Related gene-specific medical variations for Gene (Select 9144) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3451974	NM_004710.7(SYNGR2):c.13G>C (p.Ala5Pro)	LOC130061806, SYNGR2 (A5P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3451973	NM_004710.7(SYNGR2):c.53G>T (p.Arg18Leu)	LOC130061806, SYNGR2 (R18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3451969	NM_004710.7(SYNGR2):c.641C>A (p.Thr214Asn)	LOC130061808, SYNGR2 (P244T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3451968	NM_004710.7(SYNGR2):c.659C>T (p.Pro220Leu)	LOC130061808, SYNGR2 (P220L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3323946	NM_004710.7(SYNGR2):c.25G>A (p.Ala9Thr)	LOC130061806, SYNGR2 (A9T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549336	NM_004710.7(SYNGR2):c.88G>A (p.Ala30Thr)	LOC130061806, SYNGR2 (A30T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514070	NM_004710.7(SYNGR2):c.26C>G (p.Ala9Gly)	LOC130061806, SYNGR2 (A9G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406304	NM_004710.7(SYNGR2):c.635C>T (p.Ala212Val)	LOC130061808, SYNGR2 (R242W +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2222532	NM_004710.7(SYNGR2):c.88G>T (p.Ala30Ser)	LOC130061806, SYNGR2 (A30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance