Related gene-specific medical variations for Gene (Select 22955) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3316483	NM_001394311.1(SCMH1):c.1793G>A (p.Arg598Gln)	SCMH1, SLFNL1-AS1 (R408Q +12 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3158470	NM_001394311.1(SCMH1):c.1991G>A (p.Arg664Gln)	SCMH1, SLFNL1-AS1 (R654Q +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158469	NM_001394311.1(SCMH1):c.1769G>T (p.Arg590Leu)	SCMH1, SLFNL1-AS1 (R412L +12 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3158468	NM_001394311.1(SCMH1):c.1764G>T (p.Glu588Asp)	SCMH1, SLFNL1-AS1 (E398D +12 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3158467	NM_001394311.1(SCMH1):c.1643G>A (p.Ser548Asn)	SCMH1, SLFNL1-AS1 (S380N +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158466	NM_001394311.1(SCMH1):c.1613C>T (p.Pro538Leu)	SCMH1, SLFNL1-AS1 (P481L +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2638727	NM_001394311.1(SCMH1):c.1668A>G (p.Leu556=)	SCMH1, SLFNL1-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2481052	NM_001394311.1(SCMH1):c.1628G>A (p.Cys543Tyr)	SCMH1, SLFNL1-AS1 (C486Y +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373461	NM_001394311.1(SCMH1):c.1889A>G (p.Glu630Gly)	SCMH1, SLFNL1-AS1 (E510G +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257715	NM_001394311.1(SCMH1):c.1499G>T (p.Gly500Val)	SCMH1, SLFNL1-AS1 (G399V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219445	NM_001394311.1(SCMH1):c.1751A>G (p.Asp584Gly)	SCMH1, SLFNL1-AS1 (D464G +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212701	NM_001394311.1(SCMH1):c.1558A>G (p.Met520Val)	SCMH1, SLFNL1-AS1 (M342V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212687	NM_001394311.1(SCMH1):c.1531C>T (p.Arg511Cys)	SCMH1, SLFNL1-AS1 (R501C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance