"Ambry Genetics"[submitter] AND "CD200R1L"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2482738	NM_001199215.3(CD200R1L):c.734A>G (p.His245Arg)	CD200R1L, CD200R1L-AS1 (H245R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2594172	NM_001199215.3(CD200R1L):c.685G>A (p.Val229Met)	CD200R1L, CD200R1L-AS1 (V250M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2241029	NM_001199215.3(CD200R1L):c.683T>C (p.Phe228Ser)	CD200R1L, CD200R1L-AS1 (F228S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3140425	NM_001199215.3(CD200R1L):c.679C>G (p.Leu227Val)	CD200R1L, CD200R1L-AS1 (L248V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2219335	NM_001199215.3(CD200R1L):c.635C>G (p.Ser212Cys)	CD200R1L, CD200R1L-AS1 (S212C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2297786	NM_001199215.3(CD200R1L):c.623G>A (p.Arg208Lys)	CD200R1L, CD200R1L-AS1 (R229K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2293941	NM_001199215.3(CD200R1L):c.619C>T (p.Leu207Phe)	CD200R1L, CD200R1L-AS1 (L207F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3140424	NM_001199215.3(CD200R1L):c.601G>A (p.Val201Ile)	CD200R1L (V201I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140423	NM_001199215.3(CD200R1L):c.580A>T (p.Thr194Ser)	CD200R1L (T194S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326404	NM_001199215.3(CD200R1L):c.579G>C (p.Leu193Phe)	CD200R1L (L214F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513782	NM_001199215.3(CD200R1L):c.554C>T (p.Thr185Ile)	CD200R1L (T185I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524416	NM_001199215.3(CD200R1L):c.542G>T (p.Gly181Val)	CD200R1L (G181V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140422	NM_001199215.3(CD200R1L):c.421G>A (p.Ala141Thr)	CD200R1L (A141T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467376	NM_001199215.3(CD200R1L):c.343C>T (p.Arg115Cys)	CD200R1L (R115C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279417	NM_001199215.3(CD200R1L):c.338T>G (p.Phe113Cys)	CD200R1L (F134C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314491	NM_001199215.3(CD200R1L):c.299G>A (p.Gly100Glu)	CD200R1L (G100E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140421	NM_001199215.3(CD200R1L):c.287C>T (p.Thr96Ile)	CD200R1L (T117I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2238317	NM_001199215.3(CD200R1L):c.262G>C (p.Asp88His)	CD200R1L (D88H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140420	NM_001199215.3(CD200R1L):c.179A>G (p.Tyr60Cys)	CD200R1L (Y60C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203932	NM_001199215.3(CD200R1L):c.109G>A (p.Ala37Thr)	CD200R1L (A37T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528038	NM_001199215.3(CD200R1L):c.107T>C (p.Ile36Thr)	CD200R1L (I57T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140419	NM_001199215.3(CD200R1L):c.88G>A (p.Val30Met)	CD200R1L (V30M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22