List of variants in gene ARHGEF10 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_014629.4(ARHGEF10):c.1110G>C (p.Leu370Phe)	rs9657362	0.11648
NM_014629.4(ARHGEF10):c.1113C>T (p.Phe371=)	rs34655804	0.04733
NM_014629.4(ARHGEF10):c.2098G>A (p.Val700Ile)	rs2294039	0.03098
NM_014629.4(ARHGEF10):c.1991T>C (p.Met664Thr)	rs34319003	0.00800
NM_014629.4(ARHGEF10):c.1260+4C>T	rs79548709	0.00566
NM_014629.4(ARHGEF10):c.38-10T>C	rs138713415	0.00351
NM_014629.4(ARHGEF10):c.401C>T (p.Ala134Val)	rs151080025	0.00082
NM_014629.4(ARHGEF10):c.474C>T (p.Asp158=)	rs147914724	0.00082
NM_014629.4(ARHGEF10):c.3869C>T (p.Ser1290Leu)	rs150226594	0.00041
NM_014629.4(ARHGEF10):c.2909C>T (p.Thr970Met)	rs35925274	0.00036
NM_014629.4(ARHGEF10):c.2728A>G (p.Ile910Val)	rs1480757811	0.00003
NM_014629.4(ARHGEF10):c.1911A>G (p.Lys637=)	rs1222847857
NM_014629.4(ARHGEF10):c.831C>G (p.Asn277Lys)	rs756594069

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