Related gene-specific medical variations for Gene (Select 29887) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3013051	NM_013322.3(SNX10):c.525-4C>T	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2964029	NM_013322.3(SNX10):c.525-16CT[2]	SNX10-AS1, SNX10	Microsatellite (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2750143	NM_013322.3(SNX10):c.525-20C>A	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2699294	NM_013322.3(SNX10):c.525-14C>T	SNX10, SNX10-AS1	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2476340	NM_013322.3(SNX10):c.566C>T (p.Ser189Leu)	SNX10, SNX10-AS1 (S186L +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2271991	NM_013322.3(SNX10):c.602C>T (p.Ser201Phe)	SNX10, SNX10-AS1 (S201F +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2124250	NM_013322.3(SNX10):c.531C>G (p.Ser177=)	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2058198	NM_013322.3(SNX10):c.525-20C>T	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1992125	NM_013322.3(SNX10):c.525-4C>G	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1927555	NM_013322.3(SNX10):c.524+11G>A	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1661383	NM_013322.3(SNX10):c.525-16del	SNX10, SNX10-AS1	Deletion (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1573480	NM_013322.3(SNX10):c.537G>A (p.Gly179=)	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	SNX10-related disorder +1 more	GBenign/Likely benign
Select item 1505826	NM_013322.3(SNX10):c.593C>T (p.Pro198Leu)	SNX10, SNX10-AS1 (P195L +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1464340	NM_013322.3(SNX10):c.529T>C (p.Ser177Pro)	SNX10, SNX10-AS1 (S203P +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1373756	NM_013322.3(SNX10):c.524+1G>T	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1355371	NM_013322.3(SNX10):c.535G>T (p.Gly179Trp)	SNX10, SNX10-AS1 (G179W +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 735305	NM_013322.3(SNX10):c.531C>T (p.Ser177=)	SNX10, SNX10-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 685615	GRCh37/hg19 7p15.2(chr7:26276080-26407744)x3	SNX10	Copy number gain	not provided	GUncertain significance