"Illumina Laboratory Services, Illumina"[submitter] AND "NRAP"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 879493	NM_198060.4(NRAP):c.*257G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 879494	NM_198060.4(NRAP):c.*246T>G	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298926	NM_198060.4(NRAP):c.*241T>C	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GLikely benign
Select item 298927	NM_198060.4(NRAP):c.*188G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298928	NM_198060.4(NRAP):c.*139G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298929	NM_198060.4(NRAP):c.*79G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 879852	NM_198060.4(NRAP):c.*41T>C	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia	GLikely benign
Select item 298930	NM_198060.4(NRAP):c.*7del	HABP2, NRAP	Deletion (3 prime UTR variant)	Factor VII Marburg I Variant Thrombophilia +1 more	GBenign/Likely benign
Select item 298931	NM_198060.4(NRAP):c.5170AAG[2] (p.Lys1726del)	HABP2, NRAP (K1690del +3 more)	Microsatellite (3 prime UTR variant +1 more)	NRAP-related condition +2 more	GBenign/Likely benign
Select item 298932	NM_198060.4(NRAP):c.5155A>C (p.Ile1719Leu)	HABP2, NRAP (I1683L +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298933	NM_198060.4(NRAP):c.5117A>C (p.Asp1706Ala)	HABP2, NRAP (D1706A +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298934	NM_198060.4(NRAP):c.5089-55G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298935	NM_198060.4(NRAP):c.5089-78C>T	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia +1 more	GBenign
Select item 877911	NM_198060.4(NRAP):c.5089-92C>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 877912	NM_198060.4(NRAP):c.5089-103G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 877913	NM_198060.4(NRAP):c.5089-112G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298936	NM_198060.4(NRAP):c.5089-113G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298937	NM_198060.4(NRAP):c.5089-149T>C	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298938	NM_198060.4(NRAP):c.5089-159A>C	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GLikely benign
Select item 298939	NM_198060.4(NRAP):c.5089-209A>C	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298940	NM_198060.4(NRAP):c.5088+258A>G	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298941	NM_198060.4(NRAP):c.5088+246G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298942	NM_198060.4(NRAP):c.5088+245C>T	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298943	NM_198060.4(NRAP):c.5088+209A>G	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298944	NM_198060.4(NRAP):c.5088+182G>T	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GLikely benign
Select item 878080	NM_198060.4(NRAP):c.5088+173G>T	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298945	NM_198060.4(NRAP):c.5088+138G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance
Select item 298946	NM_198060.4(NRAP):c.5088+137C>T	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GBenign
Select item 879537	NM_198060.4(NRAP):c.5088+122G>A	HABP2, NRAP	Single nucleotide variant (3 prime UTR variant +1 more)	Factor VII Marburg I Variant Thrombophilia	GUncertain significance

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Items: 29