ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance by Genesis Genome Database

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.13088A>C (p.Lys4363Thr) rs141925609 0.00002
NM_001376.5(DYNC1H1):c.13795G>A (p.Glu4599Lys) rs753454594 0.00001
NM_001376.5(DYNC1H1):c.13912C>T (p.Arg4638Trp) rs200224597 0.00001
NM_001376.5(DYNC1H1):c.11402A>C (p.Tyr3801Ser) rs1595629587
NM_001376.5(DYNC1H1):c.11416A>C (p.Thr3806Pro) rs1595629612
NM_001376.5(DYNC1H1):c.11618G>C (p.Arg3873Pro) rs745812006
NM_001376.5(DYNC1H1):c.12763C>G (p.Arg4255Gly) rs770105370
NM_001376.5(DYNC1H1):c.12767T>G (p.Val4256Gly) rs1298640455
NM_001376.5(DYNC1H1):c.13166A>G (p.His4389Arg) rs1206639344
NM_001376.5(DYNC1H1):c.13565C>T (p.Thr4522Ile) rs1595637702
NM_001376.5(DYNC1H1):c.148del (p.Ala50fs) rs1595590195
NM_001376.5(DYNC1H1):c.149C>A (p.Ala50Asp) rs1350501046
NM_001376.5(DYNC1H1):c.248C>T (p.Thr83Met) rs1400787976
NM_001376.5(DYNC1H1):c.3574A>C (p.Asn1192His) rs1265590172
NM_001376.5(DYNC1H1):c.3845T>G (p.Ile1282Arg) rs1479995920
NM_001376.5(DYNC1H1):c.6023T>G (p.Val2008Gly) rs1595613980
NM_001376.5(DYNC1H1):c.6222-4C>T rs1382280530
NM_001376.5(DYNC1H1):c.6406-4G>A rs374602014
NM_001376.5(DYNC1H1):c.6728G>T (p.Arg2243Ile) rs1595615102
NM_001376.5(DYNC1H1):c.7931C>T (p.Thr2644Ile) rs1595617838
NM_001376.5(DYNC1H1):c.7979T>G (p.Val2660Gly) rs201272954
NM_001376.5(DYNC1H1):c.9703G>C (p.Ala3235Pro) rs199966256
NM_001376.5(DYNC1H1):c.9858A>C (p.Glu3286Asp) rs756906168

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