Related gene-specific medical variations for Gene (Select 254173) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329972	NM_001130045.2(TTLL10):c.40C>T (p.Pro14Ser)	TTLL10, TTLL10-AS1 (P14S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184533	NM_001130045.2(TTLL10):c.56G>A (p.Arg19Gln)	TTLL10, TTLL10-AS1 (R19Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2614396	NM_001130045.2(TTLL10):c.35G>C (p.Arg12Pro)	TTLL10, TTLL10-AS1 (R12P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487785	NM_001130045.2(TTLL10):c.71G>T (p.Arg24Met)	TTLL10, TTLL10-AS1 (R24M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393326	NM_001130045.2(TTLL10):c.49C>T (p.Arg17Trp)	TTLL10, TTLL10-AS1 (R17W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2306054	NM_001130045.2(TTLL10):c.53C>T (p.Thr18Ile)	TTLL10, TTLL10-AS1 (T18I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293894	NM_001130045.2(TTLL10):c.34C>T (p.Arg12Trp)	TTLL10, TTLL10-AS1 (R12W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293283	NM_001130045.2(TTLL10):c.110G>A (p.Arg37Gln)	TTLL10, TTLL10-AS1 (R37Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204057	NM_001130045.2(TTLL10):c.20G>A (p.Arg7Gln)	TTLL10, TTLL10-AS1 (R7Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance