ClinVar Miner

List of variants in gene SLC44A1 reported as uncertain significance for not specified

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_080546.5(SLC44A1):c.1256A>T (p.Asp419Val) rs139138357 0.00026
NM_080546.5(SLC44A1):c.1082C>G (p.Thr361Ser) rs138697456 0.00016
NM_080546.5(SLC44A1):c.1306A>G (p.Ile436Val) rs149543662 0.00015
NM_080546.5(SLC44A1):c.1924G>A (p.Ala642Thr) rs368075040 0.00005
NM_080546.5(SLC44A1):c.859C>T (p.Arg287Trp) rs141353650 0.00005
NM_080546.5(SLC44A1):c.937C>T (p.Arg313Cys) rs145083133 0.00005
NM_080546.5(SLC44A1):c.1363A>C (p.Ile455Leu) rs200282835 0.00004
NM_080546.5(SLC44A1):c.1223C>T (p.Ala408Val) rs908990838 0.00003
NM_080546.5(SLC44A1):c.1805C>G (p.Ala602Gly) rs113758350 0.00003
NM_080546.5(SLC44A1):c.23C>T (p.Ser8Phe) rs995646875 0.00003
NM_080546.5(SLC44A1):c.1499C>T (p.Ala500Val) rs750319700 0.00002
NM_080546.5(SLC44A1):c.1720A>G (p.Ile574Val) rs925021038 0.00002
NM_080546.5(SLC44A1):c.368A>G (p.Lys123Arg) rs144367903 0.00002
NM_080546.5(SLC44A1):c.1289C>T (p.Ala430Val) rs149528583 0.00001
NM_080546.5(SLC44A1):c.137G>A (p.Cys46Tyr) rs879762786 0.00001
NM_080546.5(SLC44A1):c.163G>A (p.Ala55Thr) rs552294344 0.00001
NM_080546.5(SLC44A1):c.1786G>T (p.Val596Leu) rs1334956392 0.00001
NM_080546.5(SLC44A1):c.397G>A (p.Glu133Lys) rs763560042 0.00001
NM_080546.5(SLC44A1):c.709T>A (p.Ser237Thr) rs945705326 0.00001
NM_080546.5(SLC44A1):c.1025T>C (p.Phe342Ser)
NM_080546.5(SLC44A1):c.1093C>T (p.Pro365Ser)
NM_080546.5(SLC44A1):c.1166T>A (p.Val389Glu) rs1322251431
NM_080546.5(SLC44A1):c.1182G>C (p.Trp394Cys) rs2538263048
NM_080546.5(SLC44A1):c.1204T>C (p.Cys402Arg)
NM_080546.5(SLC44A1):c.1309C>T (p.Arg437Cys) rs748507423
NM_080546.5(SLC44A1):c.13A>G (p.Ser5Gly)
NM_080546.5(SLC44A1):c.1429T>C (p.Cys477Arg) rs1827941782
NM_080546.5(SLC44A1):c.1769A>T (p.Tyr590Phe) rs2538311430
NM_080546.5(SLC44A1):c.1775T>C (p.Met592Thr)
NM_080546.5(SLC44A1):c.1808T>C (p.Ile603Thr)
NM_080546.5(SLC44A1):c.223A>G (p.Lys75Glu) rs368046201
NM_080546.5(SLC44A1):c.22T>A (p.Ser8Thr) rs1018350024
NM_080546.5(SLC44A1):c.260C>A (p.Thr87Asn)
NM_080546.5(SLC44A1):c.275T>C (p.Val92Ala)
NM_080546.5(SLC44A1):c.286G>A (p.Asp96Asn) rs1278798998
NM_080546.5(SLC44A1):c.296A>G (p.Asn99Ser)
NM_080546.5(SLC44A1):c.386A>G (p.Gln129Arg)
NM_080546.5(SLC44A1):c.436C>T (p.Pro146Ser) rs74511615
NM_080546.5(SLC44A1):c.451A>G (p.Thr151Ala)
NM_080546.5(SLC44A1):c.463T>C (p.Ser155Pro)
NM_080546.5(SLC44A1):c.482A>G (p.Lys161Arg)
NM_080546.5(SLC44A1):c.551A>G (p.Tyr184Cys)
NM_080546.5(SLC44A1):c.628A>G (p.Thr210Ala) rs2538238015
NM_080546.5(SLC44A1):c.764G>C (p.Gly255Ala)
NM_080546.5(SLC44A1):c.893T>C (p.Val298Ala)
NM_080546.5(SLC44A1):c.932G>A (p.Arg311His)

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