"Ambry Genetics"[submitter] AND "LOC130003994"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2320557	NM_173555.4(TYSND1):c.974C>T (p.Pro325Leu)	LOC130003994, TYSND1 (P325L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228427	NM_173555.4(TYSND1):c.958C>G (p.Leu320Val)	LOC130003994, TYSND1 (L320V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330438	NM_173555.4(TYSND1):c.947G>A (p.Ser316Asn)	LOC130003994, TYSND1 (S316N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330436	NM_173555.4(TYSND1):c.933C>A (p.His311Gln)	LOC130003994, TYSND1 (H311Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540217	NM_173555.4(TYSND1):c.924C>A (p.Asp308Glu)	LOC130003994, TYSND1 (D308E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185285	NM_173555.4(TYSND1):c.852T>G (p.Cys284Trp)	LOC130003994, TYSND1 (C284W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479506	NM_173555.4(TYSND1):c.803C>T (p.Thr268Ile)	LOC130003994, TYSND1 (T268I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403259	NM_173555.4(TYSND1):c.764C>T (p.Ala255Val)	LOC130003994, TYSND1 (A255V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar