Related gene-specific medical variations for Gene (Select 64783) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3313198	NM_022768.5(RBM15):c.2225C>T (p.Pro742Leu)	LOC112577475, RBM15 (P742L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313195	NM_022768.5(RBM15):c.19G>A (p.Asp7Asn)	LOC129931144, RBM15 (D7N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313191	NM_022768.5(RBM15):c.1906A>G (p.Arg636Gly)	LOC112577475, RBM15 (R636G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152202	NM_022768.5(RBM15):c.73A>G (p.Thr25Ala)	LOC129931144, RBM15 (T25A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152200	NM_022768.5(RBM15):c.29C>T (p.Pro10Leu)	LOC129931144, RBM15 (P10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152198	NM_022768.5(RBM15):c.2135G>C (p.Ser712Thr)	LOC112577475, RBM15 (S712T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152197	NM_022768.5(RBM15):c.2083C>T (p.Leu695Phe)	LOC112577475, RBM15 (L695F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152196	NM_022768.5(RBM15):c.2072C>T (p.Ser691Phe)	LOC112577475, RBM15 (S691F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152193	NM_022768.5(RBM15):c.104G>A (p.Arg35His)	LOC129931144, RBM15 (R35H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597257	NM_022768.5(RBM15):c.157G>C (p.Val53Leu)	LOC129931144, RBM15 (V53L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548208	NM_022768.5(RBM15):c.2197A>G (p.Thr733Ala)	LOC112577475, RBM15 (T733A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512177	NM_022768.5(RBM15):c.2060A>G (p.Asp687Gly)	LOC112577475, RBM15 (D687G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395995	NM_022768.5(RBM15):c.1840C>G (p.Leu614Val)	LOC112577475, RBM15 (L614V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387833	NM_022768.5(RBM15):c.61C>T (p.Pro21Ser)	LOC129931144, RBM15 (P21S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316768	NM_022768.5(RBM15):c.89G>A (p.Arg30Gln)	LOC129931144, RBM15 (R30Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310791	NM_022768.5(RBM15):c.2135G>A (p.Ser712Asn)	LOC112577475, RBM15 (S712N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299639	NM_022768.5(RBM15):c.1817C>G (p.Pro606Arg)	LOC112577475, RBM15 (P606R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297745	NM_022768.5(RBM15):c.49C>T (p.Arg17Trp)	LOC129931144, RBM15 (R17W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233108	NM_022768.5(RBM15):c.65T>A (p.Leu22Gln)	LOC129931144, RBM15 (L22Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215873	NM_022768.5(RBM15):c.32G>A (p.Arg11Gln)	LOC129931144, RBM15 (R11Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206185	NM_022768.5(RBM15):c.74C>G (p.Thr25Arg)	LOC129931144, RBM15 (T25R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 438785	NM_022768.5(RBM15):c.1912C>A (p.Gln638Lys)	LOC112577475, RBM15 (Q638K)	Single nucleotide variant (missense variant)	Neuroblastoma	Gother

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Links from Gene

Items: 22