Transcript #00019273 (NM_003052.4, SLC34A1 gene)

Transcript name transcript variant 1
Gene name SLC34A1 (solute carrier family 34 (sodium phosphate), member 1)
Chromosome 5
Transcript - NCBI ID NM_003052.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_003043.3
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

86 entries on 1 page. Showing entries 1 - 86.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.56G>A r.(?) p.(Arg19His)
+/. - c.73C>T r.(?) p.(Arg25*)
?/. - c.80C>T r.(?) p.(Thr27Met)
+?/. - c.272_292del r.(?) p.(Val91_Ala97del)
+?/. 4 c.272_292del r.(?) p.(Val91_Ala97del)
+?/. 4 c.272_292del r.(?) p.(Val91_Ala97del)
+?/. 4 c.272_292del r.(?) p.(Val91_Ala97del)
+?/. 4 c.272_292del r.(?) p.(Val91_Ala97del)
+?/. 4 c.272_292del r.(?) p.(Val91_Ala97del)
+?/. 4 c.272_292del r.(?) p.Val91_Ala97del
-?/. - c.272_292del r.(?) p.(Val91_Ala97del)
-/. - c.272_292del r.(?) p.(Val91_Ala97del)
-/. - c.272_292del r.(?) p.(Val91_Ala97del)
-?/. - c.284G>A r.(?) p.(Arg95His)
-/. - c.389-20C>T r.(=) p.(=)
-/. - c.389-20C>T r.(=) p.(=)
?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.398C>T r.(?) p.(Ala133Val)
?/. - c.398C>T r.(?) p.(Ala133Val)
?/. - c.437C>T r.(?) p.(Pro146Leu)
?/. - c.437C>T r.(?) p.(Pro146Leu)
?/. - c.449T>A r.(?) p.(Leu150Gln)
+/. 5 c.458G>C r.(?) p.(Gly153Ala)
+/. 5 c.458G>C r.(?) p.(Gly153Ala)
+/. 5 c.458G>C r.(?) p.(Gly153Ala)
+/. 5 c.458G>C r.(?) p.Gly153Ala
+/. 5 c.458G>T r.(?) p.(Gly153Val)
+/. 5 c.458G>T r.(?) p.Gly153Val
+/. - c.458G>T r.(?) p.(Gly153Val)
+/. 5 c.458G>T r.(?) p.(Gly153Val)
+/. 5 c.464T>C r.(?) p.(Leu155Pro)
+/. 5 c.464T>C r.(?) p.Leu155Pro
+?/. - c.464T>C r.(?) p.(Leu155Pro)
+/. 6 c.557_558del r.(?) p.(Pro186Hisfs*26)
?/. - c.592A>C r.(?) p.(Thr198Pro)
?/. - c.604G>A r.(?) p.(Val202Met)
?/. - c.632C>A r.(?) p.(Thr211Asn)
+/. 6 c.644G>A r.spl? p.(Arg215Gln)
+/. 6i c.644+1G>A r.spl p.?
+/. 6i c.644+1G>A r.spl p.?
?/. - c.662C>T r.(?) p.(Thr221Met)
-?/. - c.741C>A r.(?) p.(=)
-/. - c.774T>C r.(?) p.(His258=)
-/. - c.774T>C r.(?) p.(His258=)
+?/. - c.782_810del r.(?) p.(Arg261HisfsTer23)
+/. 8 c.914G>A r.(?) p.(Trp305*)
+?/. - c.937-8T>A r.(?) p.(?)
+/. 9 c.1006T>G r.(?) p.(Cys336Gly)
+/. 9 c.1006T>G r.(?) p.Cys336Gly
+/. - c.1006+1G>A r.spl? p.?
+/. - c.1006+1G>A r.spl? p.?
+/. 9i c.1006+1G>A r.spl p.?
+?/. - c.1006+1G>A r.spl p.?
+/. 9i c.1006+3_1006+6del r.spl p.?
?/. - c.1007-13_1007-5del r.spl? p.?
?/. 10 c.1016T>C r.(?) p.(Ile339Thr)
?/. - c.1037C>T r.(?) p.(Pro346Leu)
+/. 11 c.1223T>A r.(?) p.(Val408Glu)
+/. 11 c.1223T>A r.(?) p.(Val408Glu)
+/. 11 c.1223T>A r.(?) p.Val408Glu
+?/. - c.1325C>T r.(?) p.(Pro442Leu)
-?/. - c.1416+3G>A r.spl? p.?
+/. 12i c.1416+5G>A r.spl p.?
+/. 12i c.1416+5G>A r.spl p.?
+/. 13 c.1425_1426del r.(?) p.(Cys476Serfs*128)
+/. 13 c.1425_1426del r.(?) p.Cys476Serfs*128
+/. 13 c.1462T>C r.(?) p.(Trp488Arg)
+/. 13 c.1462T>C r.(?) p.Trp488Arg
?/. - c.1497C>T r.(?) p.(Arg499=)
+/. 13 c.1614G>A r.(?) p.(Trp538*)
-/. - c.1702C>T r.(?) p.(His568Tyr)
-/. - c.1702C>T r.(?) p.(His568Tyr)
-?/. - c.1702C>T r.(?) p.(His568Tyr)
+/. - c.*4174C>T r.(=) p.(=)
-?/. - c.*4180C>T r.(=) p.(=)
-?/. - c.*5126G>C r.(=) p.(=)
-?/. - c.*5164C>T r.(=) p.(=)
-?/. - c.*5283G>A r.(=) p.(=)
-?/. - c.*5301G>A r.(=) p.(=)
+/. - c.*5332C>T r.(=) p.(=)
-/. - c.*5340G>A r.(=) p.(=)
-/. - c.*5340G>A r.(=) p.(=)
-?/. - c.*5340G>C r.(=) p.(=)
-?/. - c.*5340G>C r.(=) p.(=)
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