Related gene-specific medical variations for Gene (Select 11100) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284589	NM_007040.6(HNRNPUL1):c.50G>C (p.Arg17Pro)	HNRNPUL1, LOC130064499 (R17P)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3106447	NM_007040.6(HNRNPUL1):c.1776G>T (p.Arg592Ser)	HNRNPUL1, LOC130064502 (R592S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622333	NM_007040.6(HNRNPUL1):c.1916G>A (p.Arg639His)	HNRNPUL1, LOC130064502 (R550H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559085	NM_007040.6(HNRNPUL1):c.129C>G (p.Asp43Glu)	HNRNPUL1, LOC130064499 (D43E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2556829	NM_007040.6(HNRNPUL1):c.1921G>A (p.Gly641Ser)	HNRNPUL1, LOC130064502 (G541S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554873	NM_007040.6(HNRNPUL1):c.1751G>A (p.Arg584Gln)	HNRNPUL1, LOC130064502 (R484Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543840	NM_007040.6(HNRNPUL1):c.98T>C (p.Leu33Pro)	HNRNPUL1, LOC130064499 (L33P)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2528259	NM_007040.6(HNRNPUL1):c.1915C>T (p.Arg639Cys)	HNRNPUL1, LOC130064502 (R539C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526119	NM_007040.6(HNRNPUL1):c.64A>C (p.Thr22Pro)	HNRNPUL1, LOC130064499 (T22P)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2468922	NM_007040.6(HNRNPUL1):c.1934G>A (p.Arg645Gln)	HNRNPUL1, LOC130064502 (R545Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362035	NM_007040.6(HNRNPUL1):c.148G>A (p.Ala50Thr)	HNRNPUL1, LOC130064499 (A50T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2254074	NM_007040.6(HNRNPUL1):c.1739T>C (p.Ile580Thr)	HNRNPUL1, LOC130064502 (I491T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1701791	NM_007040.6(HNRNPUL1):c.1522A>G (p.Asn508Asp)	HNRNPUL1, LOC126862911 (N408D +2 more)	Single nucleotide variant (missense variant)	not provided	Gnot provided