ARFRP1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2511312	NM_001267547.3(ARFRP1):c.587G>A (p.Arg196Gln)	ARFRP1 (R196Q +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2536046	NM_001267547.3(ARFRP1):c.581C>T (p.Pro194Leu)	ARFRP1 (P147L +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2554862	NM_001267547.3(ARFRP1):c.554A>G (p.Lys185Arg)	ARFRP1 (K185R +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2458630	NM_001267547.3(ARFRP1):c.526G>T (p.Val176Leu)	ARFRP1 (V129L +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3128431	NM_001267547.3(ARFRP1):c.482G>A (p.Arg161Gln)	ARFRP1 (R114Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 781505	NM_001267547.3(ARFRP1):c.447G>A (p.Thr149=)	ARFRP1	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2324002	NM_001267547.3(ARFRP1):c.446C>T (p.Thr149Met)	ARFRP1 (T102M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2227441	NM_001267547.3(ARFRP1):c.419C>T (p.Thr140Met)	ARFRP1 (T140M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2314488	NM_001267547.3(ARFRP1):c.407A>G (p.Gln136Arg)	ARFRP1 (Q89R +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2321476	NM_001267547.3(ARFRP1):c.374G>A (p.Cys125Tyr)	ARFRP1 (C78Y +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2214471	NM_001267547.3(ARFRP1):c.368C>T (p.Ala123Val)	ARFRP1 (A123V +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2535515	NM_001267547.3(ARFRP1):c.334A>G (p.Lys112Glu)	ARFRP1 (K65E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128429	NM_001267547.3(ARFRP1):c.238G>A (p.Glu80Lys)	ARFRP1 (E33K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128428	NM_001267547.3(ARFRP1):c.211C>G (p.Leu71Val)	ARFRP1 (L71V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376746	NM_001267547.3(ARFRP1):c.136A>G (p.Lys46Glu)	ARFRP1 (K46E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance