"Ambry Genetics"[submitter] AND "FAR2"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2320779	NM_001271783.2(FAR2):c.28G>A (p.Gly10Ser)	FAR2 (G10S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092862	NM_001271783.2(FAR2):c.130G>A (p.Val44Met)	FAR2 (V44M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092863	NM_001271783.2(FAR2):c.136C>A (p.Pro46Thr)	FAR2 (P46T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607157	NM_001271783.2(FAR2):c.139A>G (p.Lys47Glu)	FAR2 (K47E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321645	NM_001271783.2(FAR2):c.166G>A (p.Val56Ile)	FAR2 (V56I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393998	NM_001271783.2(FAR2):c.196G>C (p.Glu66Gln)	FAR2, LOC100506606 (E66Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2410946	NM_001271783.2(FAR2):c.206A>G (p.Lys69Arg)	FAR2, LOC100506606 (K69R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2539661	NM_001271783.2(FAR2):c.211G>A (p.Val71Ile)	FAR2, LOC100506606 (V71I)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2275370	NM_001271783.2(FAR2):c.292A>T (p.Met98Leu)	FAR2, LOC100506606 (M98L +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2595948	NM_001271783.2(FAR2):c.409C>G (p.Leu137Val)	FAR2, LOC100506606 (L40V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300245	NM_001271783.2(FAR2):c.620C>G (p.Thr207Ser)	FAR2, LOC100506606 (T110S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220584	NM_001271783.2(FAR2):c.795A>G (p.Ile265Met)	FAR2, LOC100506606 (I265M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569099	NM_001271783.2(FAR2):c.844G>A (p.Val282Ile)	FAR2, LOC100506606 (V185I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602138	NM_001271783.2(FAR2):c.847A>G (p.Asn283Asp)	FAR2, LOC100506606 (N186D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297920	NM_001271783.2(FAR2):c.893A>T (p.Lys298Met)	FAR2, LOC100506606 (K298M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270313	NM_001271783.2(FAR2):c.973A>G (p.Thr325Ala)	FAR2, LOC100506606 (T228A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092860	NM_001271783.2(FAR2):c.1073G>A (p.Arg358Gln)	FAR2, LOC100506606 (R358Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371049	NM_001271783.2(FAR2):c.1168A>G (p.Met390Val)	FAR2 (M390V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092861	NM_001271783.2(FAR2):c.1190G>A (p.Arg397Gln)	FAR2 (R300Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389690	NM_001271783.2(FAR2):c.1208C>T (p.Thr403Met)	FAR2 (T403M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316999	NM_001271783.2(FAR2):c.1256G>A (p.Arg419Lys)	FAR2 (R322K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496116	NM_001271783.2(FAR2):c.1351G>T (p.Ala451Ser)	FAR2 (A354S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554757	NM_001271783.2(FAR2):c.1468C>G (p.Arg490Gly)	FAR2 (R490G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092864	NM_001271783.2(FAR2):c.1523G>C (p.Arg508Thr)	FAR2 (R411T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 24