Transcript #00017849 (NM_024570.3, RNASEH2B gene)

Transcript name transcript variant 1
Gene name RNASEH2B (ribonuclease H2, subunit B)
Chromosome 13
Transcript - NCBI ID NM_024570.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_078846.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 1 c.31dup r.(?) p.(Val11Glyfs*32)
+?/+? 1 c.53T>C r.(?) p.(Phe18Ser)
+/. 1i c.64+1G>A r.spl? p.?
-?/. - c.64+8C>T r.(=) p.(=)
-?/. - c.64+8C>T r.(=) p.(=)
-?/. - c.65-14C>T r.(=) p.(=)
?/. - c.89_91del r.(?) p.(Lys30del)
+/. 2 c.128C>A r.(?) p.(Pro43His)
+/. 2 c.132T>A r.(?) p.(Cys44*)
+/. 2 c.132T>A r.(?) p.(Cys44*)
+?/+? 2i c.136_136+1insT r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+?/+? 2i c.136+1del r.spl? p.?
+/. 2i c.136+1del r.spl? p.(Gly46GlufsTer18)
-?/. - c.156G>A r.(?) p.(Leu52=)
+/. 3 c.172C>T r.(?) p.(Gln58*)
-?/. - c.173A>G r.(?) p.(Gln58Arg)
+/. 3 c.179T>G r.(?) p.(Leu60Arg)
+/. 3 c.179T>G r.(?) p.(Leu60Arg)
-/. - c.189A>G r.(?) p.(Val63=)
?/. - c.203A>G r.(?) p.(Glu68Gly)
+/. 3 c.218G>T r.(?) p.(Trp73Leu)
+?/+? 3i c.244+1G>T r.spl? p.(=)
+?/+? 3i c.244+1G>T r.spl? p.(=)
+?/+? 3i c.244+1G>T r.spl? p.(=)
+?/+? 3i c.244+1G>T r.spl? p.(=)
+/. 3i c.244+1G>T r.spl? p.?
-/. - c.245-24C>T r.(=) p.(=)
+/. 4 c.247G>A r.(?) p.(Gly83Ser)
+/. - c.253C>T r.(?) p.(Leu85Phe)
+/. 4 c.257A>G r.(?) p.(His86Arg)
+/. 4 c.257A>G r.(?) p.(His86Arg)
+/. 4 c.263C>G r.(?) p.(Ala88Gly)
?/. - c.269C>T r.(?) p.(Pro90Leu)
-/. - c.322-54T>G r.(=) p.(=)
?/. - c.322-17A>G r.(=) p.(=)
+?/. - c.322-17A>G r.(=) p.(=)
+?/. - c.356A>G r.(?) p.(Asp119Gly)
+?/. - c.356A>G r.(?) p.(Asp119Gly)
+?/+? 5 c.412C>T r.(?) p.(Leu138Phe)
+/. 5 c.412C>T r.(?) p.(Leu138Phe)
+?/. 5 c.436G>A r.spl? p.(Gly146Ser)
+?/+? 5i c.436+1G>T r.spl? p.(=)
-?/. - c.455A>G r.(?) p.(Asn152Ser)
-?/. - c.455A>G r.(?) p.(Asn152Ser)
-?/. - c.455A>G r.(?) p.(Asn152Ser)
?/. - c.469A>G r.(?) p.(Lys157Glu)
?/. - c.476G>T r.(?) p.(Ser159Ile)
+/. 6 c.476G>T r.(?) p.(Ser159Ile)
+?/. 6 c.476G>T r.(?) p.(Ser159Ile)
+/. 6 c.485A>C r.(?) p.(Lys162Thr)
+/. 6 c.485A>C r.(?) p.(Lys162Thr)
+/. 6 c.485A>C r.(?) p.(Lys162Thr)
+/. 6 c.485A>C r.(?) p.(Lys162Thr)
+/. 6 c.488C>T r.(?) p.(Thr163Ile)
+/. 6 c.488C>T r.(?) p.(Thr163Ile)
+/. 6 c.488C>T r.(?) p.(Thr163Ile)
+/. 6 c.488C>T r.(?) p.(Thr163Ile)
+/. 6 c.488C>T r.(?) p.(Thr163Ile)
+?/. 6 c.498G>T r.(?) p.(Trp166Cys)
+?/. - c.509A>G r.(?) p.(Lys170Arg)
+?/+? 6i c.510+1G>A r.spl? p.(=)
+?/+? 6i c.510+1G>A r.spl? p.(=)
+/. - c.510+1G>A r.spl p.?
-?/. - c.510+6G>T r.(=) p.(=)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+?/. 13 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+?/+? 7 c.529G>A r.(?) p.(Ala177Thr)
+/. - c.529G>A r.(?) p.(Ala177Thr)
+/. - c.529G>A r.(?) p.(Ala177Thr)
+/. - c.529G>A r.(?) p.(Ala177Thr)
+/. 7 c.529G>A r.(?) p.(Ala177Thr)
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