"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SLC9A9"[ge - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 788398	NM_173653.4(SLC9A9):c.1824C>T (p.Asp608=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1013232	NM_173653.4(SLC9A9):c.1808C>A (p.Ala603Glu)	SLC9A9 (A603E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2672962	NM_173653.4(SLC9A9):c.1719A>G (p.Leu573=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 789170	NM_173653.4(SLC9A9):c.1641G>A (p.Pro547=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2654207	NM_173653.4(SLC9A9):c.1390A>G (p.Thr464Ala)	SLC9A9 (T464A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 757091	NM_173653.4(SLC9A9):c.1158G>A (p.Thr386=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1176468	NM_173653.4(SLC9A9):c.846C>T (p.Phe282=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 757092	NM_173653.4(SLC9A9):c.759T>C (p.Ser253=)	SLC9A9	Single nucleotide variant (synonymous variant)	SLC9A9-related condition +1 more	GBenign/Likely benign
Select item 2578951	NM_173653.4(SLC9A9):c.723G>A (p.Val241=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3025096	NM_173653.4(SLC9A9):c.576C>A (p.Gly192=)	SLC9A9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1335541	NM_173653.4(SLC9A9):c.456+6T>C	SLC9A9	Single nucleotide variant (intron variant)	not provided	GLikely benign