Related gene-specific medical variations for Gene (Select 245711) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3183092	NM_017910.4(TRMT61B):c.1403A>C (p.Lys468Thr)	SPDYA, TRMT61B (K468T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3183091	NM_017910.4(TRMT61B):c.1381G>C (p.Gly461Arg)	SPDYA, TRMT61B (G461R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2480747	NM_017910.4(TRMT61B):c.1400T>C (p.Val467Ala)	SPDYA, TRMT61B (V467A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2403423	NM_017910.4(TRMT61B):c.1362A>C (p.Arg454Ser)	SPDYA, TRMT61B (R454S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2250248	NM_182756.4(SPDYA):c.862C>T (p.His288Tyr)	SPDYA, TRMT61B (H288Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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