"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC25A24" - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2631572	NM_013386.5(SLC25A24):c.1360G>A (p.Val454Met)	SLC25A24 (V435M +1 more)	Single nucleotide variant (missense variant)	SLC25A24-related condition	GUncertain significance
Select item 2717480	NM_013386.5(SLC25A24):c.823-10G>T	SLC25A24	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 3045648	NM_013386.5(SLC25A24):c.766A>G (p.Thr256Ala)	SLC25A24 (T237A +1 more)	Single nucleotide variant (missense variant)	SLC25A24-related condition	GUncertain significance
Select item 3042781	NM_013386.5(SLC25A24):c.669+6C>G	SLC25A24	Single nucleotide variant (intron variant)	SLC25A24-related condition	GLikely benign
Select item 3046208	NM_013386.5(SLC25A24):c.216T>C (p.Asp72=)	SLC25A24	Single nucleotide variant (synonymous variant)	SLC25A24-related condition	GLikely benign
Select item 3057627	NM_013386.5(SLC25A24):c.184-6576A>T	SLC25A24 (D31V)	Single nucleotide variant (missense variant +1 more)	SLC25A24-related condition	GBenign
Select item 1267873	NM_013386.5(SLC25A24):c.184-6636A>G	SLC25A24 (Y11C)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 1907765	NM_013386.5(SLC25A24):c.183+7C>T	SLC25A24	Single nucleotide variant (intron variant)	SLC25A24-related condition +1 more	GBenign/Likely benign
Select item 3057833	NM_013386.5(SLC25A24):c.75G>A (p.Glu25=)	SLC25A24	Single nucleotide variant (synonymous variant)	SLC25A24-related condition	GLikely benign
Select item 3034105	NM_013386.5(SLC25A24):c.60G>A (p.Gln20=)	SLC25A24	Single nucleotide variant (synonymous variant)	SLC25A24-related condition	GLikely benign