"MFHAS1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056038	NM_004225.3(MFHAS1):c.3102G>A (p.Pro1034=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GBenign
Select item 3045962	NM_004225.3(MFHAS1):c.2772T>C (p.Pro924=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GLikely benign
Select item 3060793	NM_004225.3(MFHAS1):c.2537C>G (p.Ala846Gly)	MFHAS1 (A846G)	Single nucleotide variant (missense variant)	MFHAS1-related condition	GLikely benign
Select item 2658376	NM_004225.3(MFHAS1):c.2511G>A (p.Lys837=)	MFHAS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3034028	NM_004225.3(MFHAS1):c.2166C>T (p.Leu722=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GBenign
Select item 3050597	NM_004225.3(MFHAS1):c.1869C>G (p.Pro623=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GLikely benign
Select item 3043357	NM_004225.3(MFHAS1):c.1581G>A (p.Val527=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GLikely benign
Select item 3034595	NM_004225.3(MFHAS1):c.1014C>T (p.Ile338=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GLikely benign
Select item 3059717	NM_004225.3(MFHAS1):c.840C>G (p.Leu280=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GBenign
Select item 3034166	NM_004225.3(MFHAS1):c.579C>T (p.Leu193=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GBenign
Select item 776284	NM_004225.3(MFHAS1):c.236C>G (p.Pro79Arg)	MFHAS1 (P79R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3041711	NM_004225.3(MFHAS1):c.135C>T (p.Ala45=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GLikely benign
Select item 3059488	NM_004225.3(MFHAS1):c.102T>C (p.Leu34=)	MFHAS1	Single nucleotide variant (synonymous variant)	MFHAS1-related condition	GBenign