NFRKB[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 75

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198389	NM_001143835.2(NFRKB):c.3824C>G (p.Ser1275Cys)	NFRKB (S1300C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198384	NM_001143835.2(NFRKB):c.3779G>A (p.Arg1260His)	NFRKB (R1285H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330736	NM_001143835.2(NFRKB):c.3661A>G (p.Ile1221Val)	NFRKB (I1246V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295858	NM_001143835.2(NFRKB):c.3628C>T (p.Leu1210Phe)	NFRKB (L1235F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494772	NM_001143835.2(NFRKB):c.3626A>G (p.Asn1209Ser)	NFRKB (N1234S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209022	NM_001143835.2(NFRKB):c.3583A>T (p.Met1195Leu)	NFRKB (M1220L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406496	NM_001143835.2(NFRKB):c.3484G>A (p.Val1162Met)	NFRKB (V1162M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299558	NM_001143835.2(NFRKB):c.3479C>G (p.Pro1160Arg)	NFRKB (P1160R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198368	NM_001143835.2(NFRKB):c.3475G>T (p.Ala1159Ser)	NFRKB (A1159S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307678	NM_001143835.2(NFRKB):c.3368C>A (p.Thr1123Asn)	NFRKB (T1148N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524943	NM_001143835.2(NFRKB):c.3348G>A (p.Ser1116=)	NFRKB	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2378138	NM_001143835.2(NFRKB):c.3310A>G (p.Thr1104Ala)	NFRKB (T1104A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491336	NM_001143835.2(NFRKB):c.3217G>A (p.Gly1073Arg)	NFRKB (G1073R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347589	NM_001143835.2(NFRKB):c.3169G>A (p.Ala1057Thr)	NFRKB (A1082T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198348	NM_001143835.2(NFRKB):c.3095C>T (p.Pro1032Leu)	NFRKB (P1032L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198347	NM_001143835.2(NFRKB):c.3033C>G (p.His1011Gln)	NFRKB (H1036Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198342	NM_001143835.2(NFRKB):c.2926A>G (p.Met976Val)	NFRKB (M1001V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299559	NM_001143835.2(NFRKB):c.2921C>T (p.Pro974Leu)	NFRKB (P999L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299553	NM_001143835.2(NFRKB):c.2869C>T (p.Pro957Ser)	NFRKB (P957S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198338	NM_001143835.2(NFRKB):c.2837G>A (p.Arg946His)	NFRKB (R971H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261449	NM_001143835.2(NFRKB):c.2663C>T (p.Pro888Leu)	NFRKB (P888L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299554	NM_001143835.2(NFRKB):c.2618G>A (p.Gly873Glu)	NFRKB (G873E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319499	NM_001143835.2(NFRKB):c.2588C>T (p.Thr863Met)	NFRKB (T888M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2642543	NM_001143835.2(NFRKB):c.2580G>T (p.Ala860=)	NFRKB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3198327	NM_001143835.2(NFRKB):c.2572G>A (p.Val858Ile)	NFRKB (V858I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384327	NM_001143835.2(NFRKB):c.2459C>T (p.Ser820Leu)	NFRKB (S820L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278065	NM_001143835.2(NFRKB):c.2449C>A (p.Pro817Thr)	NFRKB (P817T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2206543	NM_001143835.2(NFRKB):c.2443G>C (p.Ala815Pro)	NFRKB (A840P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475200	NM_001143835.2(NFRKB):c.2417G>A (p.Arg806Gln)	NFRKB (R806Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204847	NM_001143835.2(NFRKB):c.2405T>C (p.Leu802Pro)	NFRKB (L802P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365027	NM_001143835.2(NFRKB):c.2380G>A (p.Val794Met)	NFRKB (V794M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398661	NM_001143835.2(NFRKB):c.2375G>A (p.Arg792Gln)	NFRKB (R817Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3299556	NM_001143835.2(NFRKB):c.2371G>T (p.Ala791Ser)	NFRKB (A791S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405047	NM_001143835.2(NFRKB):c.2360C>A (p.Ser787Tyr)	NFRKB (S787Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198293	NM_001143835.2(NFRKB):c.2323A>G (p.Met775Val)	NFRKB (M800V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603670	NM_001143835.2(NFRKB):c.2276C>T (p.Ser759Leu)	NFRKB (S784L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198288	NM_001143835.2(NFRKB):c.2216C>T (p.Pro739Leu)	NFRKB (P764L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601123	NM_001143835.2(NFRKB):c.2207C>T (p.Ser736Phe)	NFRKB (S736F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291188	NM_001143835.2(NFRKB):c.2115G>C (p.Gln705His)	NFRKB (Q705H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238373	NM_001143835.2(NFRKB):c.2008G>A (p.Ala670Thr)	NFRKB (A670T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279212	NM_001143835.2(NFRKB):c.1714G>A (p.Asp572Asn)	NFRKB (D597N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198276	NM_001143835.2(NFRKB):c.1708C>T (p.Arg570Cys)	NFRKB (R570C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365012	NM_001143835.2(NFRKB):c.1616G>A (p.Arg539His)	NFRKB (R539H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528584	NM_001143835.2(NFRKB):c.1576C>T (p.Arg526Cys)	NFRKB (R551C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457146	NM_001143835.2(NFRKB):c.1541C>T (p.Thr514Met)	NFRKB (T514M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198265	NM_001143835.2(NFRKB):c.1512A>G (p.Val504=)	NFRKB	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3299555	NM_001143835.2(NFRKB):c.1375A>G (p.Lys459Glu)	NFRKB (K459E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299560	NM_001143835.2(NFRKB):c.1364C>T (p.Thr455Ile)	NFRKB (T455I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394193	NM_001143835.2(NFRKB):c.1344T>G (p.Phe448Leu)	NFRKB (F448L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541894	NM_001143835.2(NFRKB):c.1158C>G (p.Ile386Met)	NFRKB (I411M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615804	NM_001143835.2(NFRKB):c.1117A>G (p.Asn373Asp)	NFRKB (N398D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198242	NM_001143835.2(NFRKB):c.1108C>A (p.Leu370Ile)	NFRKB (L370I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299557	NM_001143835.2(NFRKB):c.1069G>A (p.Ala357Thr)	NFRKB (A357T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248764	NM_001143835.2(NFRKB):c.1027G>A (p.Val343Ile)	NFRKB (V343I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2331829	NM_001143835.2(NFRKB):c.1007C>T (p.Pro336Leu)	NFRKB (P336L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262107	NM_001143835.2(NFRKB):c.1001C>A (p.Ala334Asp)	NFRKB (A359D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211864	NM_001143835.2(NFRKB):c.929A>T (p.Lys310Ile)	NFRKB (K335I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335560	NM_001143835.2(NFRKB):c.874A>G (p.Asn292Asp)	NFRKB (N317D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198417	NM_001143835.2(NFRKB):c.854A>G (p.Asn285Ser)	NFRKB (N285S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2237753	NM_001143835.2(NFRKB):c.824C>T (p.Pro275Leu)	NFRKB (P275L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198408	NM_001143835.2(NFRKB):c.793C>G (p.His265Asp)	NFRKB (H265D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387511	NM_001143835.2(NFRKB):c.783A>T (p.Leu261Phe)	NFRKB (L286F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198403	NM_001143835.2(NFRKB):c.772A>G (p.Lys258Glu)	NFRKB (K258E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244894	NM_001143835.2(NFRKB):c.706G>A (p.Val236Met)	NFRKB (V261M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299551	NM_001143835.2(NFRKB):c.700C>T (p.Arg234Trp)	NFRKB (R234W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240326	NM_001143835.2(NFRKB):c.536G>A (p.Arg179His)	NFRKB (R192H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198399	NM_001143835.2(NFRKB):c.535C>T (p.Arg179Cys)	NFRKB (R179C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255034	NM_001143835.2(NFRKB):c.520C>T (p.Arg174Cys)	NFRKB (R174C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462357	NM_001143835.2(NFRKB):c.494G>T (p.Gly165Val)	NFRKB (G165V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378626	NM_001143835.2(NFRKB):c.492T>G (p.Ser164Arg)	NFRKB (S177R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588684	NM_001143835.2(NFRKB):c.290A>G (p.Asn97Ser)	NFRKB (N97S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507617	NM_001143835.2(NFRKB):c.200G>A (p.Arg67His)	NFRKB (R67H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254520	NM_001143835.2(NFRKB):c.68C>T (p.Thr23Met)	NFRKB (T23M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569191	NM_001143835.2(NFRKB):c.47C>T (p.Pro16Leu)	NFRKB (P29L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299550	NM_001143835.2(NFRKB):c.40C>T (p.Leu14Phe)	NFRKB (L27F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 75