Related gene-specific medical variations for Gene (Select 54509) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3154082	NM_019034.3(RHOF):c.583G>A (p.Ala195Thr)	RHOF, TMEM120B (A195T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3154080	NM_019034.3(RHOF):c.365G>A (p.Arg122His)	TMEM120B, RHOF (R122H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3154079	NM_019034.3(RHOF):c.245G>A (p.Arg82Gln)	RHOF, TMEM120B (R82Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3154078	NM_019034.3(RHOF):c.185T>C (p.Val62Ala)	RHOF, SETD1B (V62A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643414	NM_019034.3(RHOF):c.372C>A (p.Ile124=)	RHOF, TMEM120B	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2455213	NM_019034.3(RHOF):c.106C>T (p.Leu36Phe)	RHOF, SETD1B (L36F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366432	NM_019034.3(RHOF):c.601C>T (p.Arg201Trp)	RHOF, TMEM120B (R201W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2328803	NM_019034.3(RHOF):c.198G>T (p.Glu66Asp)	RHOF, SETD1B (E66D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267262	NM_019034.3(RHOF):c.487G>A (p.Glu163Lys)	RHOF, TMEM120B (E163K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2263462	NM_019034.3(RHOF):c.458T>C (p.Ile153Thr)	RHOF, TMEM120B (I153T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2244252	NM_019034.3(RHOF):c.203C>T (p.Thr68Ile)	RHOF, SETD1B (T68I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242021	NM_019034.3(RHOF):c.437G>A (p.Arg146Gln)	RHOF, TMEM120B (R146Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance