List of variants in gene CYP17A1 reported as likely benign for adrenocortical insufficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000102.4(CYP17A1):c.1243+113A>T	rs10883783	0.24865
NM_000102.4(CYP17A1):c.1139+19T>G	rs4919686	0.21485
NM_000102.4(CYP17A1):c.1243+83C>A	rs284849	0.15759
NM_000102.4(CYP17A1):c.1458C>T (p.Ile486=)	rs147557447	0.00023
NM_000102.4(CYP17A1):c.32C>T (p.Thr11Ile)	rs72559703	0.00009
NM_000102.4(CYP17A1):c.1194G>A (p.Ala398=)	rs201222065	0.00008
NM_000102.4(CYP17A1):c.831T>C (p.Asn277=)	rs1043151688	0.00003
NM_000102.4(CYP17A1):c.654C>T (p.Val218=)	rs375350911	0.00002
NM_000102.4(CYP17A1):c.1233G>A (p.Gln411=)	rs755050448	0.00001
NM_000102.4(CYP17A1):c.276C>T (p.Asp92=)	rs535575638	0.00001
NM_000102.4(CYP17A1):c.318C>T (p.Ser106=)	rs766679884	0.00001
NM_000102.4(CYP17A1):c.741T>C (p.Leu247=)	rs778591928	0.00001
NM_000102.4(CYP17A1):c.180T>C (p.Tyr60=)	rs61754264
NM_000102.4(CYP17A1):c.186C>T (p.Pro62=)	rs1844174531
NM_000102.4(CYP17A1):c.315G>A (p.Ala105=)	rs150698224

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