ClinVar Miner

List of variants in gene HSD17B10 reported as likely benign for not provided

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Gene type:
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Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_004493.3(HSD17B10):c.28-140C>T rs139681190 0.00980
NC_000023.11:g.53434487G>T rs181636967 0.00571
NM_004493.3(HSD17B10):c.239G>C (p.Gly80Ala) rs781891910 0.00014
NM_004493.3(HSD17B10):c.147C>G (p.Ala49=) rs367982176 0.00010
NM_004493.3(HSD17B10):c.358-13A>G rs782644415 0.00005
NM_004493.3(HSD17B10):c.273T>C (p.Cys91=) rs782330394 0.00004
NM_004493.3(HSD17B10):c.144G>A (p.Glu48=) rs782158864 0.00003
NM_004493.3(HSD17B10):c.486+9G>A rs190913381 0.00003
NM_004493.3(HSD17B10):c.27+7G>A rs941613640 0.00002
NM_004493.3(HSD17B10):c.201T>C (p.Ser67=) rs1343698835 0.00001
NM_004493.3(HSD17B10):c.27+20T>G rs1307768787 0.00001
NM_004493.3(HSD17B10):c.357+11G>A rs781979081 0.00001
NM_004493.3(HSD17B10):c.487-6C>T rs374264193 0.00001
NM_004493.3(HSD17B10):c.102A>T (p.Gly34=)
NM_004493.3(HSD17B10):c.12G>T (p.Ala4=)
NM_004493.3(HSD17B10):c.141G>A (p.Gly47=)
NM_004493.3(HSD17B10):c.15T>C (p.Cys5=)
NM_004493.3(HSD17B10):c.16C>A (p.Arg6=)
NM_004493.3(HSD17B10):c.171C>T (p.Asn57=)
NM_004493.3(HSD17B10):c.180C>T (p.Phe60=) rs1569366312
NM_004493.3(HSD17B10):c.189C>T (p.Ala63=)
NM_004493.3(HSD17B10):c.192+12C>G
NM_004493.3(HSD17B10):c.192+14C>T
NM_004493.3(HSD17B10):c.192+7G>A
NM_004493.3(HSD17B10):c.193-10_193-7del
NM_004493.3(HSD17B10):c.193-12CT[2]
NM_004493.3(HSD17B10):c.193-16A>G
NM_004493.3(HSD17B10):c.193-4G>A
NM_004493.3(HSD17B10):c.195G>A (p.Val65=)
NM_004493.3(HSD17B10):c.240A>C (p.Gly80=)
NM_004493.3(HSD17B10):c.243G>A (p.Lys81=) rs2146628349
NM_004493.3(HSD17B10):c.27+10T>C
NM_004493.3(HSD17B10):c.27+17C>G
NM_004493.3(HSD17B10):c.27+17C>T
NM_004493.3(HSD17B10):c.27+19C>G
NM_004493.3(HSD17B10):c.276A>C (p.Ala92=)
NM_004493.3(HSD17B10):c.279C>T (p.Gly93=)
NM_004493.3(HSD17B10):c.28-16A>G
NM_004493.3(HSD17B10):c.28-20G>A
NM_004493.3(HSD17B10):c.28-4A>T
NM_004493.3(HSD17B10):c.28-6T>C rs1827330997
NM_004493.3(HSD17B10):c.285G>A (p.Ala95=)
NM_004493.3(HSD17B10):c.288G>A (p.Val96=)
NM_004493.3(HSD17B10):c.300G>A (p.Thr100=)
NM_004493.3(HSD17B10):c.303C>T (p.Tyr101=)
NM_004493.3(HSD17B10):c.307T>C (p.Leu103=)
NM_004493.3(HSD17B10):c.314A>C (p.Lys105Thr) rs2075827990
NM_004493.3(HSD17B10):c.318C>A (p.Gly106=)
NM_004493.3(HSD17B10):c.318C>T (p.Gly106=)
NM_004493.3(HSD17B10):c.330C>G (p.Thr110=)
NM_004493.3(HSD17B10):c.33G>A (p.Leu11=)
NM_004493.3(HSD17B10):c.354T>A (p.Leu118=)
NM_004493.3(HSD17B10):c.357T>C (p.Asp119=)
NM_004493.3(HSD17B10):c.358-11C>G
NM_004493.3(HSD17B10):c.358-15C>T
NM_004493.3(HSD17B10):c.39G>C (p.Ala13=)
NM_004493.3(HSD17B10):c.444G>C (p.Gly148=)
NM_004493.3(HSD17B10):c.450C>T (p.Ile150=)
NM_004493.3(HSD17B10):c.453C>T (p.Ile151=)
NM_004493.3(HSD17B10):c.477C>T (p.Phe159=)
NM_004493.3(HSD17B10):c.486+19G>A
NM_004493.3(HSD17B10):c.487-10C>G
NM_004493.3(HSD17B10):c.487-13A>C
NM_004493.3(HSD17B10):c.487-13A>G
NM_004493.3(HSD17B10):c.487-15C>A
NM_004493.3(HSD17B10):c.487-16T>C
NM_004493.3(HSD17B10):c.487-18C>T
NM_004493.3(HSD17B10):c.531C>A (p.Gly177=)
NM_004493.3(HSD17B10):c.543C>T (p.Pro181=)
NM_004493.3(HSD17B10):c.595+12C>T
NM_004493.3(HSD17B10):c.595+17_595+20del rs782819364
NM_004493.3(HSD17B10):c.595+8T>C
NM_004493.3(HSD17B10):c.596-11A>G
NM_004493.3(HSD17B10):c.596-13C>T
NM_004493.3(HSD17B10):c.596-19A>T
NM_004493.3(HSD17B10):c.596-8T>C
NM_004493.3(HSD17B10):c.636A>G (p.Lys212=)
NM_004493.3(HSD17B10):c.666C>T (p.Pro222=)
NM_004493.3(HSD17B10):c.693T>A (p.Ala231=)
NM_004493.3(HSD17B10):c.6A>C (p.Ala2=) rs897323903
NM_004493.3(HSD17B10):c.6A>G (p.Ala2=)
NM_004493.3(HSD17B10):c.708C>T (p.Leu236=)
NM_004493.3(HSD17B10):c.711A>G (p.Val237=)
NM_004493.3(HSD17B10):c.723C>T (p.Ile241=)
NM_004493.3(HSD17B10):c.741T>C (p.Asn247=)
NM_004493.3(HSD17B10):c.750C>T (p.Val250=)
NM_004493.3(HSD17B10):c.774T>C (p.Arg258=)
NM_004493.3(HSD17B10):c.78G>A (p.Thr26=)
NM_004493.3(HSD17B10):c.90T>C (p.Leu30=)
NM_004493.3(HSD17B10):c.90T>G (p.Leu30=)

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