Related gene-specific medical variations for Gene (Select 3182) - ClinVar

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Links from Gene

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284551	NM_031266.3(HNRNPAB):c.734G>A (p.Arg245His)	HNRNPAB, PHYKPL (R245H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284550	NM_031266.3(HNRNPAB):c.901T>C (p.Tyr301His)	HNRNPAB, PHYKPL (Y301H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284549	NM_031266.3(HNRNPAB):c.67G>A (p.Val23Ile)	HNRNPAB, LOC129995413 (V23I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284548	NM_031266.3(HNRNPAB):c.733C>T (p.Arg245Cys)	HNRNPAB, PHYKPL (R245C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284547	NM_031266.3(HNRNPAB):c.904G>A (p.Gly302Ser)	HNRNPAB, PHYKPL (G302S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284546	NM_031266.3(HNRNPAB):c.35C>T (p.Thr12Met)	HNRNPAB, LOC129995413 (T12M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106388	NM_031266.3(HNRNPAB):c.743G>A (p.Arg248His)	HNRNPAB, PHYKPL (R248H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106382	NM_031266.3(HNRNPAB):c.127G>A (p.Ala43Thr)	HNRNPAB, LOC129995414 (A43T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615995	NM_031266.3(HNRNPAB):c.818G>A (p.Gly273Asp)	HNRNPAB, PHYKPL (G273D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602147	NM_031266.3(HNRNPAB):c.916G>A (p.Gly306Ser)	HNRNPAB, PHYKPL (G306S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570303	NM_031266.3(HNRNPAB):c.899A>G (p.Tyr300Cys)	HNRNPAB, PHYKPL (Y300C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2562086	NM_031266.3(HNRNPAB):c.134C>T (p.Ala45Val)	HNRNPAB, LOC129995414 (A45V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348630	NM_031266.3(HNRNPAB):c.19G>A (p.Glu7Lys)	HNRNPAB, LOC129995413 (E7K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332251	NM_031266.3(HNRNPAB):c.201G>C (p.Glu67Asp)	HNRNPAB, LOC129995414 (E67D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309401	NM_031266.3(HNRNPAB):c.55G>C (p.Gly19Arg)	HNRNPAB, LOC129995413 (G19R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270523	NM_031266.3(HNRNPAB):c.617A>C (p.Glu206Ala)	HNRNPAB, PHYKPL (E206A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270522	NM_031266.3(HNRNPAB):c.616G>C (p.Glu206Gln)	HNRNPAB, PHYKPL (E206Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249174	NM_031266.3(HNRNPAB):c.88G>C (p.Ala30Pro)	HNRNPAB, LOC129995413 (A30P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243452	NM_031266.3(HNRNPAB):c.30G>A (p.Met10Ile)	HNRNPAB, LOC129995413 (M10I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214165	NM_031266.3(HNRNPAB):c.880G>A (p.Asp294Asn)	HNRNPAB, PHYKPL (D294N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 20