List of variants in gene ARHGAP31 reported by Eurofins NTD LLC (GA)

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: 27

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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.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.2344C>A (p.Pro782Thr)	rs139659618	0.00154
NM_020754.4(ARHGAP31):c.2814G>T (p.Gln938His)	rs201519258	0.00135
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.452G>A (p.Arg151Gln)	rs201519981	0.00069
NM_020754.4(ARHGAP31):c.4096G>A (p.Val1366Met)	rs3796360	0.00031
NM_020754.4(ARHGAP31):c.435C>G (p.Thr145=)	rs201927115	0.00024
NM_020754.4(ARHGAP31):c.2323G>A (p.Gly775Ser)	rs147415811	0.00022
NM_020754.4(ARHGAP31):c.499G>A (p.Ala167Thr)	rs139733647	0.00012
NM_020754.4(ARHGAP31):c.2216C>T (p.Pro739Leu)	rs200598971	0.00010
NM_020754.4(ARHGAP31):c.3461C>T (p.Pro1154Leu)	rs772715426	0.00010
NM_020754.4(ARHGAP31):c.3255C>T (p.Pro1085=)	rs372301689	0.00004
NM_020754.4(ARHGAP31):c.347C>T (p.Thr116Met)	rs756581922	0.00004
NM_020754.4(ARHGAP31):c.1824G>A (p.Pro608=)	rs760570856	0.00003
NM_020754.4(ARHGAP31):c.2412G>A (p.Pro804=)	rs776194035	0.00002
NM_020754.4(ARHGAP31):c.1430C>T (p.Pro477Leu)	rs200233879	0.00001
NM_020754.4(ARHGAP31):c.2611G>T (p.Val871Phe)	rs775132237
NM_020754.4(ARHGAP31):c.2792T>A (p.Val931Glu)	rs886044036
NM_020754.4(ARHGAP31):c.4121C>T (p.Ser1374Phe)	rs886043818
NM_020754.4(ARHGAP31):c.4194C>G (p.Val1398=)	rs1560000236
NM_020754.4(ARHGAP31):c.4218G>C (p.Arg1406Ser)	rs886043830

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