Transcript #00024229 (NM_033109.4, PNPT1 gene)

Transcript name polyribonucleotide nucleotidyltransferase 1
Gene name PNPT1 (polyribonucleotide nucleotidyltransferase 1)
Chromosome 2
Transcript - NCBI ID NM_033109.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_149100.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-02-19 11:18:42 +01:00 (CET)
Date last edited N/A


Variants

75 entries on 1 page. Showing entries 1 - 75.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-6160223_*28262964dup r.0? p.0?
?/. - c.77G>A r.(?) p.(Arg26Gln)
-?/. - c.122G>C r.(?) p.(Ser41Thr)
+/. - c.137C>G r.(?) p.(Ala46Gly)
+/. - c.208T>C r.(?) p.(Ser70Pro)
?/. - c.222+3A>C r.spl? p.?
-?/. - c.223-9A>T r.(=) p.(=)
?/. - c.269C>G r.(?) p.(Pro90Arg)
+?/+? 4 c.350T>C r.(?) p.(Leu117Pro)
-/. - c.361A>G r.(?) p.(Ile121Val)
+/+ 4 c.394C>T r.(?) p.(Arg132*)
+/. - c.404-1G>A r.spl p.?
?/? 4i c.404-1G>A r.spl? p.?
+/. - c.407G>A r.(?) p.(Arg136His)
+?/. 5 c.407G>A r.(?) p.(Arg136His)
-?/. - c.412A>G r.(?) p.(Ile138Val)
+?/. 5 c.419C>T r.(?) p.(Pro140Leu)
-?/. - c.453+10_453+11insAG r.(=) p.(=)
?/. - c.472G>T r.(?) p.(Ala158Ser)
-?/. - c.493C>T r.(?) p.(Pro165Ser)
+?/+? 6 c.493C>T r.(?) p.(Pro165Ser)
./. - c.562G>C r.(?) p.(Val188Leu)
-?/. - c.566-6T>C r.(=) p.(=)
?/. - c.568G>T r.(?) p.(Ala190Ser)
+?/+? 8 c.575G>A r.(?) p.(Arg192Gln)
?/. - c.587T>C r.(?) p.(Ile196Thr)
-?/. - c.622G>C r.(?) p.(Glu208Gln)
-?/. - c.667A>G r.(?) p.(Lys223Glu)
-?/. - c.789A>G r.(?) p.(Val263=)
-?/. - c.852G>C r.(?) p.(Val284=)
-?/. - c.862C>T r.(?) p.(His288Tyr)
+?/+? 10 c.887A>G r.(?) p.(Tyr296Cys)
-?/. - c.1051A>G r.(?) p.(Ile351Val)
-/. - c.1074-19A>G r.(=) p.(=)
-?/. - c.1074-4A>T r.spl? p.?
+/+ 13 c.1160A>G r.(?) p.(Gln387Arg)
-?/. - c.1176+7del r.(=) p.(=)
?/. - c.1189G>A r.(?) p.(Val397Ile)
?/. - c.1228C>G r.(?) p.(Gln410Glu)
-?/. - c.1231G>A r.(?) p.(Val411Ile)
-?/. - c.1251G>A r.(?) p.(Gly417=)
-/. - c.1285-4del r.spl? p.?
-/. - c.1390C>A r.(?) p.(Arg464=)
+/. - c.1399C>T r.(?) p.(Pro467Ser)
?/. - c.1414G>A r.(?) p.(Val472Ile)
+/+ 17 c.1424A>G r.(?) p.(Glu475Gly)
+?/. - c.1453A>G r.(?) p.(Met485Val)
+/+ 18 c.1453A>G r.(?) p.(Met485Val)
+/. - c.1495G>A r.(?) p.(Gly499Arg)
+?/. - c.1519G>T r.(?) p.(Ala507Ser)
+/. - c.1519G>T r.(?) p.(Ala507Ser)
+/. - c.1519G>T r.(?) p.(Ala507Ser)
+?/+? 19 c.1519G>T r.(?) p.(Ala507Ser)
+/. - c.1525G>A r.(?) p.(Val509Ile)
+?/+? 19 c.1525G>A r.(?) p.(Val509Ile)
+/. - c.1579_1580insGAT r.(?) p.(Tyr527Ter)
?/. - c.1582C>A r.(?) p.(Arg528Ser)
+?/. - c.1592C>G r.(?) p.(Thr531Arg)
+/. - c.1592C>G r.(?) p.(Thr531Arg)
+?/+? 19 c.1592C>G r.(?) p.(Thr531Arg)
+/. - c.1619A>G r.(?) p.(Asn540Ser)
?/. - c.1676C>G r.(?) p.(Ala559Gly)
-?/. - c.1929T>C r.(?) p.(Asp643=)
-?/. - c.1938G>A r.(?) p.(Thr646=)
?/. - c.1972C>T r.(?) p.(His658Tyr)
+?/+? 25 c.2050G>A r.(?) p.(Ala684Thr)
?/. - c.2068A>C r.(?) p.(=)
-?/. - c.2070-5T>C r.spl? p.?
+/. - c.2137G>T r.(?) p.(Asp713Tyr)
-?/. - c.2149-5dup r.spl? p.?
?/. - c.2185C>A r.(?) p.(Gln729Lys)
?/. - c.2213G>A r.(?) p.(Arg738His)
-?/. - c.2247A>G r.(?) p.(Arg749=)
?/. - c.2275G>A r.(?) p.(Val759Met)
-/. - c.*11dup r.(?) p.(=)
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