List of variants reported as likely pathogenic for Androgen resistance syndrome

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Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_000044.6(AR):c.1181_1200dup (p.Ala401fs)
NM_000044.6(AR):c.1341T>A (p.Tyr447Ter)
NM_000044.6(AR):c.1396_1397insAG (p.Gly466fs)
NM_000044.6(AR):c.1605del (p.Pro534_Tyr535insTer)
NM_000044.6(AR):c.1616+1_1616+3delinsT
NM_000044.6(AR):c.1685T>C (p.Ile562Thr)	rs886041050
NM_000044.6(AR):c.1715A>G (p.Tyr572Cys)	rs1925886715
NM_000044.6(AR):c.1737C>A (p.Ser579Arg)
NM_000044.6(AR):c.1742A>C (p.Lys581Thr)	rs2147436623
NM_000044.6(AR):c.1749C>G (p.Phe583Leu)
NM_000044.6(AR):c.1762G>C (p.Ala588Pro)	rs1034866440
NM_000044.6(AR):c.1768+1G>A	rs2147436755
NM_000044.6(AR):c.1846C>T (p.Arg616Cys)	rs1555990485
NM_000044.6(AR):c.1873A>G (p.Met625Val)
NM_000044.6(AR):c.1933G>T (p.Glu645Ter)
NM_000044.6(AR):c.2072A>G (p.Asp691Gly)
NM_000044.6(AR):c.2076C>A (p.Asn692Lys)	rs2147524930
NM_000044.6(AR):c.2079C>G (p.Asn693Lys)
NM_000044.6(AR):c.2086G>A (p.Asp696Asn)	rs1555995840
NM_000044.6(AR):c.2090C>A (p.Ser697Tyr)	rs1555995842
NM_000044.6(AR):c.2159C>T (p.Ala720Val)	rs2076094679
NM_000044.6(AR):c.2170C>T (p.Pro724Ser)	rs2147525357
NM_000044.6(AR):c.2221T>C (p.Ser741Pro)
NM_000044.6(AR):c.2255G>C (p.Trp752Ser)	rs2147530924
NM_000044.6(AR):c.2339G>C (p.Arg780Pro)
NM_000044.6(AR):c.2342T>A (p.Met781Lys)	rs2076137339
NM_000044.6(AR):c.2449+1G>A
NM_000044.6(AR):c.2449+1_2449+3dup
NM_000044.6(AR):c.2567G>A (p.Arg856His)	rs9332971
NM_000044.6(AR):c.2570_2572del (p.Phe857del)	rs2076142436
NM_000044.6(AR):c.2636T>C (p.Phe879Ser)
NM_000044.6(AR):c.2710G>T (p.Val904Leu)	rs2147540656
NM_000044.6(AR):c.2747A>C (p.Tyr916Ser)	rs2076147482
NM_000044.6(AR):c.35del (p.Pro12fs)

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