ClinVar for Gene (Select 7071) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3288803	NM_005655.4(KLF10):c.1423A>G (p.Thr475Ala)	KLF10 (T464A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3288802	NM_005655.4(KLF10):c.244C>G (p.Pro82Ala)	KLF10 (P71A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115262	NM_005655.4(KLF10):c.205T>C (p.Ser69Pro)	KLF10 (S58P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063013	GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	AARD, ABRA +665 more	Copy number gain	not specified	GPathogenic
Select item 3035444	NM_005655.4(KLF10):c.777A>C (p.Pro259=)	KLF10	Single nucleotide variant (synonymous variant)	KLF10-related disorder	GLikely benign
Select item 3019479	NM_005655.4(KLF10):c.847A>C (p.Asn283His)	KLF10 (N272H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3017755	NM_005655.4(KLF10):c.598A>G (p.Ile200Val)	KLF10 (I189V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3010995	NM_005655.4(KLF10):c.1184-16T>G	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2996848	NM_005655.4(KLF10):c.388A>G (p.Ile130Val)	KLF10 (I119V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2986829	NM_005655.4(KLF10):c.867C>T (p.Val289=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2983021	NM_005655.4(KLF10):c.1021C>G (p.Leu341Val)	KLF10 (L330V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975824	NM_005655.4(KLF10):c.1176G>A (p.Thr392=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2974764	NM_005655.4(KLF10):c.153T>C (p.Ser51=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2969365	NM_005655.4(KLF10):c.408G>C (p.Glu136Asp)	KLF10 (E125D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2961522	NM_005655.4(KLF10):c.1107C>T (p.His369=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2912634	NM_005655.4(KLF10):c.539A>G (p.Tyr180Cys)	KLF10 (Y180C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2906398	NM_005655.4(KLF10):c.812C>G (p.Pro271Arg)	KLF10 (P260R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2893479	NM_005655.4(KLF10):c.686A>T (p.Tyr229Phe)	KLF10 (Y218F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2891293	NM_005655.4(KLF10):c.1060G>A (p.Ala354Thr)	KLF10 (A343T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2881675	NM_005655.4(KLF10):c.1129G>A (p.Gly377Ser)	KLF10 (G366S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2880509	NM_005655.4(KLF10):c.315A>G (p.Gln105=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2880110	NM_005655.4(KLF10):c.239G>C (p.Gly80Ala)	KLF10 (G69A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2878744	NM_005655.4(KLF10):c.813G>A (p.Pro271=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872154	NM_005655.4(KLF10):c.437A>G (p.Lys146Arg)	KLF10 (K135R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2848250	NM_005655.4(KLF10):c.909C>T (p.Pro303=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2820110	NM_005655.4(KLF10):c.911C>G (p.Pro304Arg)	KLF10 (P293R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2765703	NM_005655.4(KLF10):c.873C>T (p.Pro291=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2764707	NM_005655.4(KLF10):c.1023C>G (p.Leu341=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2759409	NM_005655.4(KLF10):c.78T>A (p.Ser26Arg)	KLF10 (S26R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2756842	NM_005655.4(KLF10):c.1220A>G (p.Glu407Gly)	KLF10 (E396G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2741269	NM_005655.4(KLF10):c.868G>A (p.Val290Ile)	KLF10 (V290I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2740229	NM_005655.4(KLF10):c.36+2T>C	KLF10	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 2732311	NM_005655.4(KLF10):c.137T>C (p.Met46Thr)	KLF10 (M35T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2728026	NM_005655.4(KLF10):c.88T>C (p.Trp30Arg)	KLF10 (W30R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2726719	NM_005655.4(KLF10):c.159G>A (p.Lys53=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2725522	NM_005655.4(KLF10):c.1090T>A (p.Ser364Thr)	KLF10 (S353T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2721576	NM_005655.4(KLF10):c.1305C>T (p.Asp435=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2718915	NM_005655.4(KLF10):c.685T>G (p.Tyr229Asp)	KLF10 (Y218D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2716944	NM_005655.4(KLF10):c.620C>T (p.Pro207Leu)	KLF10 (P196L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689316	NM_005655.4(KLF10):c.1343C>G (p.Ala448Gly)	KLF10 (A437G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658734	NM_005655.4(KLF10):c.367_368del (p.Ser123fs)	KLF10 (S112fs +1 more)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 2628901	NM_005655.4(KLF10):c.1007C>T (p.Pro336Leu)	KLF10 (P325L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2553090	NM_005655.4(KLF10):c.722G>T (p.Cys241Phe)	KLF10 (C241F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2426944	NC_000008.10:g.(?_98358247)_(106815766_?)dup	ANKRD46, ATP6V1C1 +40 more	Duplication	not provided	GUncertain significance
Select item 2321613	NM_005655.4(KLF10):c.661G>T (p.Asp221Tyr)	KLF10 (D221Y +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2313595	NM_005655.4(KLF10):c.1421C>T (p.Pro474Leu)	KLF10 (P474L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297187	NM_005655.4(KLF10):c.346A>C (p.Thr116Pro)	KLF10 (T105P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266063	NM_005655.4(KLF10):c.1027C>A (p.Pro343Thr)	KLF10 (P332T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242260	NM_005655.4(KLF10):c.1175C>T (p.Thr392Met)	KLF10 (T381M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2202356	NM_005655.4(KLF10):c.596A>G (p.Asn199Ser)	KLF10 (N188S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2195630	NM_005655.4(KLF10):c.720C>T (p.Ile240=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2194518	NM_005655.4(KLF10):c.1169C>T (p.Thr390Met)	KLF10 (T390M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2189173	NM_005655.4(KLF10):c.423A>G (p.Pro141=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2184595	NM_005655.4(KLF10):c.1183+5C>G	KLF10	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2175672	NM_005655.4(KLF10):c.206C>G (p.Ser69Cys)	KLF10 (S58C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2174518	NM_005655.4(KLF10):c.960G>C (p.Val320=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2164875	NM_005655.4(KLF10):c.771C>G (p.Val257=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2163647	NM_005655.4(KLF10):c.259A>G (p.Ile87Val)	KLF10 (I87V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2156884	NM_005655.4(KLF10):c.54G>T (p.Met18Ile)	KLF10 (M18I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2148946	NM_005655.4(KLF10):c.390T>A (p.Ile130=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2146715	NM_005655.4(KLF10):c.696T>C (p.Ser232=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2143671	NM_005655.4(KLF10):c.69A>G (p.Pro23=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2132353	NM_005655.4(KLF10):c.132A>G (p.Ala44=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2126155	NM_005655.4(KLF10):c.793G>T (p.Gly265Trp)	KLF10 (G254W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2113675	NM_005655.4(KLF10):c.438del (p.Lys146fs)	KLF10 (K135fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2107616	NM_005655.4(KLF10):c.746_747delinsTG (p.Ser249Leu)	KLF10 (S249L +1 more)	Indel (missense variant)	not provided	GUncertain significance
Select item 2107500	NM_005655.4(KLF10):c.674G>A (p.Ser225Asn)	KLF10 (S225N +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2104057	NM_005655.4(KLF10):c.225G>C (p.Glu75Asp)	KLF10 (E75D +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2103133	NM_005655.4(KLF10):c.593A>G (p.Lys198Arg)	KLF10 (K187R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2092021	NM_005655.4(KLF10):c.554T>C (p.Phe185Ser)	KLF10 (F174S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2086489	NM_005655.4(KLF10):c.1288G>A (p.Ala430Thr)	KLF10 (A419T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2078756	NM_005655.4(KLF10):c.1290G>A (p.Ala430=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2073618	NM_005655.4(KLF10):c.996G>A (p.Pro332=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2070925	NM_005655.4(KLF10):c.685T>C (p.Tyr229His)	KLF10 (Y218H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2068861	NM_005655.4(KLF10):c.420C>T (p.Ser140=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2062798	NM_005655.4(KLF10):c.651G>A (p.Val217=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2061709	NM_005655.4(KLF10):c.1071C>G (p.Val357=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2060619	NM_005655.4(KLF10):c.68C>T (p.Pro23Leu)	KLF10 (P12L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2059652	NM_005655.4(KLF10):c.1184-8del	KLF10	Deletion (intron variant)	not provided	GLikely benign
Select item 2057060	NM_005655.4(KLF10):c.383C>T (p.Pro128Leu)	KLF10 (P128L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2054707	NM_005655.4(KLF10):c.377C>G (p.Ala126Gly)	KLF10 (A115G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2050032	NM_005655.4(KLF10):c.237G>A (p.Pro79=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2046021	NM_005655.4(KLF10):c.577G>A (p.Val193Ile)	KLF10 (V182I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2043277	NM_005655.4(KLF10):c.656A>T (p.Asp219Val)	KLF10 (D219V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2041700	NM_005655.4(KLF10):c.177C>T (p.Tyr59=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2039834	NM_005655.4(KLF10):c.557G>A (p.Arg186Lys)	KLF10 (R175K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2036298	NM_005655.4(KLF10):c.499C>T (p.His167Tyr)	KLF10 (H156Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2035750	NM_005655.4(KLF10):c.119A>G (p.Glu40Gly)	KLF10 (E29G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2026763	NM_005655.4(KLF10):c.1349G>A (p.Arg450His)	KLF10 (R439H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2021754	NM_005655.4(KLF10):c.552T>G (p.Ser184=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2019581	NM_005655.4(KLF10):c.576T>C (p.Asn192=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2017487	NM_005655.4(KLF10):c.739C>A (p.Pro247Thr)	KLF10 (P247T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1997616	NM_005655.4(KLF10):c.875G>A (p.Ser292Asn)	KLF10 (S281N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1996233	NM_005655.4(KLF10):c.288C>T (p.Tyr96=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1992075	NM_005655.4(KLF10):c.887G>T (p.Ser296Ile)	KLF10 (S296I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1988347	NM_005655.4(KLF10):c.271-20T>C	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1987937	NM_005655.4(KLF10):c.864A>T (p.Thr288=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1985560	NM_005655.4(KLF10):c.394G>A (p.Ala132Thr)	KLF10 (A132T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1959950	NM_005655.4(KLF10):c.1076C>A (p.Pro359His)	KLF10 (P359H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1954128	NM_005655.4(KLF10):c.1184-11C>T	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign

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