ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510, LOC110006319 reported as other

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_000518.4(HBB):c.302C>G (p.Pro101Arg) rs33965000
NM_000518.4(HBB):c.302C>T (p.Pro101Leu) rs33965000
NM_000518.4(HBB):c.304G>A (p.Glu102Lys) rs33966487
NM_000518.4(HBB):c.304G>C (p.Glu102Gln) rs33966487
NM_000518.4(HBB):c.308A>G (p.Asn103Ser) rs33948057
NM_000518.4(HBB):c.310T>A (p.Phe104Ile) rs33921589
NM_000518.4(HBB):c.310T>G (p.Phe104Val) rs33921589
NM_000518.4(HBB):c.[197A>T;367T>C]
NM_000518.4(HBB):c.[278A>C;315G>Y]
NM_000518.4(HBB):c.[280T>C;364G>C]
NM_000518.4(HBB):c.[29C>A;364G>C]
NM_000518.4(HBB):c.[34G>A;364G>A]
NM_000518.4(HBB):c.[364G>C;79G>A]
NM_000518.5(HBB):c.305A>G (p.Glu102Gly) rs33937393
NM_000518.5(HBB):c.306G>C (p.Glu102Asp) rs35209591
NM_000518.5(HBB):c.307A>T (p.Asn103Tyr) rs33927739
NM_000518.5(HBB):c.312C>G (p.Phe104Leu) rs35067717
NM_000518.5(HBB):c.314G>C (p.Arg105Thr) rs33911434
NM_000518.5(HBB):c.315G>Y (p.Arg105Ser) rs33914944

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