Related gene-specific medical variations for Gene (Select 55290) - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3135041	NM_018310.4(BRF2):c.992A>T (p.Gln331Leu)	ADGRA2, BRF2 (Q331L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3135038	NM_018310.4(BRF2):c.1210A>G (p.Arg404Gly)	ADGRA2, BRF2 (R404G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3135037	NM_018310.4(BRF2):c.1186C>T (p.Pro396Ser)	ADGRA2, BRF2 (P396S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3135035	NM_018310.4(BRF2):c.1001G>A (p.Gly334Glu)	ADGRA2, BRF2 (G334E)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2594714	NM_018310.4(BRF2):c.1181G>A (p.Arg394His)	ADGRA2, BRF2 (R394H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2545195	NM_018310.4(BRF2):c.919C>G (p.Leu307Val)	ADGRA2, BRF2 (L307V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2522617	NM_018310.4(BRF2):c.138C>A (p.Asp46Glu)	BRF2, LOC130000208 (D46E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460904	NM_018310.4(BRF2):c.937C>T (p.Arg313Trp)	ADGRA2, BRF2 (R313W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2410376	NM_018310.4(BRF2):c.1103G>A (p.Arg368Gln)	ADGRA2, BRF2 (R368Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2409833	NM_018310.4(BRF2):c.1229A>G (p.Gln410Arg)	ADGRA2, BRF2 (Q410R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2404083	NM_018310.4(BRF2):c.1136C>T (p.Thr379Ile)	ADGRA2, BRF2 (T379I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2402740	NM_018310.4(BRF2):c.980C>T (p.Pro327Leu)	ADGRA2, BRF2 (P327L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2398304	NM_018310.4(BRF2):c.1102C>T (p.Arg368Trp)	ADGRA2, BRF2 (R368W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2374971	NM_018310.4(BRF2):c.1013T>G (p.Val338Gly)	ADGRA2, BRF2 (V338G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2368602	NM_018310.4(BRF2):c.1238C>T (p.Thr413Met)	ADGRA2, BRF2 (T413M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2363266	NM_018310.4(BRF2):c.1130C>T (p.Thr377Ile)	ADGRA2, BRF2 (T377I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2334704	NM_018310.4(BRF2):c.1112C>G (p.Pro371Arg)	ADGRA2, BRF2 (P371R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2252074	NM_018310.4(BRF2):c.1054G>T (p.Ala352Ser)	ADGRA2, BRF2 (A352S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2249327	NM_018310.4(BRF2):c.910C>G (p.Arg304Gly)	ADGRA2, BRF2 (R304G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2220201	NM_018310.4(BRF2):c.1213G>T (p.Ala405Ser)	ADGRA2, BRF2 (A405S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2216377	NM_018310.4(BRF2):c.1048C>T (p.Arg350Trp)	ADGRA2, BRF2 (R350W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 161715	NM_018310.4(BRF2):c.277G>A (p.Ala93Thr)	BRF2 (A93T)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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Links from Gene

Items: 22