Related gene-specific medical variations for Gene (Select 10314) - ClinVar

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Links from Gene

Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290093	NM_006055.3(LANCL1):c.286C>G (p.Leu96Val)	LANCL1, LANCL1-AS1 (L96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290092	NM_006055.3(LANCL1):c.664G>A (p.Ala222Thr)	LANCL1, LANCL1-AS1 (A222T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290091	NM_006055.3(LANCL1):c.1007A>G (p.Tyr336Cys)	LANCL1, LANCL1-AS1 (Y336C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290090	NM_006055.3(LANCL1):c.970G>A (p.Gly324Ser)	LANCL1, LANCL1-AS1 (G324S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117775	NM_006055.3(LANCL1):c.835G>A (p.Ala279Thr)	LANCL1, LANCL1-AS1 (A279T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117771	NM_006055.3(LANCL1):c.464G>A (p.Arg155Gln)	LANCL1, LANCL1-AS1 (R155Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117769	NM_006055.3(LANCL1):c.236T>C (p.Phe79Ser)	LANCL1, LANCL1-AS1 (F79S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117768	NM_006055.3(LANCL1):c.205G>T (p.Ala69Ser)	LANCL1, LANCL1-AS1 (A69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622408	NM_006055.3(LANCL1):c.655C>T (p.His219Tyr)	LANCL1, LANCL1-AS1 (H219Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617907	NM_006055.3(LANCL1):c.992C>G (p.Ala331Gly)	LANCL1, LANCL1-AS1 (A331G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607539	NM_006055.3(LANCL1):c.871A>G (p.Lys291Glu)	LANCL1, LANCL1-AS1 (K291E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596629	NM_006055.3(LANCL1):c.452T>C (p.Met151Thr)	LANCL1, LANCL1-AS1 (M151T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550995	NM_006055.3(LANCL1):c.497A>G (p.Asn166Ser)	LANCL1, LANCL1-AS1 (N166S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524136	NM_006055.3(LANCL1):c.931C>A (p.Gln311Lys)	LANCL1, LANCL1-AS1 (Q311K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520846	NM_006055.3(LANCL1):c.853A>G (p.Met285Val)	LANCL1, LANCL1-AS1 (M285V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484657	NM_006055.3(LANCL1):c.265C>T (p.His89Tyr)	LANCL1, LANCL1-AS1 (H89Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463875	NM_006055.3(LANCL1):c.935A>G (p.Tyr312Cys)	LANCL1, LANCL1-AS1 (Y312C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456117	NM_006055.3(LANCL1):c.440C>A (p.Ala147Asp)	LANCL1, LANCL1-AS1 (A147D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383262	NM_006055.3(LANCL1):c.908A>G (p.Tyr303Cys)	LANCL1, LANCL1-AS1 (Y303C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363537	NM_006055.3(LANCL1):c.202A>T (p.Ile68Phe)	LANCL1, LANCL1-AS1 (I68F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313358	NM_006055.3(LANCL1):c.492T>G (p.Phe164Leu)	LANCL1, LANCL1-AS1 (F164L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304034	NM_006055.3(LANCL1):c.247G>A (p.Ala83Thr)	LANCL1, LANCL1-AS1 (A83T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294628	NM_006055.3(LANCL1):c.352G>A (p.Ala118Thr)	LANCL1, LANCL1-AS1 (A118T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289543	NM_006055.3(LANCL1):c.397T>C (p.Cys133Arg)	LANCL1, LANCL1-AS1 (C133R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262303	NM_006055.3(LANCL1):c.968A>C (p.His323Pro)	LANCL1, LANCL1-AS1 (H323P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250096	NM_006055.3(LANCL1):c.203T>C (p.Ile68Thr)	LANCL1, LANCL1-AS1 (I68T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244766	NM_006055.3(LANCL1):c.211C>T (p.Leu71Phe)	LANCL1, LANCL1-AS1 (L71F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243028	NM_006055.3(LANCL1):c.281A>G (p.Gln94Arg)	LANCL1, LANCL1-AS1 (Q94R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237817	NM_006055.3(LANCL1):c.1117T>C (p.Phe373Leu)	LANCL1, LANCL1-AS1 (F373L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781953	NM_006055.3(LANCL1):c.414T>G (p.Ile138Met)	LANCL1, LANCL1-AS1 (I138M)	Single nucleotide variant (missense variant)	not provided	GBenign

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Links from Gene

Items: 30