SLC16A10[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3318908	NM_018593.5(SLC16A10):c.176A>G (p.His59Arg)	SLC16A10 (H59R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318909	NM_018593.5(SLC16A10):c.194C>T (p.Pro65Leu)	SLC16A10 (P65L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494327	NM_018593.5(SLC16A10):c.248C>T (p.Ser83Leu)	SLC16A10 (S83L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 737124	NM_018593.5(SLC16A10):c.252G>A (p.Val84=)	SLC16A10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2475366	NM_018593.5(SLC16A10):c.314A>G (p.Lys105Arg)	SLC16A10 (K105R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568889	NM_018593.5(SLC16A10):c.316G>A (p.Asp106Asn)	SLC16A10 (D106N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288342	NM_018593.5(SLC16A10):c.328A>T (p.Met110Leu)	SLC16A10 (M110L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409042	NM_018593.5(SLC16A10):c.425G>A (p.Arg142Gln)	SLC16A10 (R142Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524779	NM_018593.5(SLC16A10):c.437T>C (p.Val146Ala)	SLC16A10 (V146A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555628	NM_018593.5(SLC16A10):c.451G>C (p.Val151Leu)	SLC16A10 (V151L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713154	NM_018593.5(SLC16A10):c.562T>C (p.Leu188=)	SLC16A10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3163055	NM_018593.5(SLC16A10):c.579C>G (p.His193Gln)	SLC16A10 (H193Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606893	NM_018593.5(SLC16A10):c.644T>A (p.Ile215Asn)	SLC16A10 (I215N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782253	NM_018593.5(SLC16A10):c.738G>C (p.Leu246=)	SLC16A10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3163056	NM_018593.5(SLC16A10):c.799G>A (p.Gly267Arg)	SLC16A10 (G267R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3163057	NM_018593.5(SLC16A10):c.808C>T (p.Leu270Phe)	SLC16A10 (L270F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457408	NM_018593.5(SLC16A10):c.956A>G (p.Asn319Ser)	SLC16A10 (N319S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231249	NM_018593.5(SLC16A10):c.1043G>A (p.Arg348Gln)	SLC16A10 (R348Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318910	NM_018593.5(SLC16A10):c.1066G>A (p.Val356Met)	SLC16A10 (V356M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245644	NM_018593.5(SLC16A10):c.1102T>G (p.Phe368Val)	SLC16A10 (F368V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 761212	NM_018593.5(SLC16A10):c.1111C>T (p.Leu371=)	SLC16A10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2236837	NM_018593.5(SLC16A10):c.1114A>C (p.Met372Leu)	SLC16A10 (M372L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163051	NM_018593.5(SLC16A10):c.1157T>C (p.Ile386Thr)	SLC16A10 (I386T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163052	NM_018593.5(SLC16A10):c.1174A>C (p.Met392Leu)	SLC16A10 (M392L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326186	NM_018593.5(SLC16A10):c.1247T>A (p.Val416Asp)	SLC16A10 (V416D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163053	NM_018593.5(SLC16A10):c.1259T>C (p.Ile420Thr)	SLC16A10 (I420T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281470	NM_018593.5(SLC16A10):c.1409C>T (p.Pro470Leu)	SLC16A10 (P470L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615397	NM_018593.5(SLC16A10):c.1454G>C (p.Gly485Ala)	SLC16A10 (G485A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318907	NM_018593.5(SLC16A10):c.1475T>C (p.Met492Thr)	SLC16A10 (M492T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328973	NM_018593.5(SLC16A10):c.1491C>G (p.Asn497Lys)	SLC16A10 (N497K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3163054	NM_018593.5(SLC16A10):c.1495C>G (p.Leu499Val)	SLC16A10 (L499V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31