"PreventionGenetics, part of Exact Sciences"[submitter] AND "CR1"[gene - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 17066	NM_000651.6(CR1):c.4973A>G (p.His1658Arg)	CR1 (H1658R)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 3047970	NM_000651.6(CR1):c.5302C>T (p.His1768Tyr)	CR1 (H1318Y +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 3038909	NM_000651.6(CR1):c.5572A>G (p.Thr1858Ala)	CR1 (T1408A +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 3052016	NM_000651.6(CR1):c.5605G>A (p.Gly1869Arg)	CR1 (G1419R +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GLikely benign
Select item 3056664	NM_000651.6(CR1):c.5969A>G (p.Asn1990Ser)	CR1 (N1540S +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 3051184	NM_000651.6(CR1):c.6096C>T (p.Pro2032=)	CR1	Single nucleotide variant (synonymous variant)	CR1-related condition	GLikely benign
Select item 3056450	NM_000651.6(CR1):c.6118A>G (p.Lys2040Glu)	CR1 (K1590E +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 3056679	NM_000651.6(CR1):c.6151A>G (p.Arg2051Gly)	CR1 (R1601G +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 1252113	NM_000651.6(CR1):c.6193A>G (p.Ile2065Val)	CR1 (I2065V +1 more)	Single nucleotide variant (missense variant)	CR1-related condition +1 more	GBenign
Select item 3059361	NM_000651.6(CR1):c.6830C>G (p.Pro2277Arg)	CR1 (P1827R +1 more)	Single nucleotide variant (missense variant)	CR1-related condition	GBenign
Select item 3024752	NM_000651.6(CR1):c.6908A>G (p.Lys2303Arg)	CR1 (K1853R +1 more)	Single nucleotide variant (missense variant)	CR1-related condition +1 more	GBenign