Related gene-specific medical variations for Gene (Select 65010) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 64458	NM_022911.3(SLC26A6):c.709C>A (p.Leu237Ile)	SLC26A6 (L216I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 64457	NM_022911.3(SLC26A6):c.682G>C (p.Val228Leu)	SLC26A6 (V207L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 64456	NM_022911.3(SLC26A6):c.365G>A (p.Gly122Asp)	SLC26A6 (G101D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64455	NM_022911.3(SLC26A6):c.2081A>T (p.His694Leu)	SLC26A6 (H673L +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64454	NM_022911.3(SLC26A6):c.1902C>T (p.Ser634=)	SLC26A6	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 64453	NM_022911.3(SLC26A6):c.1653T>A (p.Phe551Leu)	SLC26A6 (F530L +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64452	NM_022911.3(SLC26A6):c.1631G>A (p.Arg544His)	SLC26A6 (R523H +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64451	NM_022911.3(SLC26A6):c.1618G>C (p.Val540Leu)	SLC26A6 (V519L +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 64450	NM_022911.3(SLC26A6):c.1566G>A (p.Thr522=)	SLC26A6	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 64449	NM_022911.3(SLC26A6):c.1541C>T (p.Ser514Phe)	SLC26A6 (S493F +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance