Transcript #00019178 (NM_004727.2, SLC24A1 gene)

Transcript name transcript variant 1
Gene name SLC24A1 (solute carrier family 24 (sodium/potassium/calcium exchanger), member 1)
Chromosome 15
Transcript - NCBI ID NM_004727.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_004718.1
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

124 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. 2 c.87G>A r.spl p.(Leu29=)
+/. - c.95T>A r.(?) p.(Leu32*)
-/. - c.109A>T r.(?) p.(Thr37Ser)
-/. 2 c.109A>T r.(?) p.(Thr37Ser)
-?/. - c.120C>T r.(?) p.(His40=)
-?/. - c.120C>T r.(?) p.(His40=)
+/. - c.172C>T r.(?) p.(Gln58Ter)
-?/. - c.192T>C r.(?) p.(Ser64=)
-?/. - c.253G>A r.(?) p.(Glu85Lys)
-?/. - c.531C>T r.(?) p.(Tyr177=)
-?/. - c.601G>A r.(?) p.(Val201Met)
+/. - c.680del r.(?) p.(Ala227Glufs*14)
-/. 2 c.716G>C r.(?) p.(Arg239Thr)
+/. - c.754_755del r.(?) p.(Met252Valfs*2)
+?/. - c.754_755del r.(?) p.(Met252Valfs*2)
+?/. 2 c.754_755del r.(?) p.(Met252Valfs*2)
?/. - c.772A>G r.(?) p.(Thr258Ala)
-?/. - c.802G>A r.(?) p.(Val268Ile)
?/. - c.803T>C r.(?) p.(Val268Ala)
-?/. - c.931G>C r.(?) p.(Val311Leu)
-?/. 2 c.931G>C r.(?) p.(Val311Leu)
-/. 2 c.937T>G r.(?) p.(Leu313Val)
-/. - c.939G>A r.(?) p.(Leu313=)
-/. 2 c.991A>T r.(?) p.(Ser331Cys)
-?/. - c.1131C>T r.(?) p.(Thr377=)
?/. - c.1136C>T r.(?) p.(Thr379Ile)
-?/. - c.1166T>A r.(?) p.(Met389Lys)
-?/. 2 c.1166T>A r.(?) p.(Met389Lys)
-?/. - c.1242C>G r.(?) p.(Ala414=)
-/. - c.1242C>G r.(?) p.(Ala414=)
+/. - c.1320C>G r.(?) p.(Tyr440Ter)
?/. - c.1375G>A r.(?) p.(Val459Ile)
?/. 2 c.1375G>A r.(?) p.(Val459Ile)
?/. - c.1450A>T r.(?) p.(Ile484Phe)
?/. - c.1454C>T r.(?) p.(Thr485Ile)
?/. - c.1454C>T r.(?) p.(Thr485Ile)
-/. - c.1454C>T r.(?) p.(Thr485Ile)
-/. - c.1488C>T r.(?) p.(Gly496=)
-/. - c.1488C>T r.(?) p.(Gly496=)
+?/. - c.1613_1614del r.(?) p.(Phe538Cysfs*23)
+?/. - c.1613_1614del r.(?) p.(Phe538Cysfs*23)
+?/. - c.1613_1614del r.(?) p.(Phe538Cysfs*23)
+?/. - c.1613_1614del r.(?) p.(Phe538Cysfs*23)
+?/. - c.1613_1614del r.(?) p.(Phe538Cysfs*23)
+/. 2 c.1613_1614del r.(?) p.(Phe538Cysfs*23)
-?/. 2 c.1653C>T r.(?) p.(Leu551=)
+/. 2 c.1691_1693del r.(?) p.(Phe564del)
+?/. 2 c.1715T>C r.(?) p.(Leu572Pro)
?/. - c.1771_1773del r.(?) p.(Leu591del)
-?/. 2 c.1822G>A r.(?) p.(Val608Ile)
-?/. - c.1859C>T r.(?) p.(Ala620Val)
-?/. - c.1859C>T r.(?) p.(Ala620Val)
-?/. 2i c.1891-6T>C r.spl? p.?
-?/. - c.1892C>T r.(?) p.(Pro631Leu)
-?/. - c.1893G>A r.(?) p.(Pro631=)
-?/. - c.1925A>G r.(?) p.(Gln642Arg)
-?/. 3i c.1945-58G>A r.(?) p.?
-?/. 3i c.1945-22_1945-21insAGGACTG r.(?) p.?
-/. - c.1945-22_1945-21insAGGCCTG r.(=) p.(=)
+?/. Ex4 c.1963C>T r.(?) p.(Arg655*)
?/. - c.1976C>T r.(?) p.(Ser659Leu)
+/. - c.2002C>T r.(?) p.(Arg668Cys)
?/. - c.2002C>T r.(?) p.(Arg668Cys)
-?/. - c.2054-1450C>T r.(=) p.(=)
-?/. - c.2054-1423C>G r.(=) p.(=)
-/. - c.2054-1401C>T r.(=) p.(=)
?/. - c.2054-6T>C r.(=) p.(=)
-?/. 4i c.2054-6T>C r.spl? p.?
?/. - c.2071_2073del r.(?) p.(Lys691del)
?/. - c.2171C>T r.(?) p.(Thr724Met)
?/. - c.2183C>T r.(?) p.(Ala728Val)
?/. - c.2183C>T r.(?) p.(Ala728Val)
+?/. 6 c.2186del r.(?) p.(Pro729Leufs*93)
-?/. 7 c.2326G>C r.(?) p.(Glu776Gln)
-?/. - c.2349T>C r.(?) p.(Gly783=)
+/. 7 c.2401G>T r.(?) p.(Glu801*)
+/. 7 c.2401G>T r.(?) p.(Glu801*)
-?/. - c.2445C>T r.(?) p.(His815=)
-?/. - c.2445C>T r.(?) p.(His815=)
?/. - c.2452G>A r.(?) p.(Asp818Asn)
?/. - c.2589_2597del r.(?) p.(Glu866_Glu868del)
-/. - c.2594A>G r.(?) p.(Glu865Gly)
-/. - c.2594A>G r.(?) p.(Glu865Gly)
-?/. - c.2628_2654del r.(?) p.(Gln878_Glu886del)
-/. 7 c.2628_2654del r.(?) p.(Gln878_Glu886del)
?/. - c.2632_2643dup r.(?) p.(Gln878_Glu881dup)
?/. - c.2658_2660del r.(?) p.(Glu890del)
-/. - c.2658_2660del r.(?) p.(Glu890del)
-/. 7 c.2658_2660dup r.(?) p.(Glu890dup)
+/. - c.2679del r.(?) p.(Asn893Lysfs*31)
-?/. 7 c.2749A>G r.(?) p.(Ile917Val)
?/. - c.2764T>C r.(?) p.(Trp922Arg)
-?/. - c.2764T>C r.(?) p.(Trp922Arg)
-?/. 7 c.2764T>C r.(?) p.(Trp922Arg)
-?/. - c.2778C>T r.(?) p.(Pro926=)
-/. - c.2778C>T r.(?) p.(Pro926=)
-?/. 7 c.2778C>T r.(?) p.(Pro926=)
-?/. - c.2797T>G r.(?) p.(Ser933Ala)
?/. - c.2813T>G r.(?) p.(Val938Gly)
+/. - c.2817del r.(?) p.(Phe939Leufs*10)
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