Related gene-specific medical variations for Gene (Select 162515) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3318915	NM_001370549.1(SLC16A11):c.881T>C (p.Leu294Pro)	LOC130060102, SLC16A11 (L294P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163067	NM_001370549.1(SLC16A11):c.761G>A (p.Gly254Glu)	LOC130060102, SLC16A11 (G254E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163065	NM_001370549.1(SLC16A11):c.586C>A (p.Pro196Thr)	LOC130060102, SLC16A11 (P196T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543804	NM_001370549.1(SLC16A11):c.680C>G (p.Thr227Arg)	LOC130060102, SLC16A11 (T227R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471813	NM_001370549.1(SLC16A11):c.716T>C (p.Val239Ala)	LOC130060102, SLC16A11 (V239A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460331	NM_001370549.1(SLC16A11):c.1088G>A (p.Gly363Glu)	LOC130060101, SLC16A11 (G363E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349439	NM_001370549.1(SLC16A11):c.641T>C (p.Leu214Pro)	LOC130060102, SLC16A11 (L214P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348149	NM_001370549.1(SLC16A11):c.610C>T (p.Arg204Cys)	LOC130060102, SLC16A11 (R204C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311561	NM_001370549.1(SLC16A11):c.760G>A (p.Gly254Arg)	LOC130060102, SLC16A11 (G254R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270902	NM_001370549.1(SLC16A11):c.904G>A (p.Val302Met)	LOC130060102, SLC16A11 (V302M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266898	NM_001370549.1(SLC16A11):c.683C>G (p.Ala228Gly)	LOC130060102, SLC16A11 (A228G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257972	NM_001370549.1(SLC16A11):c.697G>A (p.Gly233Arg)	LOC130060102, SLC16A11 (G233R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226065	NM_001370549.1(SLC16A11):c.709C>T (p.Pro237Ser)	LOC130060102, SLC16A11 (P237S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223938	NM_001370549.1(SLC16A11):c.752G>C (p.Gly251Ala)	LOC130060102, SLC16A11 (G251A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance