"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC26A8"[ - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 730861	NM_052961.4(SLC26A8):c.2894A>G (p.Asn965Ser)	SLC26A8 (N860S +1 more)	Single nucleotide variant (missense variant)	SLC26A8-related disorder +1 more	GLikely benign
Select item 3033960	NM_052961.4(SLC26A8):c.2613G>C (p.Gly871=)	SLC26A8	Single nucleotide variant (synonymous variant)	SLC26A8-related disorder	GLikely benign
Select item 3044807	NM_052961.4(SLC26A8):c.2200G>A (p.Val734Met)	SLC26A8 (V629M +1 more)	Single nucleotide variant (missense variant)	SLC26A8-related disorder	GLikely benign
Select item 711975	NM_052961.4(SLC26A8):c.1492A>G (p.Ile498Val)	SLC26A8 (I393V +1 more)	Single nucleotide variant (missense variant)	SLC26A8-related disorder +1 more	GBenign/Likely benign
Select item 3042448	NM_052961.4(SLC26A8):c.837C>A (p.Thr279=)	SLC26A8	Single nucleotide variant (synonymous variant +1 more)	SLC26A8-related disorder	GLikely benign
Select item 3043287	NM_052961.4(SLC26A8):c.643T>C (p.Leu215=)	SLC26A8	Single nucleotide variant (synonymous variant +1 more)	SLC26A8-related disorder	GLikely benign
Select item 3038455	NM_052961.4(SLC26A8):c.639C>T (p.Gly213=)	SLC26A8	Single nucleotide variant (synonymous variant +1 more)	SLC26A8-related disorder	GLikely benign
Select item 2656512	NM_052961.4(SLC26A8):c.378C>T (p.Ile126=)	SLC26A8	Single nucleotide variant (synonymous variant)	SLC26A8-related disorder +1 more	GLikely benign
Select item 3037302	NM_052961.4(SLC26A8):c.285C>T (p.Asp95=)	SLC26A8	Single nucleotide variant (synonymous variant)	SLC26A8-related disorder	GLikely benign