Transcript #00019052 (NM_001003841.2, SLC6A19 gene)

Transcript name solute carrier family 6 (neutral amino acid transporter), member 19
Gene name SLC6A19 (solute carrier family 6 (neutral amino acid transporter), member 19)
Chromosome 5
Transcript - NCBI ID NM_001003841.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001003841.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

95 entries on 1 page. Showing entries 1 - 95.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-14G>A r.(?) p.(=)
-/. - c.-8C>T r.(?) p.(=)
?/. - c.4G>T r.(?) p.(Val2Leu)
-?/. - c.72C>T r.(?) p.(Ile24=)
?/. - c.73G>C r.(?) p.(Glu25Gln)
?/. - c.97C>A r.(?) p.(Pro33Thr)
-/. - c.114G>A r.(?) p.(Lys38=)
-?/. - c.117G>A r.(?) p.(Ala39=)
+?/. - c.118_119del r.(?) p.(Gln40Valfs*312)
-?/. - c.156C>T r.(?) p.(Leu52=)
-?/. - c.156C>T r.(?) p.(Leu52=)
-?/. - c.162C>T r.(?) p.(Asn54=)
-?/. - c.195C>T r.(?) p.(His65=)
-?/. - c.195C>T r.(?) p.(His65=)
-/. - c.306T>C r.(?) p.(Gly102=)
-/. - c.306T>C r.(?) p.(Gly102=)
-/. - c.306T>C r.(?) p.(Gly102=)
-?/. - c.306T>G r.(?) p.(Gly102=)
+?/. 2 c.307G>A r.(?) p.(Val103Met)
?/. - c.314G>A r.(?) p.(Ser105Asn)
?/. - c.326C>A r.(?) p.(Pro109Gln)
?/. - c.326C>A r.(?) p.(Pro109Gln)
-?/. - c.343+37_343+75del r.(=) p.(=)
+/. - c.374_377del r.(?) p.(Val125AspfsTer109)
-?/. - c.453C>T r.(?) p.(Ser151=)
?/. - c.484T>C r.(?) p.(Tyr162His)
+/. - c.517G>A r.(?) p.(Asp173Asn)
+/. - c.517G>A r.(?) p.(Asp173Asn)
+/. - c.517G>A r.(?) p.(Asp173Asn)
+?/. - c.517G>A r.(?) p.(Asp173Asn)
+/. - c.517G>A r.(?) p.(Asp173Asn)
+/. - c.517G>A r.(?) p.(Asp173Asn)
?/. - c.539C>T r.(?) p.(Thr180Met)
?/. - c.547A>C r.(?) p.(Ile183Leu)
-?/. - c.555G>A r.(?) p.(Thr185=)
-?/. - c.555G>A r.(?) p.(Thr185=)
-/. - c.558C>T r.(?) p.(Ser186=)
-?/. - c.579C>A r.(?) p.(Ile193=)
-?/. - c.642C>T r.(?) p.(Arg214=)
-/. - c.663+16G>A r.(=) p.(=)
-/. - c.663+16G>A r.(=) p.(=)
?/. - c.697G>A r.(?) p.(Val233Ile)
+?/. 5 c.697G>A r.(?) p.(Val233Ile)
?/. - c.727A>G r.(?) p.(Thr243Ala)
?/. - c.727A>G r.(?) p.(Thr243Ala)
-/. - c.754G>A r.(?) p.(Val252Ile)
-?/. - c.768G>A r.(?) p.(Thr256=)
+?/. - c.774+1G>A r.spl? p.?
+?/. - c.774+1G>A r.spl? p.?
-?/. - c.775-5C>T r.spl? p.?
-?/. - c.775-5C>T r.spl? p.?
-?/. - c.775-5C>T r.spl? p.?
-?/. - c.775-4G>A r.spl? p.?
?/. - c.779C>T r.(?) p.(Thr260Met)
-?/. - c.813G>A r.(?) p.(Ala271=)
-?/. - c.849C>T r.(?) p.(Phe283=)
-/. - c.888-3C>T r.spl? p.?
-/. - c.966C>T r.(?) p.(Tyr322=)
?/. - c.983G>A r.(?) p.(Arg328His)
-?/. - c.984C>T r.(?) p.(Arg328=)
-?/. - c.984C>T r.(?) p.(Arg328=)
-?/. - c.984C>T r.(?) p.(Arg328=)
-/. - c.990A>G r.(?) p.(Thr330=)
-/. - c.990A>G r.(?) p.(Thr330=)
-/. - c.990A>G r.(?) p.(Thr330=)
?/. - c.995G>A r.(?) p.(Arg332His)
-/. - c.1002C>T r.(?) p.(Asp334=)
-/. - c.1017-4G>A r.spl? p.?
-/. - c.1017-4G>A r.spl? p.?
-/. - c.1017-4G>A r.spl? p.?
-?/. - c.1044C>T r.(?) p.(Phe348=)
-?/. - c.1044C>T r.(?) p.(Phe348=)
?/. - c.1063G>A r.(?) p.(Val355Met)
-?/. - c.1107C>G r.(?) p.(Ala369=)
-?/. - c.1119G>A r.(?) p.(Ala373=)
-?/. - c.1125C>T r.(?) p.(Tyr375=)
+/. - c.1173+2T>G r.spl p.?
+/. - c.1173+2T>G r.spl? p.?
+/. - c.1173+2T>G r.spl? p.?
+/. - c.1173+2T>G r.spl? p.?
-/. - c.1173+14G>A r.(=) p.(=)
?/. - c.1244T>C r.(?) p.(Leu415Pro)
?/. - c.1244T>C r.(?) p.(Leu415Pro)
?/. - c.1373T>C r.(?) p.(Leu458Pro)
-/. - c.1379-9G>C r.(=) p.(=)
-?/. - c.1422G>A r.(?) p.(Thr474=)
?/. - c.1469G>A r.(?) p.(Gly490Asp)
?/. - c.1492G>A r.(?) p.(Ala498Thr)
+?/. - c.1556A>G r.(?) p.(Glu519Gly)
?/. - c.1606G>A r.(?) p.(Val536Met)
?/. - c.1648_1650del r.(?) p.(Phe550del)
-/. - c.1701C>T r.(?) p.(Tyr567=)
-?/. - c.1704G>A r.(?) p.(Glu568=)
-?/. - c.1825C>G r.(?) p.(His609Asp)
-?/. - c.1891G>A r.(?) p.(Asp631Asn)
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