ClinVar Miner

List of variants in gene SLC6A5 reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_004211.5(SLC6A5):c.1230A>G (p.Ser410=) rs7925597 0.99649
NM_004211.5(SLC6A5):c.485C>G (p.Ala162Gly) rs1443549 0.99417
NM_004211.5(SLC6A5):c.371T>C (p.Phe124Ser) rs1443548 0.79432
NM_004211.5(SLC6A5):c.304G>A (p.Gly102Ser) rs1443547 0.36761
NM_004211.5(SLC6A5):c.2103G>A (p.Glu701=) rs2276433 0.35869
NM_004211.5(SLC6A5):c.352C>T (p.Leu118=) rs2241941 0.33160
NM_004211.5(SLC6A5):c.336C>T (p.Ser112=) rs7109418 0.25043
NM_004211.5(SLC6A5):c.1387G>A (p.Asp463Asn) rs1805091 0.22232
NM_004211.5(SLC6A5):c.*3C>T rs1401793 0.21907
NM_004211.5(SLC6A5):c.2239-6T>C rs2276432 0.17430
NM_004211.5(SLC6A5):c.2071-3C>A rs72932998 0.14713
NM_004211.5(SLC6A5):c.1371G>C (p.Lys457Asn) rs3740870 0.11591
NM_004211.4(SLC6A5):c.-176T>G rs58405430 0.11559
NM_004211.5(SLC6A5):c.1499+15T>C rs80286799 0.08830
NM_004211.5(SLC6A5):c.-33C>T rs76857783 0.08596
NM_004211.5(SLC6A5):c.951G>A (p.Thr317=) rs1443551 0.07046
NM_004211.5(SLC6A5):c.777A>G (p.Pro259=) rs34505618 0.03460
NM_004211.4(SLC6A5):c.-192C>T rs7952227 0.03201
NM_004211.5(SLC6A5):c.266C>A (p.Ala89Glu) rs61736602 0.02191
NM_004211.5(SLC6A5):c.500C>A (p.Thr167Lys) rs61736603 0.01875
NM_004211.5(SLC6A5):c.1496A>T (p.Tyr499Phe) rs7944684 0.01483
NM_004211.5(SLC6A5):c.347A>G (p.Asn116Ser) rs61736604 0.01473
NM_004211.5(SLC6A5):c.2299G>A (p.Gly767Arg) rs16906628 0.01434
NM_004211.5(SLC6A5):c.395C>G (p.Ala132Gly) rs34243519

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