"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "TRIM37"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1431491	NM_015294.6(TRIM37):c.2707G>A (p.Asp903Asn)	LOC126862606, TRIM37 (D903N +6 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1336449	NM_015294.6(TRIM37):c.2600T>C (p.Leu867Pro)	TRIM37 (L622P +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 285792	NM_015294.6(TRIM37):c.2240A>G (p.Asn747Ser)	TRIM37 (N747S +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 559040	NM_015294.6(TRIM37):c.2229A>G (p.Ser743=)	TRIM37	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 559041	NM_015294.6(TRIM37):c.2169A>G (p.Ala723=)	TRIM37	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 559042	NM_015294.6(TRIM37):c.2136C>T (p.Ser712=)	TRIM37	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2186486	NM_015294.6(TRIM37):c.1189G>A (p.Val397Met)	TRIM37 (V397M +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 324206	NM_015294.6(TRIM37):c.810-13dup	TRIM37	Duplication (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 324207	NM_015294.6(TRIM37):c.810-3del	TRIM37	Deletion (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 5240	NM_015294.6(TRIM37):c.493-2A>G	TRIM37	Single nucleotide variant (splice acceptor variant)	not provided +1 more	GPathogenic
Select item 2366962	NM_015294.6(TRIM37):c.296A>G (p.His99Arg)	TRIM37 (H99R +1 more)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases +2 more	GUncertain significance