6058[HGNC] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1239350	NM_001040694.2(INCENP):c.-11-179del	INCENP	Deletion (intron variant)	not provided	GBenign
Select item 1272951	NM_001040694.2(INCENP):c.-11-175del	INCENP	Deletion (intron variant)	not provided	GBenign
Select item 1179975	NM_001040694.2(INCENP):c.-11-147G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221642	NM_001040694.2(INCENP):c.-11-82A>G	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3109612	NM_001040694.2(INCENP):c.11C>T (p.Thr4Met)	INCENP (T4M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109619	NM_001040694.2(INCENP):c.16C>T (p.Pro6Ser)	INCENP (P6S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477822	NM_001040694.2(INCENP):c.37G>A (p.Glu13Lys)	INCENP (E13K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283848	NM_001040694.2(INCENP):c.85A>G (p.Lys29Glu)	INCENP (K29E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1279221	NM_001040694.2(INCENP):c.108A>G (p.Glu36=)	INCENP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2589532	NM_001040694.2(INCENP):c.121G>T (p.Ala41Ser)	INCENP (A41S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397481	NM_001040694.2(INCENP):c.128G>A (p.Arg43His)	INCENP (R43H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1242936	NM_001040694.2(INCENP):c.141-27G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3109618	NM_001040694.2(INCENP):c.158C>T (p.Pro53Leu)	INCENP (P53L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340338	NM_001040694.2(INCENP):c.176C>T (p.Thr59Ile)	INCENP (T59I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510731	NM_001040694.2(INCENP):c.194G>A (p.Arg65Gln)	INCENP (R65Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1282557	NM_001040694.2(INCENP):c.254+234T>G	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256968	NM_001040694.2(INCENP):c.255-181C>T	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181058	NM_001040694.2(INCENP):c.255-57C>T	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2224861	NM_001040694.2(INCENP):c.255G>T (p.Arg85Ser)	INCENP (R85S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109632	NM_001040694.2(INCENP):c.274C>T (p.Arg92Trp)	INCENP (R92W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406174	NM_001040694.2(INCENP):c.275G>A (p.Arg92Gln)	INCENP (R92Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271692	NM_001040694.2(INCENP):c.287T>C (p.Leu96Pro)	INCENP (L96P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494663	NM_001040694.2(INCENP):c.293C>T (p.Ser98Phe)	INCENP (S98F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509565	NM_001040694.2(INCENP):c.296G>A (p.Arg99Gln)	INCENP (R99Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 779201	NM_001040694.2(INCENP):c.299G>A (p.Arg100His)	INCENP (R100H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2608739	NM_001040694.2(INCENP):c.327G>T (p.Lys109Asn)	INCENP (K109N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1243072	NM_001040694.2(INCENP):c.360C>T (p.Val120=)	INCENP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2254928	NM_001040694.2(INCENP):c.377G>A (p.Arg126His)	INCENP (R126H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109633	NM_001040694.2(INCENP):c.383C>T (p.Ala128Val)	INCENP (A128V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362993	NM_001040694.2(INCENP):c.397G>A (p.Ala133Thr)	INCENP (A133T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774693	NM_001040694.2(INCENP):c.405C>T (p.Thr135=)	INCENP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1287033	NM_001040694.2(INCENP):c.410C>T (p.Ala137Val)	INCENP (A137V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3109634	NM_001040694.2(INCENP):c.416C>T (p.Ala139Val)	INCENP (A139V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776619	NM_001040694.2(INCENP):c.469G>A (p.Glu157Lys)	INCENP (E157K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2481784	NM_001040694.2(INCENP):c.496G>T (p.Val166Leu)	INCENP (V166L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350955	NM_001040694.2(INCENP):c.527G>A (p.Arg176His)	INCENP (R176H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285993	NM_001040694.2(INCENP):c.560T>C (p.Met187Thr)	INCENP (M187T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508426	NM_001040694.2(INCENP):c.568G>A (p.Glu190Lys)	INCENP (E190K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243517	NM_001040694.2(INCENP):c.619A>G (p.Thr207Ala)	INCENP (T207A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109635	NM_001040694.2(INCENP):c.622T>C (p.Ser208Pro)	INCENP (S208P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408041	NM_001040694.2(INCENP):c.716C>T (p.Thr239Ile)	INCENP (T239I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395283	NM_001040694.2(INCENP):c.740G>T (p.Gly247Val)	INCENP (G247V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641840	NM_001040694.2(INCENP):c.754C>T (p.Arg252Trp)	INCENP (R252W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2338473	NM_001040694.2(INCENP):c.812C>G (p.Ala271Gly)	INCENP (A271G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2360578	NM_001040694.2(INCENP):c.839G>A (p.Arg280Gln)	INCENP (R280Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493364	NM_001040694.2(INCENP):c.841G>A (p.Val281Met)	INCENP (V281M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402968	NM_001040694.2(INCENP):c.841G>T (p.Val281Leu)	INCENP (V281L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540369	NM_001040694.2(INCENP):c.874A>G (p.Thr292Ala)	INCENP (T292A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641841	NM_001040694.2(INCENP):c.876G>A (p.Thr292=)	INCENP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3109636	NM_001040694.2(INCENP):c.908T>G (p.Val303Gly)	INCENP (V303G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229932	NM_001040694.2(INCENP):c.925G>A (p.Ala309Thr)	INCENP (A309T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109637	NM_001040694.2(INCENP):c.938C>T (p.Pro313Leu)	INCENP (P313L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109638	NM_001040694.2(INCENP):c.949G>A (p.Val317Ile)	INCENP (V317I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285991	NM_001040694.2(INCENP):c.998G>T (p.Arg333Leu)	INCENP (R333L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216613	NM_001040694.2(INCENP):c.1022A>G (p.Lys341Arg)	INCENP (K341R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602342	NM_001040694.2(INCENP):c.1045G>C (p.Ala349Pro)	INCENP (A349P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1224699	NM_001040694.2(INCENP):c.1063+112T>C	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280590	NM_001040694.2(INCENP):c.1063+130G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641842	NM_001040694.2(INCENP):c.1064-5C>G	INCENP	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2528388	NM_001040694.2(INCENP):c.1111G>T (p.Val371Phe)	INCENP (V371F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1253363	NM_001040694.2(INCENP):c.1116-200G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 780978	NM_001040694.2(INCENP):c.1147G>A (p.Glu383Lys)	INCENP (E383K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2532610	NM_001040694.2(INCENP):c.1154T>G (p.Val385Gly)	INCENP (V385G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1274767	NM_001040694.2(INCENP):c.1173+57A>G	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261519	NM_001040694.2(INCENP):c.1188T>C (p.Asn396=)	INCENP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2341950	NM_001040694.2(INCENP):c.1217C>T (p.Thr406Met)	INCENP (T406M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289981	NM_001040694.2(INCENP):c.1225G>A (p.Ala409Thr)	INCENP (A409T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1271598	NM_001040694.2(INCENP):c.1291+61G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252602	NM_001040694.2(INCENP):c.1292-75T>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3285990	NM_001040694.2(INCENP):c.1301C>T (p.Thr434Met)	INCENP (T434M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1235427	NM_001040694.2(INCENP):c.1302G>A (p.Thr434=)	INCENP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1294773	NM_001040694.2(INCENP):c.1343+64C>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236798	NM_001040694.2(INCENP):c.1343+152A>G	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245161	NM_001040694.2(INCENP):c.1344-207C>T	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294774	NM_001040694.2(INCENP):c.1344-154G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3109613	NM_001040694.2(INCENP):c.1345A>G (p.Arg449Gly)	INCENP (R449G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340941	NM_001040694.2(INCENP):c.1352G>A (p.Arg451His)	INCENP (R451H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407759	NM_001040694.2(INCENP):c.1387G>C (p.Glu463Gln)	INCENP (E463Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376106	NM_001040694.2(INCENP):c.1435C>G (p.Pro479Ala)	INCENP (P479A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390611	NM_001040694.2(INCENP):c.1448G>T (p.Cys483Phe)	INCENP (C483F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109616	NM_001040694.2(INCENP):c.1477C>T (p.Arg493Trp)	INCENP (R493W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109617	NM_001040694.2(INCENP):c.1486C>G (p.Leu496Val)	INCENP (L496V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1289748	NM_001040694.2(INCENP):c.1517T>C (p.Met506Thr)	INCENP (M506T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2340798	NM_001040694.2(INCENP):c.1518G>A (p.Met506Ile)	INCENP (M506I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217416	NM_001040694.2(INCENP):c.1543G>A (p.Val515Ile)	INCENP (V515I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1263734	NM_001040694.2(INCENP):c.1593+8G>T	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289667	NM_001040694.2(INCENP):c.1593+156G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263163	NM_001040694.2(INCENP):c.1606-244C>T	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244838	NM_001040694.2(INCENP):c.1606-54G>A	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2384569	NM_001040694.2(INCENP):c.1615C>T (p.Arg539Trp)	INCENP (R535W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357148	NM_001040694.2(INCENP):c.1616G>A (p.Arg539Gln)	INCENP (R539Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299867	NM_001040694.2(INCENP):c.1670A>T (p.Gln557Leu)	INCENP (Q557L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399742	NM_001040694.2(INCENP):c.1690C>T (p.Arg564Trp)	INCENP (R560W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283432	NM_001040694.2(INCENP):c.1732C>G (p.Leu578Val)	INCENP (L574V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285992	NM_001040694.2(INCENP):c.1735C>T (p.Arg579Cys)	INCENP (R579C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528478	NM_001040694.2(INCENP):c.1748A>G (p.Gln583Arg)	INCENP (Q583R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255896	NM_001040694.2(INCENP):c.1783A>C (p.Lys595Gln)	INCENP (K591Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408824	NM_001040694.2(INCENP):c.1828A>G (p.Thr610Ala)	INCENP (T606A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1288289	NM_001040694.2(INCENP):c.1837-22C>T	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262058	NM_001040694.2(INCENP):c.1837-10G>C	INCENP	Single nucleotide variant (intron variant)	not provided	GBenign

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