"PreventionGenetics, part of Exact Sciences"[submitter] AND "CMSS1"[ge - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053255	NM_001387850.1(FILIP1L):c.3382-2628C>T	CMSS1, FILIP1L	Single nucleotide variant (3 prime UTR variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3057961	NM_001387850.1(FILIP1L):c.3283T>C (p.Leu1095=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3045603	NM_001387850.1(FILIP1L):c.3245G>A (p.Ser1082Asn)	CMSS1, FILIP1L (S1082N +2 more)	Single nucleotide variant (missense variant +1 more)	FILIP1L-related condition	GBenign
Select item 3050131	NM_001387850.1(FILIP1L):c.2811G>C (p.Pro937=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3053214	NM_001387850.1(FILIP1L):c.2796T>C (p.Ser932=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3052659	NM_001387850.1(FILIP1L):c.2511C>T (p.Asp837=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3045387	NM_001387850.1(FILIP1L):c.2373C>T (p.Ser791=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GBenign
Select item 3053506	NM_001387850.1(FILIP1L):c.2235C>T (p.Val745=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GBenign
Select item 3046263	NM_001387850.1(FILIP1L):c.2083A>G (p.Thr695Ala)	CMSS1, FILIP1L (T271A +2 more)	Single nucleotide variant (missense variant +1 more)	FILIP1L-related condition	GBenign
Select item 3033680	NM_001387850.1(FILIP1L):c.1783T>C (p.Leu595=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GBenign
Select item 3052459	NM_001387850.1(FILIP1L):c.1332G>A (p.Leu444=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GBenign
Select item 3045633	NM_001387850.1(FILIP1L):c.1221G>A (p.Thr407=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3039661	NM_001387850.1(FILIP1L):c.1047G>A (p.Glu349=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3038733	NM_001387850.1(FILIP1L):c.750G>A (p.Thr250=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3039184	NM_001387850.1(FILIP1L):c.640C>G (p.Gln214Glu)	CMSS1, FILIP1L (Q214E)	Single nucleotide variant (missense variant +2 more)	FILIP1L-related condition	GBenign
Select item 3050264	NM_001387850.1(FILIP1L):c.504T>C (p.Arg168=)	CMSS1, FILIP1L	Single nucleotide variant (synonymous variant +1 more)	FILIP1L-related condition	GLikely benign
Select item 3059252	NM_001387850.1(FILIP1L):c.503G>A (p.Arg168His)	CMSS1, FILIP1L (R168H)	Single nucleotide variant (missense variant +1 more)	FILIP1L-related condition	GBenign
Select item 3043148	NM_032359.4(CMSS1):c.64+106369C>T	CMSS1, FILIP1L	Single nucleotide variant (intron variant)	CMSS1-related condition	GBenign
Select item 3033890	NM_001387850.1(FILIP1L):c.427-5C>T	CMSS1, FILIP1L	Single nucleotide variant (intron variant)	FILIP1L-related condition	GLikely benign