Related gene-specific medical variations for Gene (Select 55776) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3157977	NM_018322.3(SAYSD1):c.62C>T (p.Pro21Leu)	LOC129996373, SAYSD1 (P21L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3157974	NM_018322.3(SAYSD1):c.206A>T (p.Gln69Leu)	LOC129996373, SAYSD1 (Q69L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3157973	NM_018322.3(SAYSD1):c.193C>G (p.Pro65Ala)	LOC129996373, SAYSD1 (P65A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2548059	NM_018322.3(SAYSD1):c.149G>A (p.Arg50Gln)	LOC129996373, SAYSD1 (R50Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2391035	NM_018322.3(SAYSD1):c.44C>A (p.Ala15Glu)	LOC129996373, SAYSD1 (A15E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2355586	NM_018322.3(SAYSD1):c.125A>C (p.Lys42Thr)	LOC129996373, SAYSD1 (K42T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2343889	NM_018322.3(SAYSD1):c.61C>A (p.Pro21Thr)	LOC129996373, SAYSD1 (P21T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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