ClinVar Miner

List of variants in gene RB1 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_000321.2(RB1):c.*1022C>T rs886050283
NM_000321.2(RB1):c.*1459T>C rs886050284
NM_000321.2(RB1):c.*1540A>G rs768155412
NM_000321.2(RB1):c.*1544T>C rs886050285
NM_000321.2(RB1):c.*162T>G rs886050273
NM_000321.2(RB1):c.*1635T>A rs886050286
NM_000321.2(RB1):c.*398G>T rs886050274
NM_000321.2(RB1):c.*413T>G rs886050275
NM_000321.2(RB1):c.*435A>G rs886050276
NM_000321.2(RB1):c.*448_*451delATCT rs746086958
NM_000321.2(RB1):c.*512A>C rs886050278
NM_000321.2(RB1):c.*604A>T rs886050279
NM_000321.2(RB1):c.*673G>T rs886050280
NM_000321.2(RB1):c.*788C>A rs886050281
NM_000321.2(RB1):c.*998G>A rs886050282
NM_000321.2(RB1):c.-153G>T rs886050266
NM_000321.2(RB1):c.-156C>A rs886050265
NM_000321.2(RB1):c.-69G>C rs753117180
NM_000321.2(RB1):c.-81G>A rs886050267
NM_000321.2(RB1):c.2106+8A>G rs750581965
NM_000321.2(RB1):c.2652A>C (p.Glu884Asp) rs765537411
NM_000321.2(RB1):c.299G>C (p.Gly100Ala) rs886050268
NM_000321.2(RB1):c.393C>G (p.Phe131Leu) rs749495284
NM_000321.2(RB1):c.616T>C (p.Leu206=) rs886050270
NM_000321.2(RB1):c.953C>G (p.Ser318Cys) rs886050271

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