Related gene-specific medical variations for Gene (Select 5902) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329083	NM_022727.6(TRMT2A):c.508G>A (p.Asp170Asn)	RANBP1, TRMT2A (D170N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183048	NM_022727.6(TRMT2A):c.434G>A (p.Arg145Gln)	RANBP1, TRMT2A (R145Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183047	NM_022727.6(TRMT2A):c.296A>T (p.Gln99Leu)	RANBP1, TRMT2A (C53S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183046	NM_022727.6(TRMT2A):c.254G>C (p.Ser85Thr)	RANBP1, TRMT2A (L67V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183045	NM_022727.6(TRMT2A):c.206C>G (p.Thr69Ser)	RANBP1, TRMT2A (T69S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3183043	NM_022727.6(TRMT2A):c.175C>G (p.Leu59Val)	RANBP1, TRMT2A (L59V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652882	NM_001278639.2(RANBP1):c.243A>C (p.Ser81=)	RANBP1, TRMT2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2652881	NM_022727.6(TRMT2A):c.339T>C (p.Phe113=)	RANBP1, TRMT2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2560888	NM_022727.6(TRMT2A):c.44G>A (p.Ser15Asn)	RANBP1, TRMT2A (S15N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459043	NM_022727.6(TRMT2A):c.515T>C (p.Val172Ala)	RANBP1, TRMT2A (V172A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400730	NM_022727.6(TRMT2A):c.488C>T (p.Pro163Leu)	RANBP1, TRMT2A (P163L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389220	NM_022727.6(TRMT2A):c.317T>C (p.Phe106Ser)	RANBP1, TRMT2A (K46E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365820	NM_022727.6(TRMT2A):c.382G>A (p.Val128Ile)	RANBP1, TRMT2A (T24M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358653	NM_022727.6(TRMT2A):c.334G>A (p.Ala112Thr)	RANBP1, TRMT2A (A112T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346878	NM_022727.6(TRMT2A):c.284G>A (p.Arg95His)	RANBP1, TRMT2A (R57W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329523	NM_022727.6(TRMT2A):c.380G>T (p.Arg127Leu)	RANBP1, TRMT2A (R25S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257580	NM_022727.6(TRMT2A):c.524T>C (p.Leu175Pro)	RANBP1, TRMT2A (L175P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance