Transcript #00024014 (NM_017767.2, SLC39A4 gene)

Transcript name transcript variant 1
Gene name SLC39A4 (solute carrier family 39 (zinc transporter), member 4)
Chromosome 8
Transcript - NCBI ID NM_017767.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_060237.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2015-01-26 11:16:30 +01:00 (CET)
Date last edited N/A


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-572C>T r.(?) p.(=)
-?/. - c.-531G>A r.(?) p.(=)
?/. - c.-422C>T r.(?) p.(=)
-/. - c.-410G>A r.(?) p.(=)
?/. - c.-404G>A r.(?) p.(=)
-/. - c.-385C>A r.(?) p.(=)
?/. - c.2T>G r.(?) p.(Met1?)
-?/. - c.73T>G r.(?) p.(Ser25Ala)
-/. - c.80T>C r.(?) p.(Val27Ala)
-?/. - c.135C>T r.(?) p.(Asp45=)
-?/. - c.172C>T r.(?) p.(Pro58Ser)
-?/. - c.176C>T r.(?) p.(Pro59Leu)
?/. - c.182C>T r.(?) p.(Pro61Leu)
-?/. - c.182C>T r.(?) p.(Pro61Leu)
-?/. - c.182C>T r.(?) p.(Pro61Leu)
-?/. - c.183G>A r.(?) p.(Pro61=)
-?/. - c.204C>T r.(?) p.(Val68=)
-?/. - c.246C>T r.(?) p.(Pro82=)
-?/. - c.249G>A r.(?) p.(Glu83=)
-?/. - c.264C>T r.(?) p.(Asp88=)
-?/. - c.265G>A r.(?) p.(Ala89Thr)
-?/. - c.338C>T r.(?) p.(Pro113Leu)
-?/. - c.389C>T r.(?) p.(Thr130Ile)
-?/. - c.405C>T r.(?) p.(Cys135=)
-?/. - c.429G>A r.(?) p.(Glu143=)
-?/. - c.429G>A r.(?) p.(Glu143=)
?/. - c.457A>T r.(?) p.(Ser153Cys)
-?/. - c.465C>T r.(?) p.(Gly155=)
-?/. - c.520T>C r.(?) p.(Leu174=)
-?/. - c.520T>C r.(?) p.(Leu174=)
+/. - c.524C>T r.(?) p.(Pro175Leu)
-?/. - c.585G>A r.(?) p.(Thr195=)
?/. - c.613C>T r.(?) p.(Arg205Cys)
-?/. - c.648C>T r.(?) p.(His216=)
?/. - c.655C>T r.(?) p.(Arg219Trp)
-/. - c.676= r.(=) p.(Arg226=)
-/. - c.676= r.(=) p.(Arg226=)
-?/. - c.729+9C>T r.(=) p.(=)
-?/. - c.729+10G>A r.(=) p.(=)
-?/. - c.730-12G>T r.(=) p.(=)
-?/. - c.765T>C r.(?) p.(Tyr255=)
?/. - c.773C>T r.(?) p.(Ser258Leu)
-?/. - c.774G>A r.(?) p.(Ser258=)
?/. - c.794C>T r.(?) p.(Pro265Leu)
-?/. - c.901+16G>A r.(=) p.(=)
-?/. - c.927G>A r.(?) p.(Thr309=)
-?/. - c.928C>T r.(?) p.(Leu310=)
-?/. - c.945C>T r.(?) p.(Cys315=)
?/. - c.947C>T r.(?) p.(Ala316Val)
?/. - c.947C>T r.(?) p.(Ala316Val)
-?/. - c.979G>A r.(?) p.(Gly327Ser)
-/. - c.994A>G r.(?) p.(Thr332Ala)
-/. - c.994A>G r.(?) p.(Thr332Ala)
?/. - c.1039C>G r.(?) p.(Leu347Val)
+?/. - c.1045G>A r.(?) p.(Gly349Arg)
?/. - c.1051G>A r.(?) p.(Ala351Thr)
-/. - c.1066A>G r.(?) p.(Thr356Ala)
-?/. - c.1074+8C>T r.(=) p.(=)
-?/. - c.1075-15G>A r.(=) p.(=)
-?/. - c.1130G>A r.(?) p.(Arg377His)
-?/. - c.1234G>A r.(?) p.(Gly412Ser)
?/. - c.1296C>T r.(?) p.(Ser432=)
-?/. - c.1321C>A r.(?) p.(His441Asn)
-?/. - c.1341C>T r.(?) p.(Asp447=)
-?/. - c.1351G>A r.(?) p.(Glu451Lys)
-?/. - c.1363G>A r.(?) p.(Glu455Lys)
-?/. - c.1399+19C>T r.(=) p.(=)
?/. - c.1400-5C>A r.spl? p.?
-?/. - c.1420A>G r.(?) p.(Met474Val)
-?/. - c.1420A>G r.(?) p.(Met474Val)
?/. - c.1433G>T r.(?) p.(Gly478Val)
?/. - c.1434C>T r.(?) p.(Gly478=)
?/. - c.1514C>T r.(?) p.(Ser505Leu)
-?/. - c.1584G>C r.(?) p.(Leu528=)
-?/. - c.1584G>C r.(?) p.(Leu528=)
-?/. - c.1629G>A r.(?) p.(Thr543=)
?/. - c.1629G>A r.(?) p.(Thr543=)
-?/. - c.1668C>T r.(?) p.(Val556=)
-?/. - c.1668C>T r.(?) p.(Val556=)
?/. - c.1702G>A r.(?) p.(Ala568Thr)
-?/. - c.*3430C>A r.(=) p.(=)
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