KLF10[gene] and "single gene"[properties] - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 209

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1232719	NM_005655.4(KLF10):c.*167C>T	KLF10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1181757	NM_005655.4(KLF10):c.*141C>T	KLF10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1704092	NM_005655.4(KLF10):c.*7G>A	KLF10	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1630931	NM_005655.4(KLF10):c.1428T>C (p.Pro476=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1545442	NM_005655.4(KLF10):c.1425C>T (p.Thr475=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 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 1443617	NM_005655.4(KLF10):c.1412C>T (p.Ala471Val)	KLF10 (A460V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1477025	NM_005655.4(KLF10):c.1410T>G (p.Ile470Met)	KLF10 (I459M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1927694	NM_005655.4(KLF10):c.1399C>T (p.Leu467=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1398172	NM_005655.4(KLF10):c.1368G>C (p.Lys456Asn)	KLF10 (K445N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1644979	NM_005655.4(KLF10):c.1356A>G (p.Leu452=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 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 1365625	NM_005655.4(KLF10):c.1310G>A (p.Arg437Gln)	KLF10 (R426Q +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 1584489	NM_005655.4(KLF10):c.1296C>T (p.Pro432=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 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 1605155	NM_005655.4(KLF10):c.1272G>A (p.Thr424=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1593787	NM_005655.4(KLF10):c.1257C>T (p.His419=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1602777	NM_005655.4(KLF10):c.1221A>G (p.Glu407=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 1351994	NM_005655.4(KLF10):c.1199G>A (p.Ser400Asn)	KLF10 (S389N +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 1954128	NM_005655.4(KLF10):c.1184-11C>T	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1594788	NM_005655.4(KLF10):c.1184-15A>G	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3010995	NM_005655.4(KLF10):c.1184-16T>G	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1554729	NM_005655.4(KLF10):c.1184-17G>T	KLF10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233652	NM_005655.4(KLF10):c.1184-233A>G	KLF10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1610539	NM_005655.4(KLF10):c.1183+19A>C	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1639256	NM_005655.4(KLF10):c.1183+17A>T	KLF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1553300	NM_005655.4(KLF10):c.1183+14C>G	KLF10	Single nucleotide variant (intron 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 2975824	NM_005655.4(KLF10):c.1176G>A (p.Thr392=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1555194	NM_005655.4(KLF10):c.1176G>C (p.Thr392=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
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 1641527	NM_005655.4(KLF10):c.1170G>A (p.Thr390=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
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 1645234	NM_005655.4(KLF10):c.1164C>T (p.Ala388=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 2961522	NM_005655.4(KLF10):c.1107C>T (p.His369=)	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 1589760	NM_005655.4(KLF10):c.1087T>G (p.Ser363Ala)	KLF10 (S352A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1520989	NM_005655.4(KLF10):c.1079A>G (p.Gln360Arg)	KLF10 (Q360R +1 more)	Single nucleotide variant (missense variant +1 more)	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 2061709	NM_005655.4(KLF10):c.1071C>G (p.Val357=)	KLF10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1446673	NM_005655.4(KLF10):c.1063G>T (p.Ala355Ser)	KLF10 (A344S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1391477	NM_005655.4(KLF10):c.1061C>T (p.Ala354Val)	KLF10 (A343V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	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 1405476	NM_005655.4(KLF10):c.1043C>T (p.Pro348Leu)	KLF10 (P337L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1483554	NM_005655.4(KLF10):c.1042C>G (p.Pro348Ala)	KLF10 (P337A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1590321	NM_005655.4(KLF10):c.1035C>T (p.Ala345=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2764707	NM_005655.4(KLF10):c.1023C>G (p.Leu341=)	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 1626728	NM_005655.4(KLF10):c.1011T>C (p.Asn337=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1585601	NM_005655.4(KLF10):c.1008G>A (p.Pro336=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 1421890	NM_005655.4(KLF10):c.1001T>C (p.Val334Ala)	KLF10 (V323A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2073618	NM_005655.4(KLF10):c.996G>A (p.Pro332=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2174518	NM_005655.4(KLF10):c.960G>C (p.Val320=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1478613	NM_005655.4(KLF10):c.946G>A (p.Ala316Thr)	KLF10 (A316T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1491593	NM_005655.4(KLF10):c.945C>T (p.Gly315=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1521027	NM_005655.4(KLF10):c.941A>G (p.Lys314Arg)	KLF10 (K303R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1533729	NM_005655.4(KLF10):c.921C>T (p.Phe307=)	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 1502126	NM_005655.4(KLF10):c.911C>A (p.Pro304His)	KLF10 (P304H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 1898738	NM_005655.4(KLF10):c.906C>T (p.Cys302=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1481928	NM_005655.4(KLF10):c.901G>A (p.Val301Ile)	KLF10 (V301I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1573854	NM_005655.4(KLF10):c.900C>T (p.Ala300=)	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 1374619	NM_005655.4(KLF10):c.884C>A (p.Pro295His)	KLF10 (P295H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1404524	NM_005655.4(KLF10):c.880C>T (p.Pro294Ser)	KLF10 (P294S +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 2765703	NM_005655.4(KLF10):c.873C>T (p.Pro291=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2986829	NM_005655.4(KLF10):c.867C>T (p.Val289=)	KLF10	Single nucleotide variant (synonymous 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 1659875	NM_005655.4(KLF10):c.861A>G (p.Thr287=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1416675	NM_005655.4(KLF10):c.860C>G (p.Thr287Arg)	KLF10 (T276R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1432202	NM_005655.4(KLF10):c.853G>A (p.Val285Ile)	KLF10 (V285I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1914306	NM_005655.4(KLF10):c.852T>C (p.Pro284=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	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 1588577	NM_005655.4(KLF10):c.819C>T (p.Ile273=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2878744	NM_005655.4(KLF10):c.813G>A (p.Pro271=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 1508301	NM_005655.4(KLF10):c.805C>T (p.Pro269Ser)	KLF10 (P258S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 1540236	NM_005655.4(KLF10):c.786A>G (p.Val262=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1354378	NM_005655.4(KLF10):c.784G>C (p.Val262Leu)	KLF10 (V251L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 2164875	NM_005655.4(KLF10):c.771C>G (p.Val257=)	KLF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1477314	NM_005655.4(KLF10):c.769G>A (p.Val257Ile)	KLF10 (V246I +1 more)	Single nucleotide variant (missense 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 1226451	NM_005655.4(KLF10):c.746C>T (p.Ser249Phe)	KLF10 (S238F +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
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 1522860	NM_005655.4(KLF10):c.725G>T (p.Arg242Met)	KLF10 (R231M +1 more)	Single nucleotide variant (missense variant)	not provided	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

<< First< Prev

Page of 3