ClinVar Miner

List of variants in gene OR10H1 reported as uncertain significance for not specified

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_013940.4(OR10H1):c.704G>A (p.Arg235Gln) rs143909032 0.00025
NM_013940.4(OR10H1):c.431T>G (p.Leu144Arg) rs559894657 0.00017
NM_013940.4(OR10H1):c.676A>G (p.Ile226Val) rs147258134 0.00005
NM_013940.4(OR10H1):c.751G>A (p.Val251Met) rs569257281 0.00002
NM_013940.4(OR10H1):c.187C>G (p.Leu63Val) rs752066788 0.00001
NM_013940.4(OR10H1):c.307T>C (p.Phe103Leu) rs1427822593 0.00001
NM_013940.4(OR10H1):c.392G>A (p.Arg131His) rs527762025 0.00001
NM_013940.4(OR10H1):c.436G>A (p.Gly146Ser) rs1450627724 0.00001
NM_013940.4(OR10H1):c.524A>T (p.His175Leu) rs1247777702 0.00001
NM_013940.4(OR10H1):c.758A>G (p.Tyr253Cys) rs1427977137 0.00001
NM_013940.4(OR10H1):c.119T>A (p.Leu40Gln)
NM_013940.4(OR10H1):c.153C>G (p.Ser51Arg)
NM_013940.4(OR10H1):c.170C>T (p.Thr57Met)
NM_013940.4(OR10H1):c.236C>T (p.Pro79Leu)
NM_013940.4(OR10H1):c.268C>G (p.Arg90Gly)
NM_013940.4(OR10H1):c.274A>T (p.Ile92Phe)
NM_013940.4(OR10H1):c.320T>C (p.Phe107Ser)
NM_013940.4(OR10H1):c.349G>C (p.Val117Leu)
NM_013940.4(OR10H1):c.35T>A (p.Phe12Tyr) rs2512579936
NM_013940.4(OR10H1):c.361G>C (p.Asp121His)
NM_013940.4(OR10H1):c.380G>C (p.Cys127Ser) rs1352307531
NM_013940.4(OR10H1):c.400G>C (p.Val134Leu) rs141400861
NM_013940.4(OR10H1):c.400G>T (p.Val134Leu) rs141400861
NM_013940.4(OR10H1):c.407T>G (p.Met136Arg) rs1363398317
NM_013940.4(OR10H1):c.416G>C (p.Arg139Pro)
NM_013940.4(OR10H1):c.458T>G (p.Leu153Trp)
NM_013940.4(OR10H1):c.463A>G (p.Met155Val) rs2512579185
NM_013940.4(OR10H1):c.476T>C (p.Val159Ala) rs2512579157
NM_013940.4(OR10H1):c.500C>A (p.Ala167Asp) rs2512579123
NM_013940.4(OR10H1):c.55G>A (p.Val19Ile) rs2512579899
NM_013940.4(OR10H1):c.592A>C (p.Lys198Gln) rs2512578965
NM_013940.4(OR10H1):c.608T>C (p.Val203Ala)
NM_013940.4(OR10H1):c.736C>T (p.Leu246Phe)
NM_013940.4(OR10H1):c.749T>C (p.Val250Ala)
NM_013940.4(OR10H1):c.862C>T (p.Pro288Ser)
NM_013940.4(OR10H1):c.914C>T (p.Thr305Ile)

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