Transcript #00000015

Transcript name zinc finger protein 41, transcript variant 1
Gene name ZNF41 (zinc finger protein 41)
Chromosome X
Transcript - NCBI ID NM_007130.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_009061.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

46 entries on 1 page. Showing entries 1 - 46.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
?/. - c.-431_-430insCGCG - - p.(=)
?/. - c.-430_-429del - - p.(=)
?/. - c.-425_-424insCGCGCG - - p.(=)
?/. - c.-422_-421insGCGCGCACGC - - p.(=)
?/. - c.-307G>A - - p.(=)
?/. - c.-307G>A - - p.(=)
?/. - c.-280+78A>G - - p.(=)
?/. - c.-280+78A>G - - p.(=)
?/. - c.-231A>G - r.(=) p.(=)
-?/. - c.88G>A likely benign r.(?) p.(Glu30Lys)
?/. - c.281A>G VUS r.(?) p.(His94Arg)
-?/. - c.332C>T likely benign r.(?) p.(Pro111Leu)
-?/. - c.332C>T likely benign r.(?) p.(Pro111Leu)
?/. - c.332C>T VUS r.(?) p.(Pro111Leu)
-?/. - c.332C>T likely benign r.(?) p.(Pro111Leu)
?/. 5 c.374T>G - r.(?) p.(Ile125Arg)
?/. - c.522A>C VUS r.(?) p.(Lys174Asn)
-/. - c.590A>G benign r.(?) p.(Lys197Arg)
-?/. - c.590A>G likely benign r.(?) p.(Lys197Arg)
-?/. - c.664A>G likely benign r.(?) p.(Asn222Asp)
-/. - c.746A>C benign r.(?) p.(Glu249Ala)
?/. - c.746A>C VUS r.(?) p.(Glu249Ala)
-?/. 5 c.786G>A - r.(?) p.(=)
-?/. - c.823G>A likely benign r.(?) p.(Glu275Lys)
-?/. - c.896G>A likely benign r.(?) p.(Arg299His)
-?/. - c.901T>C likely benign r.(?) p.(Cys301Arg)
-?/. - c.945T>G likely benign r.(?) p.(Asp315Glu)
-?/. - c.945T>G likely benign r.(?) p.(Asp315Glu)
?/. 5 c.945T>G - r.(?) p.(Asp315Glu)
?/. - c.1051G>A VUS r.(?) p.(Gly351Arg)
-/. - c.1232A>G benign r.(?) p.(Tyr411Cys)
-/. - c.1578T>A benign r.(?) p.(=)
-?/. 5 c.1578T>A - r.(?) p.(=)
?/. 5 c.1597A>G - r.(?) p.(Thr533Ala)
?/. - c.1652A>G VUS r.(?) p.(Tyr551Cys)
?/. - c.1736A>G VUS r.(?) p.(Tyr579Cys)
-?/. - c.1988A>G likely benign r.(?) p.(Asn663Ser)
?/. - c.1997C>T VUS r.(?) p.(Ala666Val)
?/. 5 c.1997C>T - r.(?) p.(Ala666Val)
-/. - c.1997C>T benign r.(?) p.(Ala666Val)
-?/. - c.2114G>A likely benign r.(?) p.(Arg705His)
-?/. - c.2114G>A likely benign r.(?) p.(Arg705His)
?/. - c.2144G>A VUS r.(?) p.(Gly715Glu)
-?/. - c.2145A>G likely benign r.(?) p.(=)
-?/. - c.2215A>T likely benign r.(?) p.(Ile739Leu)
-?/. - c.2259G>A likely benign r.(?) p.(=)
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