SLC38A11[gene] and "single gene"[properties] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2327388	NM_001351537.2(SLC38A11):c.1363A>C (p.Thr455Pro)	SLC38A11 (T399P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456128	NM_001351537.2(SLC38A11):c.1360T>C (p.Ser454Pro)	SLC38A11 (S332P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601084	NM_001351537.2(SLC38A11):c.1355A>C (p.Gln452Pro)	SLC38A11 (Q452P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164555	NM_001351537.2(SLC38A11):c.1216G>T (p.Ala406Ser)	SLC38A11 (A284S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319701	NM_001351537.2(SLC38A11):c.1178C>T (p.Ser393Phe)	SLC38A11 (S315F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164563	NM_001351537.2(SLC38A11):c.1127T>C (p.Ile376Thr)	SLC38A11 (I181T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164561	NM_001351537.2(SLC38A11):c.1076G>A (p.Gly359Glu)	SLC38A11 (G359E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484440	NM_001351537.2(SLC38A11):c.1075G>A (p.Gly359Arg)	SLC38A11 (G303R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164560	NM_001351537.2(SLC38A11):c.961G>C (p.Glu321Gln)	SLC38A11 (E126Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390237	NM_001351537.2(SLC38A11):c.937C>T (p.Pro313Ser)	SLC38A11 (P235S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384729	NM_001351537.2(SLC38A11):c.929T>G (p.Leu310Trp)	SLC38A11 (L115W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515703	NM_001351537.2(SLC38A11):c.884A>T (p.Asp295Val)	SLC38A11 (D100V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319702	NM_001351537.2(SLC38A11):c.860T>C (p.Phe287Ser)	SLC38A11 (F209S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236389	NM_001351537.2(SLC38A11):c.814A>G (p.Thr272Ala)	SLC38A11 (T194A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396481	NM_001351537.2(SLC38A11):c.807C>G (p.Phe269Leu)	SLC38A11 (F269L +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3164559	NM_001351537.2(SLC38A11):c.803T>C (p.Ile268Thr)	SLC38A11 (I268T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615398	NM_001351537.2(SLC38A11):c.781G>A (p.Val261Met)	SLC38A11 (V261M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270233	NM_001351537.2(SLC38A11):c.721T>G (p.Tyr241Asp)	SLC38A11 (Y46D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249209	NM_001351537.2(SLC38A11):c.709T>G (p.Ser237Ala)	SLC38A11 (S115A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786867	NM_001351537.2(SLC38A11):c.689-10dup	SLC38A11	Duplication (intron variant)	not provided	GBenign
Select item 2530699	NM_001351537.2(SLC38A11):c.673G>A (p.Gly225Arg)	SLC38A11 (G30R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351126	NM_001351537.2(SLC38A11):c.553A>G (p.Thr185Ala)	SLC38A11 (T185A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348152	NM_001351537.2(SLC38A11):c.515G>A (p.Arg172Gln)	SLC38A11 (R116Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164558	NM_001351537.2(SLC38A11):c.479C>A (p.Ser160Tyr)	SLC38A11 (S38Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456312	NM_001351537.2(SLC38A11):c.478T>C (p.Ser160Pro)	SLC38A11 (S82P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164557	NM_001351537.2(SLC38A11):c.461A>G (p.His154Arg)	SLC38A11 (H154R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164556	NM_001351537.2(SLC38A11):c.448T>A (p.Phe150Ile)	SLC38A11 (F150I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294642	NM_001351537.2(SLC38A11):c.302A>G (p.Lys101Arg)	SLC38A11 (K101R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364924	NM_001351537.2(SLC38A11):c.262G>T (p.Ala88Ser)	SLC38A11 (A32S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164562	NM_001351537.2(SLC38A11):c.259G>A (p.Gly87Arg)	SLC38A11 (G31R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 30