Transcript #00025539 (NM_001303256.2, MORC2 gene)

Transcript name transcript variant 1
Gene name MORC2 (MORC family CW-type zinc finger 2)
Chromosome 22
Transcript - NCBI ID NM_001303256.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001290185.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2020-07-24 15:06:21 +02:00 (CEST)
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.63A>G r.(?) p.(Thr21=)
-/. - c.63A>G r.(?) p.(Thr21=)
-?/. - c.68+4485C>T r.(=) p.(=)
+?/. - c.70A>G r.(?) p.(Thr24Ala)
+/. - c.71C>T r.(?) p.(Thr24Ile)
+/. - c.79G>A r.(?) p.(Glu27Lys)
?/. - c.79G>A r.(?) p.(Glu27Lys)
+/. - c.79G>A r.(?) p.(Glu27Lys)
+/. - c.79G>A r.(?) p.(Glu27Lys)
+/. - c.79G>A r.(?) p.(Glu27Lys)
+/. - c.79G>A r.(?) p.(Glu27Lys)
+/. - c.79G>A r.(?) p.(Glu27Lys)
+?/. - c.79G>A r.(?) p.(Glu27Lys)
-/. - c.96C>T r.(?) p.(Ala32=)
-/. - c.158-12del r.(=) p.(=)
-/. - c.226+18T>C r.(=) p.(=)
+?/. 5 c.229G>C r.(?) p.(Asp77His)
-/. - c.234T>G r.(?) p.(Ala78=)
+/. - c.260C>T r.(?) p.(Ser87Leu)
+/. - c.260C>T r.(?) p.(Ser87Leu)
+/. - c.260C>T r.(?) p.(Ser87Leu)
+/. - c.260C>T r.(?) p.(Ser87Leu)
+/. - c.260C>T r.(?) p.(Ser87Leu)
+?/. - c.263C>T r.(?) p.(Ala88Val)
?/. - c.286C>G r.(?) p.(Gln96Glu)
?/. - c.286C>G r.(?) p.(Gln96Glu)
+?/. - c.328C>T r.(?) p.(Arg110Cys)
-/. - c.378C>G r.(?) p.(Thr126=)
+/. - c.394C>T r.(?) p.(Arg132Cys)
+/. - c.394C>T r.(?) p.(Arg132Cys)
+/. - c.394C>T r.(?) p.(Arg132Cys)
+/. - c.394C>T r.(?) p.(Arg132Cys)
+/. - c.394C>T r.(?) p.(Arg132Cys)
+/. - c.394C>T r.(?) p.(Arg132Cys)
+/. - c.395G>T r.(?) p.(Arg132Leu)
-?/. - c.480C>A r.(?) p.(Asp160Glu)
?/. - c.480C>A r.(?) p.(Asp160Glu)
-?/. - c.626A>G r.(?) p.(Asn209Ser)
-?/. - c.683C>T r.(?) p.(Thr228Met)
-/. - c.699-20T>C r.(=) p.(=)
+/. - c.707A>G r.(?) p.(Glu236Gly)
+/. - c.707A>G r.(?) p.(Glu236Gly)
?/. - c.743A>G r.(?) p.(Tyr248Cys)
+?/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+?/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.754C>T r.(?) p.(Arg252Trp)
+/. - c.798G>C r.(?) p.(Arg266Ser)
?/. - c.848G>A r.(?) p.(Arg283His)
?/. - c.860G>T r.(?) p.(Arg287Leu)
?/. - c.917C>T r.(?) p.(Ala306Val)
-/. - c.966A>T r.(?) p.(Gly322=)
?/. - c.974C>T r.(?) p.(Thr325Met)
?/. - c.1118A>G r.(?) p.(Asn373Ser)
+/. - c.1164C>A r.(?) p.(Ser388Arg)
+?/. - c.1164C>G r.(?) p.(Ser388Arg)
+?/. - c.1164C>G r.(?) p.(Ser388Arg)
-?/. - c.1167A>C r.(?) p.(Arg389=)
?/. - c.1181A>G r.(?) p.(Tyr394Cys)
?/. - c.1181A>G r.(?) p.(Tyr394Cys)
+/. - c.1181A>G r.(?) p.(Tyr394Cys)
+/. - c.1181A>G r.(?) p.(Tyr394Cys)
+/. - c.1181A>G r.(?) p.(Tyr394Cys)
+/. - c.1199A>G r.(?) p.(Gln400Arg)
+?/. - c.1220G>A r.(?) p.(Cys407Tyr)
?/. - c.1235_1243dup r.(?) p.(Gly412_Val414dup)
+?/. - c.1237G>T r.(?) p.(Val413Phe)
+?/. - c.1237G>T r.(?) p.(Val413Phe)
?/. - c.1270A>G r.(?) p.(Thr424Ala)
+?/. - c.1292C>T r.(?) p.(Ala431Val)
+?/. - c.1292C>T r.(?) p.(Ala431Val)
+?/. - c.1330G>A r.(?) p.(Gly444Arg)
?/. - c.1330G>A r.(?) p.(Gly444Arg)
+?/. - c.1338C>A r.(?) p.(His446Gln)
?/. - c.1396G>C r.(?) p.(Asp466His)
-?/. - c.1413C>G r.(?) p.(Leu471=)
-/. - c.1437A>G r.(?) p.(Pro479=)
?/. - c.1447C>G r.(?) p.(Leu483Val)
-?/. - c.1473G>A r.(?) p.(Met491Ile)
-?/. - c.1499-9T>C r.(=) p.(=)
-?/. - c.1499-9T>C r.(=) p.(=)
-?/. - c.1499-3C>T r.spl? p.?
?/. - c.1603C>T r.(?) p.(Arg535Trp)
-/. - c.1737+4C>T r.spl? p.?
?/. - c.1753C>T r.(?) p.(Arg585Cys)
-?/. - c.1768C>T r.(?) p.(Leu590=)
-?/. - c.1848C>T r.(?) p.(Pro616=)
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