GALNT10[gene] and "single gene"[properties] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280527	NM_198321.4(GALNT10):c.71A>G (p.Asn24Ser)	GALNT10 (N24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098045	NM_198321.4(GALNT10):c.163T>A (p.Ser55Thr)	GALNT10 (S55T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402751	NM_198321.4(GALNT10):c.256C>T (p.Arg86Cys)	GALNT10 (R86C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 982122	NM_198321.4(GALNT10):c.263-139G>C	GALNT10	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 982123	NM_198321.4(GALNT10):c.263-138A>T	GALNT10	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 2509618	NM_198321.4(GALNT10):c.415C>T (p.Arg139Cys)	GALNT10 (R139C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238488	NM_198321.4(GALNT10):c.488G>T (p.Arg163Leu)	GALNT10 (R163L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248457	NM_198321.4(GALNT10):c.493G>A (p.Val165Ile)	GALNT10 (V165I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341235	NM_198321.4(GALNT10):c.509A>G (p.Asn170Ser)	GALNT10 (N170S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292502	NM_198321.4(GALNT10):c.523G>C (p.Glu175Gln)	GALNT10 (E175Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301611	NM_198321.4(GALNT10):c.529G>C (p.Val177Leu)	GALNT10 (V177L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487731	NM_198321.4(GALNT10):c.551A>C (p.Asp184Ala)	GALNT10 (D184A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391686	NM_198321.4(GALNT10):c.598A>G (p.Met200Val)	GALNT10 (M200V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294568	NM_198321.4(GALNT10):c.604C>T (p.Leu202Phe)	GALNT10 (L202F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279870	NM_198321.4(GALNT10):c.640C>T (p.Arg214Trp)	GALNT10 (R214W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394680	NM_198321.4(GALNT10):c.682G>T (p.Ala228Ser)	GALNT10 (A228S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213051	NM_198321.4(GALNT10):c.806T>C (p.Ile269Thr)	GALNT10 (I269T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623232	NM_198321.4(GALNT10):c.823C>T (p.Arg275Trp)	GALNT10 (R275W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371125	NM_198321.4(GALNT10):c.854G>A (p.Arg285Gln)	GALNT10 (R285Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098047	NM_198321.4(GALNT10):c.886C>T (p.Arg296Trp)	GALNT10 (R296W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098048	NM_198321.4(GALNT10):c.899C>T (p.Pro300Leu)	GALNT10 (P300L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21