Related gene-specific medical variations for Gene (Select 100507588) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2297421	NM_001419781.1(TGFBR3L):c.352C>T (p.Pro118Ser)	LOC130063397, TGFBR3L (P142S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271993	NM_001419781.1(TGFBR3L):c.325G>C (p.Asp109His)	LOC130063397, TGFBR3L (D133H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance