Transcript #00019275 (NM_080877.2, SLC34A3 gene)

Transcript name transcript variant 3
Gene name SLC34A3 (solute carrier family 34 (sodium phosphate), member 3)
Chromosome 9
Transcript - NCBI ID NM_080877.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_543153.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

88 entries on 1 page. Showing entries 1 - 88.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-5181C>T r.(?) p.(=)
?/. - c.-2272C>T r.(?) p.(=)
-?/. - c.-39-6C>T r.(=) p.(=)
-/. - c.86-120C>T r.(=) p.(=)
-/. - c.200G>A r.(?) p.(Arg67His)
-?/. - c.211G>A r.(?) p.(Gly71Ser)
+/. - c.231C>A r.(?) p.(Cys77*)
-/. - c.273C>T r.(?) p.(Asp91=)
-?/. - c.274G>A r.(?) p.(Val92Ile)
?/. - c.286G>A r.(?) p.(Ala96Thr)
+/. - c.304+2T>C r.spl? p.?
-?/. - c.305-5T>C r.spl? p.?
-?/. - c.306C>T r.(?) p.(Ser102=)
-?/. - c.310G>C r.(?) p.(Val104Leu)
?/. - c.371T>C r.(?) p.(Ile124Thr)
-?/. - c.396G>A r.(?) p.(Val132=)
-?/. - c.399G>A r.(?) p.(=)
-?/. - c.539G>C r.(?) p.(Gly180Ala)
+?/. - c.560+27_561-38del r.(?) p.(=)
+/. - c.575C>T r.(?) p.(Ser192Leu)
+/. - c.575C>T r.(?) p.(Ser192Leu)
+/. - c.575C>T r.(?) p.(Ser192Leu)
-/. - c.625C>T r.(?) p.(Leu209=)
-?/. - c.679G>A r.(?) p.(Ala227Thr)
-?/. - c.709G>A r.(?) p.(Asp237Asn)
?/. - c.709G>A r.(?) p.(Asp237Asn)
-?/. - c.709G>A r.(?) p.(Asp237Asn)
?/. - c.709G>A r.(?) p.(Asp237Asn)
?/. - c.740C>G r.(?) p.(Thr247Arg)
-?/. - c.756G>A r.(?) p.(Gln252=)
-?/. - c.756G>A r.(?) p.(Gln252=)
?/. - c.756G>A r.(?) p.(Gln252=)
-/. - c.756+9G>A r.(=) p.(=)
-/. - c.757T>C r.(?) p.(Leu253=)
-/. - c.757T>C r.(?) p.(Leu253=)
-/. - c.757T>C r.(?) p.(Leu253=)
-?/. - c.757T>C r.(?) p.(Leu253=)
-?/. - c.779G>A r.(?) p.(Ser260Asn)
-?/. - c.779G>A r.(?) p.(Ser260Asn)
-?/. - c.790G>A r.(?) p.(Gly264Ser)
-/. - c.790G>A r.(?) p.(Gly264Ser)
?/. - c.795C>T r.(?) p.(=)
-?/. - c.836C>T r.(?) p.(Thr279Met)
-?/. - c.919C>A r.(?) p.(Leu307Met)
+/. - c.925+20_926-48del r.(?) p.(=)
-?/. - c.929G>A r.(?) p.(Arg310His)
-?/. - c.929G>A r.(?) p.(Arg310His)
+/. - c.944del r.(?) p.(Gly315AlafsTer28)
?/. - c.949_967dup r.(?) p.(Val323Glyfs*276)
?/. - c.953T>C r.(?) p.(Leu318Pro)
-?/. - c.1009G>A r.(?) p.(Gly337Ser)
+?/. - c.1053_1060del r.(?) p.(Arg353Profs*237)
-?/. - c.1074G>A r.(?) p.(=)
-?/. - c.1093+9G>A r.(=) p.(=)
?/. - c.1094-4A>C r.spl? p.?
-?/. - c.1140C>T r.(?) p.(Leu380=)
?/. - c.1143G>A r.(?) p.(=)
-/. - c.1149C>T r.(?) p.(=)
-?/. - c.1164A>G r.(?) p.(Ala388=)
-?/. - c.1170G>A r.(?) p.(Gln390=)
-?/. - c.1191G>A r.(?) p.(Ala397=)
-?/. - c.1197C>G r.(?) p.(Val399=)
+?/. - c.1267G>T r.(?) p.(Gly423Cys)
-?/. - c.1309G>A r.(?) p.(Ala437Thr)
+/. 12i c.1335+2T>A r.spl p.?
+/. 12i c.1335+2T>A r.spl p.?
?/. - c.1453C>T r.(?) p.(Arg485Cys)
+?/. - c.1453C>T r.(?) p.(Arg485Cys)
?/. - c.1453C>T r.(?) p.(Arg485Cys)
-/. - c.1454G>A r.(?) p.(Arg485His)
-?/. - c.1454G>A r.(?) p.(Arg485His)
-?/. - c.1454G>A r.(?) p.(Arg485His)
?/. - c.1454G>A r.(?) p.(Arg485His)
-?/. - c.1512C>T r.(?) p.(Phe504=)
-?/. - c.1512C>T r.(?) p.(Phe504=)
-/. - c.1512C>T r.(?) p.(Phe504=)
-/. - c.1538= r.(=) p.(Val513=)
-?/. - c.1538= r.(?) p.(Val513=)
-/. - c.1538= r.(=) p.(Val513=)
-?/. - c.1585A>T r.(?) p.(Ile529Phe)
-?/. - c.1585A>T r.(?) p.(Ile529Phe)
-?/. - c.1612C>T r.(?) p.(Arg538Trp)
-?/. - c.1633C>T r.(?) p.(Arg545Cys)
+/. 13 c.1639_1652del r.(?) p.(Arg547Alafs*41)
+/. 13 c.1639_1652del r.(?) p.(Arg547Alafs*41)
?/. - c.1690C>A r.(?) p.(Arg564Ser)
-/. - c.*14A>C r.(=) p.(=)
-/. - c.*14A>C r.(=) p.(=)
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