ACSM3[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140492	NM_005622.4(ACSM3):c.11G>T (p.Arg4Leu)	ACSM3 (R4L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140538	NM_005622.4(ACSM3):c.32G>A (p.Arg11His)	ACSM3 (R11H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2646285	NM_005622.4(ACSM3):c.75G>A (p.Val25=)	ACSM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2646286	NM_005622.4(ACSM3):c.93T>C (p.Asp31=)	ACSM3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3140502	NM_005622.4(ACSM3):c.130G>C (p.Glu44Gln)	ACSM3 (E44Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516104	NM_005622.4(ACSM3):c.202T>G (p.Trp68Gly)	ACSM3 (W68G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375733	NM_005622.4(ACSM3):c.364C>T (p.Arg122Trp)	ACSM3 (R122W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263157	NM_005622.4(ACSM3):c.370A>T (p.Ile124Phe)	ACSM3 (I124F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263206	NM_005622.4(ACSM3):c.415G>A (p.Ala139Thr)	ACSM3 (A139T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263165	NM_005622.4(ACSM3):c.547G>A (p.Ala183Thr)	ACSM3 (A183T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348981	NM_005622.4(ACSM3):c.563G>C (p.Cys188Ser)	ACSM3 (C188S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321053	NM_005622.4(ACSM3):c.627G>C (p.Lys209Asn)	ACSM3 (K209N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance