>G r.(?) p.(=)
-?/. - c.2530C>T r.(?) p.(Pro844Ser)
?/. - c.2554_2556del r.(?) p.(Ala852del)
+/. - c.2587dup r.(?) p.(Ala863Glyfs*74)
-?/. - c.2598C>T r.(?) p.(Pro866=)
?/. - c.2600G>A r.(?) p.(Arg867His)
-?/. - c.2600G>A r.(?) p.(Arg867His)
+/. 4 c.2641C>T r.(?) p.(Gln881*)
?/. - c.2665C>T r.(?) p.(Pro889Ser)
-?/. - c.2695G>A r.(?) p.(Val899Ile)
?/. - c.2712_2723del r.(?) p.(Glu905_Asp908del)
+/. - c.2732_2744del r.(?) p.(Gly911Alafs*115)
+/. - c.2755C>T r.(?) p.(Gln919*)
?/. - c.2823C>A r.(?) p.(Asp941Glu)
+/. - c.2824del r.(?) p.(Glu942Argfs*88)
+/. - c.3009_3028dup r.(?) p.(Leu1010Profs*27)
?/. - c.3062C>T r.(?) p.(Thr1021Met)
+/. - c.3129_3134del r.(?) p.(Pro1048_Pro1049del)
+/. - c.3224del r.(?) p.(Thr1075Asnfs*148)
-?/. - c.3269C>G r.(?) p.(Thr1090Ser)
+/. - c.3273del r.(?) p.(Lys1092Argfs*131)
+/. - c.3273del r.(?) p.(Lys1092Argfs*131)
?/. - c.3373G>A r.(?) p.(Val1125Ile)
-?/. - c.3439C>T r.(?) p.(Pro1147Ser)
?/. - c.3469C>G r.(?) p.(Arg1157Gly)
+?/. - c.3505C>T r.(?) p.(Arg1169Trp)
-?/. - c.3582C>G r.(?) p.(Thr1194=)
?/. - c.3789C>G r.(?) p.(Ile1263Met)
+/. - c.3958C>T r.(?) p.(Arg1320*)
-?/. - c.3959G>A r.(?) p.(Arg1320Gln)
?/. - c.4139_4141del r.(?) p.(Phe1380del)
?/. - c.4201G>A r.(?) p.(Ala1401Thr)
?/. - c.4387C>T r.(?) p.(Pro1463Ser)
?/. - c.4414C>T r.(?) p.(Pro1472Ser)
?/. - c.4423C>A r.(?) p.(Pro1475Thr)
-?/. - c.4423C>A r.(?) p.(Pro1475Thr)
?/. - c.4427C>T r.(?) p.(Pro1476Leu)
-?/. - c.4488A>T r.(?) p.(Pro1496=)
+/. - c.4502_4505del r.(?) p.(Leu1501Argfs*146)
-?/. - c.4533G>A r.(?) p.(=)
?/. - c.4604C>A r.(?) p.(Pro1535His)
?/. - c.4642C>G r.(?) p.(Leu1548Val)
+/. - c.4674_4676delinsGC r.(?) p.(Cys1558Trpfs*90)
+/. - c.4726G>T r.(?) p.(Glu1576*)
+/. - c.4768dup r.(?) p.(Leu1590ProfsTer10)
+/. - c.4768dup r.(?) p.(Leu1590Profs*10)
+/. - c.4891-2A>G r.spl p.?
+/. - c.5005C>T r.(?) p.(Arg1669Trp)
-?/. - c.5050G>A r.(?) p.(Val1684Ile)
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