"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "RNF31"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3005521	NM_017999.5(RNF31):c.114A>T (p.Leu38=)	RNF31	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1169281	NM_017999.5(RNF31):c.415G>A (p.Glu139Lys)	RNF31 (E139K)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1120437	NM_017999.5(RNF31):c.431A>C (p.His144Pro)	RNF31 (H144P)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1611588	NM_017999.5(RNF31):c.543G>A (p.Lys181=)	RNF31	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2644130	NM_017999.5(RNF31):c.729G>A (p.Leu243=)	RNF31	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1602502	NM_017999.5(RNF31):c.1590C>T (p.Tyr530=)	RNF31	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1128470	NM_017999.5(RNF31):c.1865A>T (p.Gln622Leu)	RNF31 (Q471L +1 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1566460	NM_017999.5(RNF31):c.2358C>T (p.Thr786=)	RNF31	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1608305	NM_017999.5(RNF31):c.2631G>A (p.Ser877=)	RNF31	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1166489	NM_017999.5(RNF31):c.2928G>A (p.Glu976=)	RNF31	Single nucleotide variant (synonymous variant)	RNF31-related condition +1 more	GBenign/Likely benign