"Ambry Genetics"[submitter] AND "LOC130003038"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2481009	NM_032928.4(TMEM141):c.4G>C (p.Val2Leu)	LOC130003038, TMEM141 (V2L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511389	NM_032928.4(TMEM141):c.20C>T (p.Ser7Phe)	LOC130003038, TMEM141 (S7F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3326796	NM_032928.4(TMEM141):c.34G>A (p.Ala12Thr)	LOC130003038, TMEM141 (A12T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3178811	NM_032928.4(TMEM141):c.48G>C (p.Lys16Asn)	LOC130003038, TMEM141 (K16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382703	NM_032928.4(TMEM141):c.52C>T (p.Pro18Ser)	LOC130003038, TMEM141 (P18S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292908	NM_032928.4(TMEM141):c.55G>C (p.Gly19Arg)	LOC130003038, TMEM141 (G19R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471694	NM_032928.4(TMEM141):c.81G>C (p.Gln27His)	LOC130003038, TMEM141 (Q27H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590451	NM_032928.4(TMEM141):c.88G>T (p.Ala30Ser)	LOC130003038, TMEM141 (A30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar