List of variants in gene FAM76B

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_144664.5(FAM76B):c.533A>C (p.His178Pro)	rs200906102	0.00009
NM_144664.5(FAM76B):c.894G>C (p.Met298Ile)	rs925026952	0.00003
NM_144664.5(FAM76B):c.527A>G (p.His176Arg)	rs771402543	0.00002
NM_144664.5(FAM76B):c.935A>G (p.Lys312Arg)	rs780571127	0.00002
NM_144664.5(FAM76B):c.628A>G (p.Thr210Ala)	rs777299820	0.00001
NM_144664.5(FAM76B):c.1000A>G (p.Ser334Gly)
NM_144664.5(FAM76B):c.121A>C (p.Thr41Pro)	rs1860734253
NM_144664.5(FAM76B):c.341G>A (p.Arg114Gln)
NM_144664.5(FAM76B):c.378A>C (p.Leu126Phe)	rs762532217
NM_144664.5(FAM76B):c.431A>G (p.Glu144Gly)
NM_144664.5(FAM76B):c.458A>G (p.His153Arg)	rs778189566
NM_144664.5(FAM76B):c.484A>G (p.Thr162Ala)	rs61749525
NM_144664.5(FAM76B):c.551G>A (p.Ser184Asn)	rs2496674446
NM_144664.5(FAM76B):c.596G>C (p.Gly199Ala)
NM_144664.5(FAM76B):c.700A>G (p.Ile234Val)
NM_144664.5(FAM76B):c.771G>A (p.Met257Ile)
NM_144664.5(FAM76B):c.931G>A (p.Ala311Thr)

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