"PreventionGenetics, part of Exact Sciences"[submitter] AND "KANK2"[ge - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1554484	NM_001136191.3(KANK2):c.2512A>G (p.Met838Val)	KANK2 (M838V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3043500	NM_001136191.3(KANK2):c.2503-9_2503-8del	KANK2	Microsatellite (intron variant)	KANK2-related disorder	GLikely benign
Select item 2901169	NM_001136191.3(KANK2):c.2313C>T (p.Asp771=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder +1 more	GLikely benign
Select item 3040242	NM_001136191.3(KANK2):c.2298C>T (p.Asn766=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder	GLikely benign
Select item 1627096	NM_001136191.3(KANK2):c.2252G>A (p.Arg751Gln)	KANK2 (R751Q +1 more)	Single nucleotide variant (missense variant)	KANK2-related disorder +1 more	GLikely benign
Select item 2198558	NM_001136191.3(KANK2):c.2070T>C (p.Gly690=)	KANK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2414934	NM_001136191.3(KANK2):c.2043C>T (p.Pro681=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder +1 more	GLikely benign
Select item 2723213	NM_001136191.3(KANK2):c.1941G>A (p.Thr647=)	KANK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3050974	NM_001136191.3(KANK2):c.1924C>T (p.Arg642Trp)	KANK2 (R642W +1 more)	Single nucleotide variant (missense variant)	KANK2-related disorder	GUncertain significance
Select item 2073775	NM_001136191.3(KANK2):c.1914C>T (p.Pro638=)	KANK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1572287	NM_001136191.3(KANK2):c.1827C>A (p.Asn609Lys)	KANK2 (N609K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3048733	NM_001136191.3(KANK2):c.1728G>C (p.Gly576=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder	GLikely benign
Select item 738899	NM_001136191.3(KANK2):c.1676G>T (p.Arg559Leu)	KANK2 (R559L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3039611	NM_001136191.3(KANK2):c.1670C>G (p.Thr557Ser)	KANK2 (T557S +1 more)	Single nucleotide variant (missense variant)	KANK2-related disorder	GLikely benign
Select item 2178852	NM_001136191.3(KANK2):c.1611G>A (p.Arg537=)	KANK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3029122	NM_001136191.3(KANK2):c.1587C>T (p.Asn529=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder	GLikely benign
Select item 3036088	NM_001136191.3(KANK2):c.1521-7T>A	KANK2	Single nucleotide variant (intron variant)	KANK2-related disorder	GLikely benign
Select item 2899551	NM_001136191.3(KANK2):c.1485C>T (p.His495=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder +1 more	GLikely benign
Select item 3055381	NM_001136191.3(KANK2):c.1417+9T>C	KANK2	Single nucleotide variant (intron variant)	KANK2-related disorder	GLikely benign
Select item 2724574	NM_001136191.3(KANK2):c.1275G>A (p.Ser425=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder +1 more	GBenign/Likely benign
Select item 2137800	NM_001136191.3(KANK2):c.1274C>T (p.Ser425Leu)	KANK2 (S425L)	Single nucleotide variant (missense variant)	KANK2-related disorder +1 more	GLikely benign
Select item 1589638	NM_001136191.3(KANK2):c.1249+10C>T	KANK2	Single nucleotide variant (intron variant)	KANK2-related disorder +1 more	GLikely benign
Select item 3057580	NM_001136191.3(KANK2):c.1200T>C (p.His400=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder	GLikely benign
Select item 1510116	NM_001136191.3(KANK2):c.1138C>T (p.Arg380Cys)	KANK2 (R380C)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 2187911	NM_001136191.3(KANK2):c.1050C>G (p.Pro350=)	KANK2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3031756	NM_001136191.3(KANK2):c.987A>G (p.Thr329=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder	GLikely benign
Select item 3052107	NM_001136191.3(KANK2):c.678C>T (p.Leu226=)	KANK2	Single nucleotide variant (synonymous variant)	KANK2-related disorder	GLikely benign
Select item 2629359	NM_001136191.3(KANK2):c.628C>T (p.Pro210Ser)	KANK2 (P210S)	Single nucleotide variant (missense variant)	KANK2-related disorder	GUncertain significance
Select item 1317449	NM_001136191.3(KANK2):c.601C>A (p.Gln201Lys)	KANK2 (Q201K)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1615267	NM_001136191.3(KANK2):c.332A>G (p.Tyr111Cys)	KANK2 (Y111C)	Single nucleotide variant (missense variant)	KANK2-related disorder +1 more	GLikely benign
Select item 774524	NM_001136191.3(KANK2):c.10G>A (p.Val4Ile)	KANK2 (V4I)	Single nucleotide variant (missense variant)	KANK2-related disorder +3 more	GLikely benign

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Items: 31