ClinVar Miner

Variants in gene DST with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 25
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HGVS dbSNP gnomAD frequency
NM_001723.7(DST):c.3336G>C (p.Glu1112Asp) rs34767818 0.00349
NM_001374736.1(DST):c.2256A>T (p.Ser752=) rs113432929 0.00225
NM_001723.7(DST):c.4961C>T (p.Ala1654Val) rs150229184 0.00182
NM_001723.7(DST):c.4060C>A (p.Gln1354Lys) rs35599167 0.00167
NM_001374736.1(DST):c.2350C>G (p.Pro784Ala) rs151271595 0.00152
NM_001374736.1(DST):c.21538A>G (p.Met7180Val) rs200006386 0.00141
NM_001723.7(DST):c.4049C>T (p.Thr1350Met) rs45472691 0.00137
NM_001374736.1(DST):c.18433C>T (p.Arg6145Trp) rs193252082 0.00107
NM_001374736.1(DST):c.16495A>T (p.Ser5499Cys) rs180765536 0.00102
NM_001374736.1(DST):c.20438A>G (p.Asn6813Ser) rs199628430 0.00095
NM_001374736.1(DST):c.12043A>T (p.Ile4015Phe) rs201249286 0.00057
NM_001374736.1(DST):c.2125A>G (p.Met709Val) rs142650835 0.00039
NM_001374736.1(DST):c.5203A>G (p.Ser1735Gly) rs369218541 0.00024
NM_001374736.1(DST):c.13361T>C (p.Leu4454Ser) rs201758531 0.00014
NM_001374736.1(DST):c.3853A>G (p.Asn1285Asp) rs201419873 0.00012
NM_001374736.1(DST):c.23035G>T (p.Ala7679Ser) rs201138592 0.00009
NM_001374736.1(DST):c.15489G>C (p.Glu5163Asp) rs186788522 0.00006
NM_001374736.1(DST):c.2860-4G>C rs370134977 0.00005
NM_001374736.1(DST):c.17894A>C (p.Glu5965Ala) rs753007435 0.00001
NM_001374736.1(DST):c.1872T>G (p.Ser624=) rs994026153 0.00001
NM_001374736.1(DST):c.19415A>G (p.Lys6472Arg) rs904996327 0.00001
NM_001374736.1(DST):c.14441-7_14441-6del rs773495985
NM_001374736.1(DST):c.20916C>T (p.Tyr6972=) rs763815018
NM_001374736.1(DST):c.23195-6C>T
NM_001374736.1(DST):c.23348G>C (p.Arg7783Thr)

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