List of variants in gene ARHGAP31 reported as benign for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_020754.4(ARHGAP31):c.2407G>A (p.Gly803Ser)	rs3732413	0.83326
NM_020754.4(ARHGAP31):c.1926+5A>G	rs1463139	0.65459
NM_020754.4(ARHGAP31):c.1926+11T>C	rs1463138	0.48304
NM_020754.4(ARHGAP31):c.100+77A>T	rs3732412	0.47316
NM_020754.4(ARHGAP31):c.1926+89T>A	rs12636976	0.38289
NM_020754.4(ARHGAP31):c.1070-92G>C	rs10511390	0.30391
NM_020754.4(ARHGAP31):c.1701G>A (p.Pro567=)	rs2305249	0.15274
NM_020754.4(ARHGAP31):c.2778G>A (p.Ala926=)	rs61740281	0.13242
NM_020754.4(ARHGAP31):c.3615C>T (p.Pro1205=)	rs3732414	0.11988
NM_020754.4(ARHGAP31):c.-38C>A	rs72960626	0.08337
NM_020754.4(ARHGAP31):c.540-6C>T	rs16829782	0.06792
NM_020754.4(ARHGAP31):c.432-100T>A	rs73187863	0.06662
NM_020754.4(ARHGAP31):c.881+7G>A	rs78837524	0.05414
NM_020754.4(ARHGAP31):c.1533A>G (p.Thr511=)	rs77678258	0.02008
NM_020754.4(ARHGAP31):c.1700C>T (p.Pro567Leu)	rs61744178	0.01996
NM_020754.4(ARHGAP31):c.1491C>A (p.Arg497=)	rs61747387	0.01984
NM_020754.4(ARHGAP31):c.1614A>G (p.Glu538=)	rs61744411	0.01720
NM_020754.4(ARHGAP31):c.682+19A>C	rs72966429	0.01642
NM_020754.4(ARHGAP31):c.432-7A>G	rs10049221	0.00871
NM_020754.4(ARHGAP31):c.3256G>A (p.Ala1086Thr)	rs61744168	0.00542
NM_020754.4(ARHGAP31):c.384G>C (p.Leu128=)	rs150339878	0.00503
NM_020754.4(ARHGAP31):c.1597G>A (p.Gly533Arg)	rs75764457	0.00387
NM_020754.4(ARHGAP31):c.820C>T (p.Pro274Ser)	rs139600783	0.00337
NM_020754.4(ARHGAP31):c.654C>T (p.Asn218=)	rs145326425	0.00294
NM_020754.4(ARHGAP31):c.349-7T>G	rs200397968	0.00173
NM_020754.4(ARHGAP31):c.1618A>G (p.Lys540Glu)	rs61744410	0.00172
NM_020754.4(ARHGAP31):c.936T>C (p.Arg312=)	rs200813566	0.00113
NM_020754.4(ARHGAP31):c.2359C>G (p.Pro787Ala)	rs186621177	0.00105
NM_020754.4(ARHGAP31):c.2364A>T (p.Pro788=)	rs61746581	0.00095
NM_020754.4(ARHGAP31):c.4096G>A (p.Val1366Met)	rs3796360	0.00031

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