Transcript #00016220 (NM_031220.3, PITPNM3 gene)

Transcript name transcript variant 1
Gene name PITPNM3 (PITPNM family member 3)
Chromosome 17
Transcript - NCBI ID NM_031220.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_112497.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. 16 c.? r.(?) p.?
?/. - c.16C>T r.(?) p.(Arg6Cys)
-?/. - c.16C>T r.(?) p.(Arg6Cys)
-?/. - c.22+15G>C r.(=) p.(=)
-?/. - c.42C>T r.(?) p.(Gly14=)
+?/. - c.55C>T r.(?) p.(His19Tyr)
-?/. - c.62G>A r.(?) p.(Arg21Gln)
?/. - c.176A>G r.(?) p.(Asn59Ser)
-?/. - c.201C>T r.(?) p.(Thr67=)
-?/. - c.216C>T r.(?) p.(Asp72=)
-?/. - c.216C>T r.(?) p.(Asp72=)
-/. - c.226+9C>G r.(=) p.(=)
-/. - c.238G>A r.(?) p.(Ala80Thr)
?/. 4 c.239C>T r.(?) p.(Ala80Val)
+/. - c.274C>T r.(?) p.(Arg92*)
?/. - c.287G>A r.(?) p.(Arg96Gln)
-?/. - c.287G>A r.(?) p.(Arg96Gln)
?/. 5 c.296T>C r.(?) p.(Leu99Ser)
-?/. - c.330C>T r.(?) p.(Ile110=)
-?/. - c.330C>T r.(?) p.(Ile110=)
?/. - c.334A>G r.(?) p.(Ile112Val)
-?/. - c.339C>T r.(?) p.(=)
-?/. - c.349G>A r.(?) p.(Glu117Lys)
-?/. - c.351+15G>A r.(=) p.(=)
-/. - c.432C>T r.(?) p.(Ala144=)
-?/. - c.477C>T r.(?) p.(Ser159=)
?/. - c.503A>G r.(?) p.(His168Arg)
?/. - c.527T>C r.(?) p.(Ile176Thr)
-?/. - c.576G>A r.(?) p.(Ser192=)
+?/. 6 c.687C>G r.(?) p.(Tyr229*)
-?/. - c.699C>T r.(?) p.(Val233=)
?/. - c.700G>A r.(?) p.(Ala234Thr)
-?/. - c.747G>A r.(?) p.(Lys249=)
?/. - c.775C>A r.(?) p.(Gln259Lys)
-?/. - c.789C>T r.(?) p.(Ile263=)
-?/. - c.838G>A r.(?) p.(Ala280Thr)
-/. - c.849A>G r.(?) p.(Ser283=)
-?/. - c.849A>G r.(?) p.(Ser283=)
-?/. - c.879G>A r.(?) p.(=)
?/. - c.900+60C>T r.(?) p.(=)
?/. - c.901-45G>A r.(?) p.(=)
-?/. - c.901-9G>A r.(=) p.(=)
-?/. - c.914C>T r.(?) p.(Ala305Val)
-?/. - c.987G>A r.(?) p.(Leu329=)
-?/. - c.987G>A r.(?) p.(Leu329=)
-?/. - c.1016C>G r.(?) p.(Pro339Arg)
+/. - c.1025A>C r.(?) p.(Gln342Pro)
?/. - c.1057A>G r.(?) p.(Ile353Val)
-?/. - c.1085+8del r.(=) p.(=)
-?/. - c.1125G>A r.(?) p.(=)
-?/. - c.1128G>A r.(?) p.(Ala376=)
-?/. - c.1128G>A r.(?) p.(Ala376=)
-?/. - c.1139C>T r.(?) p.(Pro380Leu)
-?/. - c.1179T>C r.(?) p.(Asp393=)
-/. - c.1308C>T r.(?) p.(Cys436=)
?/. 11 c.1395G>C r.(?) p.(Arg465Ser)
-/. - c.1477C>T r.(?) p.(Arg493Trp)
-/. - c.1512G>A r.(?) p.(Ser504=)
-/. - c.1538G>A r.(?) p.(Arg513His)
-?/. - c.1584G>A r.(?) p.(Ser528=)
-?/. - c.1593G>A r.(?) p.(Ser531=)
-?/. - c.1599C>T r.(?) p.(Ser533=)
?/. 12 c.1601T>A r.(?) p.(Met534Lys)
?/. - c.1656C>G r.(?) p.(Ile552Met)
+?/. - c.1657_1660dup r.(?) p.(Tyr554*)
?/. - c.1671C>T r.(?) p.(Tyr557=)
-?/. - c.1683C>T r.(?) p.(Val561=)
?/. - c.1688C>T r.(?) p.(Thr563Met)
?/. - c.1688C>T r.(?) p.(Thr563Met)
?/. - c.1688C>T r.(?) p.(Thr563Met)
?/. - c.1688C>T r.(?) p.(Thr563Met)
-?/. - c.1701C>T r.(?) p.(Thr567=)
?/. - c.1726G>A r.(?) p.(Ala576Thr)
?/. - c.1878G>C r.(?) p.(Gln626His)
+/. - c.1878G>C r.(?) p.(Gln626His)
+/. - c.1878G>C r.(?) p.(Gln626His)
+/. - c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
?/. - c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
?/. - c.1878G>C r.(?) p.(Gln626His)
-?/. - c.1878G>C r.(?) p.(Gln626His)
-?/. - c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
+/. 14 c.1878G>C r.(?) p.(Gln626His)
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