Transcript #00019332

Transcript name transcript variant 2
Gene name SLC39A13 (solute carrier family 39 (zinc transporter), member 13)
Chromosome 11
Transcript - NCBI ID NM_152264.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_689477.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

18 entries on 1 page. Showing entries 1 - 18.
Legend  

Affects function     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
-/. - c.58A>G benign r.(?) p.(Thr20Ala)
-/. - c.83A>G benign r.(?) p.(Glu28Gly)
-/. - c.83A>G benign r.(?) p.(Glu28Gly)
-/. - c.119G>A benign r.(?) p.(Arg40Gln)
-?/. - c.216C>T likely benign r.(?) p.(=)
-/. - c.301+15G>A benign r.(=) p.(=)
-/. - c.301+20C>T benign r.(=) p.(=)
-?/. - c.398C>T likely benign r.(?) p.(Thr133Met)
-?/. - c.415+17G>A likely benign r.(=) p.(=)
-/. - c.416-13C>T benign r.(=) p.(=)
-?/. - c.439C>G likely benign r.(?) p.(Gln147Glu)
-?/. - c.571G>A likely benign r.(?) p.(Ala191Thr)
-/. - c.573G>A benign r.(?) p.(=)
-?/. - c.696C>T likely benign r.(?) p.(=)
-?/. - c.738C>T likely benign r.(?) p.(=)
-?/. - c.919+7G>A likely benign r.(=) p.(=)
-?/. - c.919+16G>A likely benign r.(=) p.(=)
-?/. - c.1016C>T likely benign r.(?) p.(Pro339Leu)
Legend