ClinVar for Gene (Select 4067) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3351878	NM_002350.4(LYN):c.317T>C (p.Leu106Ser)	LYN (L106S +1 more)	Single nucleotide variant (missense variant)	LYN-related disorder	GUncertain significance
Select item 3292374	NM_002350.4(LYN):c.919G>A (p.Ala307Thr)	LYN (A286T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3257922	NM_002350.4(LYN):c.1229C>T (p.Thr410Met)	LYN (T389M +1 more)	Single nucleotide variant (missense variant)	Neoplasm	OUncertain significance
Select item 3121670	NM_002350.4(LYN):c.934G>A (p.Glu312Lys)	LYN (E291K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3065788	NM_002350.4(LYN):c.488G>T (p.Gly163Val)	LYN (G142V +1 more)	Single nucleotide variant (missense variant)	Autoinflammatory disease, systemic, with vasculitis	GUncertain significance
Select item 3063025	GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	PREX2, PRKDC +240 more	Copy number gain	not specified	GPathogenic
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 3010986	NM_002350.4(LYN):c.488-9C>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3008199	NM_002350.4(LYN):c.1392T>C (p.Arg464=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005363	NM_002350.4(LYN):c.612C>T (p.Ile204=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2985565	NM_002350.4(LYN):c.886A>G (p.Thr296Ala)	LYN (T275A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2984197	NM_002350.4(LYN):c.1337-10dup	LYN	Duplication (intron variant)	not provided	GBenign
Select item 2981674	NM_002350.4(LYN):c.284+8CT[4]	LYN	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2979741	NM_002350.4(LYN):c.488-11T>G	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977587	NM_002350.4(LYN):c.1129G>A (p.Glu377Lys)	LYN (E356K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2973487	NM_002350.4(LYN):c.133-14A>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973159	NM_002350.4(LYN):c.687C>G (p.Pro229=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2971586	NM_002350.4(LYN):c.1336+18A>G	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969982	NM_002350.4(LYN):c.234C>T (p.His78=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2969082	NM_002350.4(LYN):c.1204+8G>A	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2968460	NM_002350.4(LYN):c.122A>G (p.Gln41Arg)	LYN (Q41R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2964008	NM_002350.4(LYN):c.132+13T>A	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961827	NM_002350.4(LYN):c.475G>A (p.Glu159Lys)	LYN (E159K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2959890	NM_002350.4(LYN):c.1485C>T (p.Ser495=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957727	NM_002350.4(LYN):c.248C>G (p.Ser83Cys)	LYN (S83C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2918671	NM_002350.4(LYN):c.111G>A (p.Thr37=)	LYN	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2914791	NM_002350.4(LYN):c.906C>T (p.Leu302=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2911677	NM_002350.4(LYN):c.1079G>A (p.Arg360Gln)	LYN (R339Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2909008	NM_002350.4(LYN):c.184G>A (p.Glu62Lys)	LYN (E62K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2905761	NM_002350.4(LYN):c.480A>G (p.Thr160=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2902960	NM_002350.4(LYN):c.377C>T (p.Thr126Ile)	LYN (T126I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902439	NM_002350.4(LYN):c.284+9T>C	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2899694	NM_002350.4(LYN):c.791-9_791-8delinsAA	LYN	Indel (intron variant)	not provided	GUncertain significance
Select item 2899134	NM_002350.4(LYN):c.133-5C>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2892013	NM_002350.4(LYN):c.133G>A (p.Val45Ile)	LYN (V24I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2857871	NM_002350.4(LYN):c.1247A>C (p.Asn416Thr)	LYN (N395T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2853373	NM_002350.4(LYN):c.178+13A>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2844119	NM_002350.4(LYN):c.790+5dup	LYN	Duplication (intron variant)	not provided	GUncertain significance
Select item 2835716	NM_002350.4(LYN):c.810C>G (p.Thr270=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2835513	NM_002350.4(LYN):c.36G>A (p.Leu12=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2829659	NM_002350.4(LYN):c.1337-16T>G	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2826559	NM_002350.4(LYN):c.1349C>G (p.Ala450Gly)	LYN (A429G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2814163	NM_002350.4(LYN):c.1204+5G>A	LYN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2813559	NM_002350.4(LYN):c.1107A>G (p.Arg369=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2808951	NM_002350.4(LYN):c.1212G>A (p.Lys404=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2801463	NM_002350.4(LYN):c.1051-20G>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2799522	NM_002350.4(LYN):c.23G>A (p.Gly8Glu)	LYN (G8E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2786240	NM_002350.4(LYN):c.217C>G (p.Pro73Ala)	LYN (P52A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2784649	NM_002350.4(LYN):c.570T>C (p.Asn190=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2776154	NM_002350.4(LYN):c.487+14C>A	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2765419	NM_002350.4(LYN):c.151T>C (p.Leu51=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2759189	NM_002350.4(LYN):c.240C>T (p.Asp80=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2758988	NM_002350.4(LYN):c.608G>T (p.Cys203Phe)	LYN (C182F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2751471	NM_002350.4(LYN):c.285-19A>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2746051	NM_002350.4(LYN):c.438A>C (p.Pro146=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2719841	NM_002350.4(LYN):c.273A>G (p.Lys91=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2708603	NM_002350.4(LYN):c.132+17_132+18del	LYN	Deletion (intron variant)	not provided	GLikely benign
Select item 2706482	NM_002350.4(LYN):c.1185T>C (p.Asn395=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2695370	NM_002350.4(LYN):c.243C>T (p.Asp81=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2695345	NM_002350.4(LYN):c.417A>G (p.Ala139=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2502324	NM_002350.4(LYN):c.1522T>C (p.Tyr508His)	LYN (Y487H)	Single nucleotide variant (missense variant)	Autoinflammatory disease, systemic, with vasculitis	GPathogenic
Select item 2424417	NC_000008.10:g.(?_56854419)_(56882372_?)dup	LYN	Duplication	not provided	GUncertain significance
Select item 2417831	NM_002350.4(LYN):c.448G>T (p.Ala150Ser)	LYN (A129S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2416764	NM_002350.4(LYN):c.1029G>A (p.Lys343=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2416414	NM_002350.4(LYN):c.918C>T (p.Tyr306=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2414873	NM_002350.4(LYN):c.974-3T>C	LYN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2282372	NM_002350.4(LYN):c.1079G>T (p.Arg360Leu)	LYN (R360L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2190250	NM_002350.4(LYN):c.790+10C>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2187174	NM_002350.4(LYN):c.10A>G (p.Ile4Val)	LYN (I4V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2186710	NM_002350.4(LYN):c.314T>C (p.Leu105Pro)	LYN (L105P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2180907	NM_002350.4(LYN):c.604C>G (p.Pro202Ala)	LYN (P202A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2177577	NM_002350.4(LYN):c.133-4G>A	LYN	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 2170100	NM_002350.4(LYN):c.1230G>A (p.Thr410=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2151302	NM_002350.4(LYN):c.726C>T (p.Ile242=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2136672	NM_002350.4(LYN):c.359A>T (p.Lys120Ile)	LYN (K99I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2126942	NM_002350.4(LYN):c.284+7G>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2126407	NM_002350.4(LYN):c.284+12C>G	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2118063	NM_002350.4(LYN):c.264G>T (p.Glu88Asp)	LYN (E88D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2114851	NM_002350.4(LYN):c.579T>C (p.Tyr193=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2111367	NM_002350.4(LYN):c.156T>A (p.Pro52=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2104344	NM_002350.4(LYN):c.957C>A (p.Thr319=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2098405	NM_002350.4(LYN):c.1096C>T (p.Arg366Trp)	LYN (R345W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2096662	NM_002350.4(LYN):c.505G>C (p.Val169Leu)	LYN (V169L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2094712	NM_002350.4(LYN):c.818C>T (p.Ala273Val)	LYN (A252V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2094361	NM_002350.4(LYN):c.178+12T>C	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2086584	NM_002350.4(LYN):c.978T>C (p.Ser326=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2073194	NM_002350.4(LYN):c.998G>A (p.Ser333Asn)	LYN (S312N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2072684	NM_002350.4(LYN):c.179-8A>C	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2072617	NM_002350.4(LYN):c.1302C>T (p.Tyr434=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2057512	NM_002350.4(LYN):c.643G>A (p.Ala215Thr)	LYN (A194T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2051837	NM_002350.4(LYN):c.179-4T>C	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2051279	NM_002350.4(LYN):c.1050+8_1050+9del	LYN	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2050883	NM_002350.4(LYN):c.141A>G (p.Glu47=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2047874	NM_002350.4(LYN):c.1336+16C>T	LYN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2034412	NM_002350.4(LYN):c.72A>G (p.Val24=)	LYN	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2016815	NM_002350.4(LYN):c.398A>G (p.Asp133Gly)	LYN (D112G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2008756	NM_002350.4(LYN):c.488-18_488-17insAA	LYN	Insertion (intron variant)	not provided	GLikely benign
Select item 2003945	NM_002350.4(LYN):c.599C>G (p.Thr200Ser)	LYN (T179S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1978787	NM_002350.4(LYN):c.1515A>G (p.Glu505=)	LYN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1976380	NM_002350.4(LYN):c.604C>T (p.Pro202Ser)	LYN (P181S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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