"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC109504 - ClinVar - NCBI

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Search results

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043532	NM_000044.6(AR):c.170_184del (p.Leu57_Gln61del)	AR, LOC109504725	Deletion (inframe_deletion +1 more)	AR-related disorder	GBenign
Select item 1285161	NM_000044.6(AR):c.171GCA[29] (p.Gln75_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	AR-related disorder +1 more	GBenign
Select item 1200448	NM_000044.6(AR):c.171GCA[34] (p.Gln70_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1168151	NM_000044.6(AR):c.171GCA[27] (p.Gln77_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	Androgen resistance syndrome +3 more	GBenign/Likely benign
Select item 507868	NM_000044.6(AR):c.171GCA[30] (p.Gln74_Gln80dup)	AR, LOC109504725	Microsatellite (inframe_insertion +1 more)	AR-related disorder +3 more	GBenign/Likely benign
Select item 3053691	NM_000044.6(AR):c.171GCA[9] (p.Gln67_Gln80del)	AR, LOC109504725	Microsatellite (inframe deletion +2 more)	AR-related disorder	GBenign
Select item 3047828	NM_000044.6(AR):c.171GCA[8] (p.Gln66_Gln80del)	AR, LOC109504725	Microsatellite (inframe deletion +2 more)	AR-related disorder	GLikely benign
Select item 1556388	NM_000044.6(AR):c.171GCA[11] (p.Gln69_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	AR-related disorder +2 more	GBenign/Likely benign
Select item 1166167	NM_000044.6(AR):c.171GCA[13] (p.Gln71_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not provided +3 more	GBenign/Likely benign
Select item 516217	NM_000044.6(AR):c.171GCA[14] (p.Gln72_Gln80del)	AR, LOC109504725	Microsatellite (inframe_deletion +1 more)	not specified +7 more	GBenign/Likely benign