ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_001723.7(DST):c.4980A>C (p.Val1660=) rs2230863 0.03282
NM_001723.7(DST):c.5055T>C (p.Asn1685=) rs2230864 0.03211
NM_001723.7(DST):c.7765A>G (p.Ile2589Val) rs150191284 0.02534
NM_001723.7(DST):c.6633A>G (p.Ala2211=) rs115542549 0.02533
NM_001374736.1(DST):c.4452T>C (p.Asn1484=) rs112640831 0.02508
NM_001374736.1(DST):c.4590T>G (p.Asn1530Lys) rs35014998 0.02397
NM_001723.7(DST):c.3346C>T (p.His1116Tyr) rs6909714 0.02098
NM_001723.7(DST):c.3809A>G (p.Lys1270Arg) rs35497571 0.02037
NM_001374736.1(DST):c.4062C>T (p.Val1354=) rs78600049 0.01311
NM_001374736.1(DST):c.3492C>T (p.Asn1164=) rs79026338 0.01176
NM_001723.7(DST):c.4289C>T (p.Ala1430Val) rs78701610 0.01093
NM_001723.7(DST):c.5485C>G (p.Gln1829Glu) rs79943354 0.01087
NM_001374736.1(DST):c.4831-3C>A rs115890942 0.01035
NM_001374736.1(DST):c.4200A>G (p.Lys1400=) rs35715547 0.00947
NM_001374736.1(DST):c.4930-300A>T rs75951731 0.00849
NM_001723.7(DST):c.4674C>T (p.Leu1558=) rs191617697 0.00285

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