Transcript #00017338 (NM_025243.3, SLC19A3 gene)

Transcript name solute carrier family 19, member 3
Gene name SLC19A3 (solute carrier family 19, member 3)
Chromosome 2
Transcript - NCBI ID NM_025243.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_079519.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

87 entries on 1 page. Showing entries 1 - 87.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-2-49T>C r.(=) p.(=)
?/? c.-2-40T>C r.(=) p.(=)
?/? c.-2-10A>G r.(=) p.(=)
?/? c.16A>G r.(?) p.(Thr6Ala)
?/? c.18T>A r.(=) p.(=)
?/? c.24A>T r.(=) p.(=)
?/? c.42C>T r.(=) p.(=)
?/? c.56T>C r.(?) p.(Leu19Pro)
?/? c.103C>T r.(?) p.(Leu35Phe)
?/? c.106A>G r.(?) p.(Ile36Val)
?/? c.112T>C r.(?) p.(Tyr38His)
?/? c.141C>A r.(=) p.(=)
?/? c.150+21A>G r.(=) p.(=)
?/? c.150+32G>A r.(=) p.(=)
?/? c.151-36G>T r.(=) p.(=)
?/? c.151-25G>A r.(=) p.(=)
?/? c.187T>C r.(?) p.(Tyr63His)
?/? c.217C>T r.(?) p.(Leu73Phe)
?/? c.260G>A r.(?) p.(Gly87Asp)
?/? c.309G>A r.(=) p.(=)
?/? c.337T>C r.(?) p.(Tyr113His)
?/? c.355G>A r.(?) p.(Ala119Thr)
?/? c.387C>T r.(=) p.(=)
?/? c.390G>T r.(=) p.(=)
?/? c.399C>G r.(=) p.(=)
?/? c.412A>G r.(?) p.(Arg138Gly)
?/? c.421G>A r.(?) p.(Gly141Ser)
?/? c.435C>T r.(=) p.(=)
?/? c.436G>A r.(?) p.(Val146Ile)
?/? c.465G>A r.(=) p.(=)
?/? c.481T>C r.(=) p.(=)
?/? c.494C>A r.(?) p.(Ala165Glu)
?/? c.500T>A r.(?) p.(Met167Lys)
?/? c.503C>G r.(?) p.(Ser168Trp)
?/? c.520G>A r.(?) p.(Val174Ile)
?/? c.546G>A r.(=) p.(=)
?/? c.549T>C r.(=) p.(=)
?/? c.557T>C r.(?) p.(Phe186Ser)
?/? c.562C>G r.(?) p.(Leu188Val)
?/? c.567C>T r.(=) p.(=)
?/? c.592T>C r.(?) p.(Phe198Leu)
?/? c.613A>G r.(?) p.(Arg205Gly)
?/? c.621A>G r.(?) p.(Ile207Met)
?/? c.636C>T r.(=) p.(=)
?/? c.663C>T r.(=) p.(=)
?/? c.680G>A r.(?) p.(Gly227Asp)
?/? c.738G>C r.(?) p.(Lys246Asn)
?/? c.745C>T r.(=) p.(=)
?/? c.751A>G r.(?) p.(Ser251Gly)
?/? c.756G>A r.(=) p.(=)
?/? c.801A>G r.(=) p.(=)
?/? c.854G>A r.(?) p.(Trp285*)
?/? c.870A>G r.(=) p.(=)
?/? c.893A>G r.(?) p.(Tyr298Cys)
?/? c.919G>C r.(?) p.(Ala307Pro)
?/? c.947A>G r.(?) p.(Asn316Ser)
?/? c.955G>A r.(?) p.(Val319Ile)
?/? c.979+19A>G r.(=) p.(=)
?/? c.979+29G>T r.(=) p.(=)
?/? c.979+42G>C r.(=) p.(=)
?/? c.979+42_979+43insG r.(=) p.(=)
?/? c.979+52A>G r.(=) p.(=)
?/? c.980-38_980-37insA r.(=) p.(=)
?/? c.980-4del r.spl? p.?
?/? c.987G>A r.(=) p.(=)
?/? c.1049T>C r.(?) p.(Val350Ala)
?/? c.1056C>G r.(?) p.(Phe352Leu)
?/? c.1112C>T r.(?) p.(Ala371Val)
?/? c.1132A>G r.(?) p.(Ile378Val)
?/? c.1145G>A r.(?) p.(Ser382Asn)
?/? c.1166T>C r.(?) p.(Ile389Thr)
?/? c.1172+5G>A r.spl? p.?
?/? c.1173-47C>T r.(=) p.(=)
?/? c.1173-4A>T r.spl? p.?
?/? c.1186G>T r.(?) p.(Val396Phe)
?/? c.1204C>T r.(?) p.(Arg402Cys)
?/? c.1314+1G>A r.spl? p.?
?/? c.1315-23G>A r.(=) p.(=)
?/? c.1354del r.(?) p.(Ile452Phefs*3)
?/? c.1355T>C r.(?) p.(Ile452Thr)
?/? c.1370G>A r.(?) p.(Ser457Asn)
?/? c.1381_1382insTTA r.(?) p.(Ile460dup)
?/? c.1397C>T r.(?) p.(Ser466Phe)
?/? c.1441G>A r.(?) p.(Val481Met)
?/? c.*5A>G r.(=) p.(=)
?/? c.*8G>T r.(=) p.(=)
?/? c.*25G>A r.(=) p.(=)
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