Related gene-specific medical variations for Gene (Select 83650) - ClinVar

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Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3164469	NM_054028.2(SLC35G5):c.81G>C (p.Trp27Cys)	MTMR9, SLC35G5 (W27C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164468	NM_054028.2(SLC35G5):c.745G>A (p.Asp249Asn)	MTMR9, SLC35G5 (D249N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164467	NM_054028.2(SLC35G5):c.673C>G (p.Leu225Val)	MTMR9, SLC35G5 (L225V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164466	NM_054028.2(SLC35G5):c.64C>G (p.Pro22Ala)	MTMR9, SLC35G5 (P22A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164465	NM_054028.2(SLC35G5):c.629A>T (p.Tyr210Phe)	MTMR9, SLC35G5 (Y210F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164464	NM_054028.2(SLC35G5):c.53C>T (p.Pro18Leu)	MTMR9, SLC35G5 (P18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164463	NM_054028.2(SLC35G5):c.388G>A (p.Ala130Thr)	MTMR9, SLC35G5 (A130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658402	NM_054028.2(SLC35G5):c.387C>T (p.Asn129=)	MTMR9, SLC35G5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2611245	NM_054028.2(SLC35G5):c.256C>G (p.Leu86Val)	MTMR9, SLC35G5 (L86V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566757	NM_054028.2(SLC35G5):c.400C>T (p.Arg134Cys)	MTMR9, SLC35G5 (R134C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552541	NM_054028.2(SLC35G5):c.455A>G (p.Gln152Arg)	MTMR9, SLC35G5 (Q152R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552017	NM_054028.2(SLC35G5):c.127G>T (p.Ala43Ser)	MTMR9, SLC35G5 (A43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543238	NM_054028.2(SLC35G5):c.245C>G (p.Pro82Arg)	MTMR9, SLC35G5 (P82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516273	NM_054028.2(SLC35G5):c.884T>C (p.Ile295Thr)	MTMR9, SLC35G5 (I295T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509077	NM_054028.2(SLC35G5):c.389C>A (p.Ala130Asp)	MTMR9, SLC35G5 (A130D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465121	NM_054028.2(SLC35G5):c.280C>G (p.Leu94Val)	MTMR9, SLC35G5 (L94V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456963	NM_054028.2(SLC35G5):c.97C>G (p.Pro33Ala)	MTMR9, SLC35G5 (P33A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410102	NM_054028.2(SLC35G5):c.113A>G (p.Asn38Ser)	MTMR9, SLC35G5 (N38S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349543	NM_054028.2(SLC35G5):c.787G>A (p.Ala263Thr)	MTMR9, SLC35G5 (A263T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346019	NM_054028.2(SLC35G5):c.337C>T (p.Leu113Phe)	MTMR9, SLC35G5 (L113F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323112	NM_054028.2(SLC35G5):c.188A>G (p.Gln63Arg)	MTMR9, SLC35G5 (Q63R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300675	NM_054028.2(SLC35G5):c.900G>C (p.Met300Ile)	MTMR9, SLC35G5 (M300I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280887	NM_054028.2(SLC35G5):c.55C>A (p.Pro19Thr)	MTMR9, SLC35G5 (P19T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255046	NM_054028.2(SLC35G5):c.529C>G (p.Leu177Val)	MTMR9, SLC35G5 (L177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212595	NM_054028.2(SLC35G5):c.406G>T (p.Gly136Cys)	MTMR9, SLC35G5 (G136C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 25