ClinVar Miner

List of variants in gene SLC1A3 reported as likely benign for not provided

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Gene type:
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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_004172.5(SLC1A3):c.792G>A (p.Gly264=) rs139659178 0.00387
NM_004172.5(SLC1A3):c.*174del rs538321546 0.00368
NM_004172.5(SLC1A3):c.69T>A (p.Arg23=) rs140080134 0.00342
NM_004172.5(SLC1A3):c.1489T>C (p.Leu497=) rs150357327 0.00272
NM_004172.5(SLC1A3):c.*1206G>A rs530235885 0.00146
NM_004172.5(SLC1A3):c.1074C>T (p.Thr358=) rs147973032 0.00068
NM_004172.5(SLC1A3):c.320-7C>T rs200867287 0.00063
NM_004172.5(SLC1A3):c.15T>C (p.Asn5=) rs143791614 0.00061
NM_004172.5(SLC1A3):c.1154G>A (p.Arg385His) rs115702388 0.00058
NM_004172.5(SLC1A3):c.648T>C (p.Asn216=) rs139342707 0.00045
NM_004172.5(SLC1A3):c.68G>A (p.Arg23His) rs199774340 0.00026
NM_004172.5(SLC1A3):c.231A>G (p.Glu77=) rs141828644 0.00023
NM_004172.5(SLC1A3):c.1425-8G>C rs202233020 0.00016
NM_004172.5(SLC1A3):c.676C>G (p.Arg226Gly) rs201069745 0.00016
NM_004172.5(SLC1A3):c.182-8T>C rs758803628 0.00015
NM_004172.5(SLC1A3):c.985G>A (p.Ala329Thr) rs200243548 0.00013
NM_004172.5(SLC1A3):c.796G>A (p.Ala266Thr) rs146929198 0.00012
NM_004172.5(SLC1A3):c.1284A>C (p.Thr428=) rs200947079 0.00006
NM_004172.5(SLC1A3):c.1496G>A (p.Arg499Gln) rs138085358 0.00006
NM_004172.5(SLC1A3):c.36G>A (p.Gly12=) rs752951426 0.00006
NM_004172.5(SLC1A3):c.952A>G (p.Thr318Ala) rs117588697 0.00005
NM_004172.5(SLC1A3):c.188T>C (p.Ile63Thr) rs138559945 0.00004
NM_004172.5(SLC1A3):c.1434C>G (p.Leu478=) rs778865549 0.00002
NM_004172.5(SLC1A3):c.897G>A (p.Gly299=) rs768627283 0.00002
NM_004172.5(SLC1A3):c.102G>A (p.Gln34=) rs765939940 0.00001
NM_004172.5(SLC1A3):c.825C>T (p.Asn275=) rs201765665 0.00001
NM_004172.5(SLC1A3):c.993C>T (p.Ile331=) rs768494940 0.00001
NM_004172.5(SLC1A3):c.1065A>T (p.Ala355=) rs765536752
NM_004172.5(SLC1A3):c.1080G>A (p.Leu360=)
NM_004172.5(SLC1A3):c.1094+11A>G
NM_004172.5(SLC1A3):c.1094+18G>A
NM_004172.5(SLC1A3):c.1149C>T (p.Asp383=)
NM_004172.5(SLC1A3):c.1155C>T (p.Arg385=)
NM_004172.5(SLC1A3):c.1176C>T (p.Pro392=)
NM_004172.5(SLC1A3):c.1289+15T>A
NM_004172.5(SLC1A3):c.1289+20T>C
NM_004172.5(SLC1A3):c.1338G>A (p.Ala446=)
NM_004172.5(SLC1A3):c.1356C>T (p.Val452=)
NM_004172.5(SLC1A3):c.1359T>C (p.Ile453=)
NM_004172.5(SLC1A3):c.1374C>T (p.Val458=)
NM_004172.5(SLC1A3):c.1389C>T (p.Asp463=)
NM_004172.5(SLC1A3):c.1425-13A>C
NM_004172.5(SLC1A3):c.1446C>T (p.Thr482=) rs17853737
NM_004172.5(SLC1A3):c.1464C>T (p.Ser488=)
NM_004172.5(SLC1A3):c.156G>A (p.Leu52=)
NM_004172.5(SLC1A3):c.1608C>T (p.Ile536=)
NM_004172.5(SLC1A3):c.168C>T (p.Thr56=) rs751614772
NM_004172.5(SLC1A3):c.182-20T>C
NM_004172.5(SLC1A3):c.182-6dup
NM_004172.5(SLC1A3):c.182-9_182-8dup
NM_004172.5(SLC1A3):c.210A>G (p.Pro70=)
NM_004172.5(SLC1A3):c.221G>A (p.Ser74Asn)
NM_004172.5(SLC1A3):c.319+11C>G
NM_004172.5(SLC1A3):c.319+16G>A
NM_004172.5(SLC1A3):c.320-19T>G
NM_004172.5(SLC1A3):c.320-4C>A rs760934282
NM_004172.5(SLC1A3):c.320-9C>T
NM_004172.5(SLC1A3):c.330G>A (p.Ala110=)
NM_004172.5(SLC1A3):c.396C>T (p.Ile132=)
NM_004172.5(SLC1A3):c.462C>T (p.Asn154=)
NM_004172.5(SLC1A3):c.498T>C (p.Ala166=)
NM_004172.5(SLC1A3):c.524+19G>A
NM_004172.5(SLC1A3):c.524+9T>C
NM_004172.5(SLC1A3):c.568-11T>C
NM_004172.5(SLC1A3):c.568-19_568-17del
NM_004172.5(SLC1A3):c.618C>T (p.Asn206=)
NM_004172.5(SLC1A3):c.624G>A (p.Thr208=)
NM_004172.5(SLC1A3):c.760G>A (p.Gly254Ser)
NM_004172.5(SLC1A3):c.801G>A (p.Leu267=) rs1040061193
NM_004172.5(SLC1A3):c.849A>C (p.Ala283=)
NM_004172.5(SLC1A3):c.861-12G>T
NM_004172.5(SLC1A3):c.870C>T (p.Pro290=)
NM_004172.5(SLC1A3):c.984C>T (p.His328=)

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