"Ambry Genetics"[submitter] AND "LOC101928191"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2270115	NM_001040274.3(SYCP2L):c.1723C>A (p.Gln575Lys)	LOC101928191, SYCP2L (Q575K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367118	NM_001040274.3(SYCP2L):c.1724A>G (p.Gln575Arg)	LOC101928191, SYCP2L (Q575R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226790	NM_001040274.3(SYCP2L):c.1805A>G (p.Gln602Arg)	LOC101928191, SYCP2L (Q602R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172584	NM_001040274.3(SYCP2L):c.1838G>A (p.Ser613Asn)	LOC101928191, SYCP2L (S613N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260159	NM_001040274.3(SYCP2L):c.1850C>T (p.Ser617Phe)	LOC101928191, SYCP2L (S617F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172585	NM_001040274.3(SYCP2L):c.1880C>T (p.Pro627Leu)	LOC101928191, SYCP2L (P627L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172586	NM_001040274.3(SYCP2L):c.1886T>C (p.Ile629Thr)	LOC101928191, SYCP2L (I629T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2536190	NM_001040274.3(SYCP2L):c.1901C>T (p.Ser634Leu)	LOC101928191, SYCP2L (S634L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606198	NM_001040274.3(SYCP2L):c.1909G>C (p.Glu637Gln)	LOC101928191, SYCP2L (E637Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392141	NM_001040274.3(SYCP2L):c.1924A>G (p.Lys642Glu)	LOC101928191, SYCP2L (K642E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355966	NM_001040274.3(SYCP2L):c.1934T>G (p.Leu645Arg)	LOC101928191, SYCP2L (L645R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance