FAM181A[gene] and "single gene"[properties] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3092079	NM_001207073.2(FAM181A):c.-57G>A	FAM181A (G44S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3092080	NM_001207073.2(FAM181A):c.-3G>C	FAM181A (V62L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3092081	NM_001207073.2(FAM181A):c.97C>T (p.Arg33Cys)	FAM181A (R33C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092082	NM_001207073.2(FAM181A):c.98G>A (p.Arg33His)	FAM181A (R33H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475512	NM_001207073.2(FAM181A):c.103G>A (p.Val35Met)	FAM181A (V97M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092083	NM_001207073.2(FAM181A):c.113G>A (p.Arg38His)	FAM181A (R100H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372641	NM_001207073.2(FAM181A):c.149A>G (p.Gln50Arg)	FAM181A (Q112R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539383	NM_001207073.2(FAM181A):c.160C>T (p.Arg54Trp)	FAM181A (R54W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340720	NM_001207073.2(FAM181A):c.196C>T (p.Pro66Ser)	FAM181A (P128S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353751	NM_001207073.2(FAM181A):c.280G>A (p.Gly94Ser)	FAM181A (G94S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462394	NM_001207073.2(FAM181A):c.285C>G (p.Cys95Trp)	FAM181A (C95W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258232	NM_001207073.2(FAM181A):c.308C>T (p.Pro103Leu)	FAM181A (P103L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395328	NM_001207073.2(FAM181A):c.463G>C (p.Gly155Arg)	FAM181A (G217R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092084	NM_001207073.2(FAM181A):c.506A>C (p.Lys169Thr)	FAM181A (K231T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092085	NM_001207073.2(FAM181A):c.583G>C (p.Glu195Gln)	FAM181A (E195Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092086	NM_001207073.2(FAM181A):c.587C>T (p.Pro196Leu)	FAM181A (P196L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244864	NM_001207073.2(FAM181A):c.601G>A (p.Gly201Arg)	FAM181A (G201R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357750	NM_001207073.2(FAM181A):c.613G>C (p.Val205Leu)	FAM181A (V267L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092088	NM_001207073.2(FAM181A):c.619C>T (p.Arg207Cys)	FAM181A (R269C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385414	NM_001207073.2(FAM181A):c.620G>A (p.Arg207His)	FAM181A (R269H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527338	NM_001207073.2(FAM181A):c.635G>A (p.Ser212Asn)	FAM181A (S212N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509283	NM_001207073.2(FAM181A):c.710C>A (p.Pro237His)	FAM181A (P237H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277280	NM_001207073.2(FAM181A):c.751G>A (p.Glu251Lys)	FAM181A (E251K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092090	NM_001207073.2(FAM181A):c.776T>C (p.Val259Ala)	FAM181A (V259A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 24