Transcript #00019070 (NM_020949.2, SLC7A14 gene)

Transcript name solute carrier family 7 (orphan transporter), member 14
Gene name SLC7A14 (solute carrier family 7 (orphan transporter), member 14)
Chromosome 3
Transcript - NCBI ID NM_020949.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_066000.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.29C>G r.(?) p.(Pro10Arg)
?/. - c.98A>T r.(?) p.(Glu33Val)
?/. - c.128C>T r.(?) p.(Thr43Met)
-?/. 2 c.249A>G r.(=) p.(=)
-?/. 2 c.258T>G r.(=) p.(=)
-?/. - c.304+5G>A r.spl? p.?
?/. - c.304+5G>A r.spl? p.?
-?/. 3 c.336C>A r.(=) p.(=)
+?/. - c.395C>T r.(?) p.(Ala132Val)
?/. - c.443C>T r.(?) p.(Ala148Val)
?/. - c.489C>A r.(?) p.(Asn163Lys)
?/. - c.520G>A r.(?) p.(Val174Met)
?/. - c.541+5G>A r.spl? p.?
-?/. - c.542-7T>C r.(=) p.(=)
-?/. 4 c.582G>A r.(=) p.(=)
?/. - c.586G>A r.(?) p.(Ala196Thr)
-?/. - c.632T>C r.(?) p.(Ile211Thr)
-?/. 4 c.636C>T r.(=) p.(=)
-?/. - c.639C>A r.(?) p.(Phe213Leu)
?/. - c.691G>A r.(?) p.(Ala231Thr)
+?/. - c.710A>T r.(?) p.(Asn237Ile)
-?/. - c.714G>C r.(?) p.(Gly238=)
?/. - c.715A>C r.(?) p.(Lys239Gln)
-?/. 4 c.725C>T r.(?) p.(Ala242Val)
?/. - c.725C>T r.(?) p.(Ala242Val)
-/. - c.729G>A r.(?) p.(Glu243=)
?/. - c.748G>A r.(?) p.(Gly250Ser)
?/. - c.752G>C r.(?) p.(Trp251Ser)
?/. - c.759+5G>A r.spl? p.?
?/. - c.760-2A>G r.spl? p.?
-?/. - c.789C>T r.(?) p.(Tyr263=)
-?/. 5 c.795C>T r.(=) p.(=)
-?/. - c.821C>T r.(?) p.(Thr274Ile)
-/. - c.855C>T r.(?) p.(Ile285=)
-?/. - c.907-6T>C r.(=) p.(=)
?/. - c.953C>T r.(?) p.(Thr318Met)
?/. - c.953C>T r.(?) p.(Thr318Met)
-?/. 6 c.988G>A r.(?) p.(Gly330Arg)
?/. - c.988G>A r.(?) p.(Gly330Arg)
+/. 6 c.988G>A r.(?) p.(Gly330Arg)
+/. 6 c.988G>A r.(?) p.(Gly330Arg)
?/. - c.988G>A r.(?) p.(Gly330Arg)
+?/. 6 c.988G>A r.(?) p.(Gly330Arg)
+/. - c.988G>A r.(?) p.(Gly330Arg)
?/. - c.988G>A r.(?) p.(Gly330Arg)
+?/. - c.988G>A r.(?) p.(Gly330Arg)
+?/. - c.988G>A r.(?) p.(Gly330Arg)
+?/. 6 c.988G>A r.(?) p.(Gly330Arg)
+?/. - c.988G>A r.(?) p.(Gly330Arg)
-?/. - c.988G>A r.(?) p.(Gly330Arg)
-?/. 6 c.1074G>A r.(=) p.(=)
-/. - c.1083T>A r.(?) p.(Ile361=)
-?/. - c.1116-4C>G r.spl? p.?
-/. - c.1116-4C>G r.spl? p.?
?/. - c.1129G>A r.(?) p.(Val377Ile)
-?/. - c.1168G>C r.(?) p.(Val390Leu)
?/. - c.1168G>C r.(?) p.(Val390Leu)
?/. - c.1168G>C r.(?) p.(Val390Leu)
?/. - c.1172C>T r.(?) p.(Ser391Leu)
+?/. - c.1172C>T r.(?) p.(Ser391Leu)
+?/. - c.1172C>T r.(?) p.(Ser391Leu)
+?/. - c.1172C>T r.(?) p.(Ser391Leu)
-?/. 7 c.1173G>A r.(=) p.(=)
-/. - c.1236T>C r.(?) p.(Ser412=)
?/. - c.1244C>T r.(?) p.(Thr415Met)
-?/. 7 c.1302G>A r.(=) p.(=)
-?/. 7 c.1391G>T r.(?) p.(Cys464Phe)
?/. - c.1391G>T r.(?) p.(Cys464Phe)
-?/. - c.1391G>T r.(?) p.(Cys464Phe)
?/. - c.1391G>T r.(?) p.(Cys464Phe)
+/. 7 c.1391G>T r.(?) p.(Cys464Phe)
+?/. - c.1391G>T r.(?) p.(Cys464Phe)
+?/. 7 c.1391G>T r.(?) p.(Cys464Phe)
+?/. - c.1391G>T r.(?) p.(Cys464Phe)
-/. - c.1476T>C r.(?) p.(Asn492=)
-/. - c.1533C>T r.(?) p.(Tyr511=)
?/. - c.1574C>A r.(?) p.(Ser525Tyr)
-?/. - c.1647C>T r.(?) p.(Gly549=)
?/. - c.1667G>A r.(?) p.(Arg556Gln)
?/. - c.1682C>T r.(?) p.(Thr561Met)
?/. - c.1695G>A r.(?) p.(=)
-?/. - c.1704C>T r.(?) p.(Cys568=)
-?/. - c.1704C>T r.(?) p.(Cys568=)
?/. - c.1705G>A r.(?) p.(Val569Met)
?/. - c.1778A>G r.(?) p.(Gln593Arg)
-?/. 7 c.1890T>G r.(=) p.(=)
-?/. - c.1890T>G r.(?) p.(Pro630=)
-/. - c.1890T>G r.(?) p.(Pro630=)
+/. 7 c.1970G>A r.(?) p.(Arg657Gln)
-/. - c.1994-9G>A r.(=) p.(=)
?/. - c.2040A>C r.(?) p.(Glu680Asp)
?/. - c.2047G>A r.(?) p.(Ala683Thr)
-?/. 8 c.2083C>T r.(?) p.(Arg695Cys)
+?/. - c.2083C>T r.(?) p.(Arg695Cys)
+/. - c.2083C>T r.(?) p.(Arg695Cys)
-?/. - c.2088C>T r.(?) p.(Tyr696=)
+?/. - c.2122T>G r.(?) p.(Phe708Val)
-?/. - c.2130C>T r.(?) p.(Tyr710=)
-/. - c.2226G>A r.(?) p.(Arg742=)
-?/. - c.2226G>A r.(?) p.(Arg742=)
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