26350[HGNC] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57301	GRCh38/hg38 2q31.1-33.2(chr2:174898848-203941548)x1	LOC129935164, LOC129935165 +697 more	Copy number loss	See cases	GPathogenic
Select item 155417	GRCh38/hg38 2q31.1-32.3(chr2:176086763-193201970)x1	AGPS, ANKAR +377 more	Copy number loss	See cases	GPathogenic
Select item 58770	GRCh38/hg38 2q31.1-33.1(chr2:176304445-202039790)x1	LOC126806416, LOC126806417 +591 more	Copy number loss	See cases	GPathogenic
Select item 153288	GRCh38/hg38 2q31.2-32.3(chr2:177827730-195125329)x1	ANKAR, ASDURF +312 more	Copy number loss	See cases	GPathogenic
Select item 58771	GRCh38/hg38 2q31.2-33.1(chr2:177874070-198525492)x1	ANKAR, ANKRD44 +430 more	Copy number loss	See cases	GPathogenic
Select item 150620	GRCh38/hg38 2q31.3-36.2(chr2:180513793-224302848)x3	INPP1, ITGA4 +1097 more	Copy number gain	See cases	GPathogenic
Select item 149200	GRCh38/hg38 2q31.3-32.3(chr2:181758701-192015392)x1	ANKAR, ASDURF +191 more	Copy number loss	See cases	GPathogenic
Select item 146616	GRCh38/hg38 2q32.1-33.1(chr2:186027472-201059372)x1	ANKAR, ANKRD44 +329 more	Copy number loss	See cases	GPathogenic
Select item 59158	GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3	LOC129935343, LOC129935344 +1703 more	Copy number gain	See cases	GPathogenic
Select item 146486	GRCh38/hg38 2q32.2(chr2:188947503-189689613)x1	ANKAR, ASDURF +19 more	Copy number loss	See cases	GPathogenic
Select item 154206	GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3	AAMP, ABCA12 +1687 more	Copy number gain	See cases	GPathogenic
Select item 145813	GRCh38/hg38 2q32.2(chr2:189442378-189689554)x3	ANKAR, ASDURF +8 more	Copy number gain	See cases	GLikely benign
Select item 2548686	NM_001378068.1(ANKAR):c.29C>G (p.Pro10Arg)	ANKAR (P10R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555649	NM_001378068.1(ANKAR):c.41A>G (p.Gln14Arg)	ANKAR (Q14R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 740450	NM_001378068.1(ANKAR):c.105dup (p.Glu36Ter)	ANKAR (E36*)	Duplication (nonsense)	not provided	GLikely benign
Select item 2373056	NM_001378068.1(ANKAR):c.185G>A (p.Arg62His)	ANKAR (R62H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482818	NM_001378068.1(ANKAR):c.248C>T (p.Ala83Val)	ANKAR (A83V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238516	NM_001378068.1(ANKAR):c.265G>A (p.Val89Met)	ANKAR (V89M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775795	NM_001378068.1(ANKAR):c.276T>G (p.Thr92=)	ANKAR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2208628	NM_001378068.1(ANKAR):c.281T>C (p.Leu94Pro)	ANKAR (L94P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791881	NM_001378068.1(ANKAR):c.281T>G (p.Leu94Arg)	ANKAR (L94R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3295510	NM_001378068.1(ANKAR):c.302A>G (p.His101Arg)	ANKAR (H101R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350404	NM_001378068.1(ANKAR):c.430G>A (p.Gly144Arg)	ANKAR (G144R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295530	NM_001378068.1(ANKAR):c.476A>T (p.His159Leu)	ANKAR (H159L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216628	NM_001378068.1(ANKAR):c.560C>T (p.Pro187Leu)	ANKAR (P187L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295494	NM_001378068.1(ANKAR):c.576C>G (p.Asp192Glu)	ANKAR (D192E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 716762	NM_001378068.1(ANKAR):c.616A>G (p.Thr206Ala)	ANKAR (T206A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3295570	NM_001378068.1(ANKAR):c.662A>G (p.Glu221Gly)	ANKAR (E221G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295559	NM_001378068.1(ANKAR):c.726T>G (p.Asn242Lys)	ANKAR (N242K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226307	NM_001378068.1(ANKAR):c.747C>G (p.Phe249Leu)	ANKAR (F249L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301484	NM_001378068.1(ANKAR):c.832G>T (p.Asp278Tyr)	ANKAR (D278Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120302	NM_001378068.1(ANKAR):c.915G>T (p.Lys305Asn)	ANKAR (K305N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489310	NM_001378068.1(ANKAR):c.992A>G (p.Lys331Arg)	ANKAR (K331R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295633	NM_001378068.1(ANKAR):c.1099T>A (p.Cys367Ser)	ANKAR (C367S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295548	NM_001378068.1(ANKAR):c.1171C>T (p.Pro391Ser)	ANKAR (P391S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478763	NM_001378068.1(ANKAR):c.1180G>A (p.Glu394Lys)	ANKAR (E394K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295613	NM_001378068.1(ANKAR):c.1288A>T (p.Met430Leu)	ANKAR (M430L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120180	NM_001378068.1(ANKAR):c.1289T>C (p.Met430Thr)	ANKAR (M430T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2651760	NM_001378068.1(ANKAR):c.1298A>G (p.His433Arg)	ANKAR (H433R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 775796	NM_001378068.1(ANKAR):c.1307+5G>A	ANKAR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 785983	NM_001378068.1(ANKAR):c.1313A>C (p.Tyr438Ser)	ANKAR (Y438S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 742027	NM_001378068.1(ANKAR):c.1332A>G (p.Leu444=)	ANKAR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2570043	NM_001378068.1(ANKAR):c.1367G>C (p.Trp456Ser)	ANKAR (W456S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295503	NM_001378068.1(ANKAR):c.1394A>G (p.Asn465Ser)	ANKAR (N465S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613209	NM_001378068.1(ANKAR):c.1501G>A (p.Gly501Ser)	ANKAR (G501S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295653	NM_001378068.1(ANKAR):c.1554C>G (p.Ser518Arg)	ANKAR (S518R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355772	NM_001378068.1(ANKAR):c.1555C>T (p.Arg519Cys)	ANKAR (R519C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619484	NM_001378068.1(ANKAR):c.1603A>C (p.Thr535Pro)	ANKAR (T535P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 727247	NM_001378068.1(ANKAR):c.1616A>T (p.His539Leu)	ANKAR (H539L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2558871	NM_001378068.1(ANKAR):c.1675G>A (p.Val559Ile)	ANKAR (V559I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600607	NM_001378068.1(ANKAR):c.1688G>A (p.Arg563His)	ANKAR (R563H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402942	NM_001378068.1(ANKAR):c.1723C>T (p.His575Tyr)	ANKAR (H575Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295483	NM_001378068.1(ANKAR):c.1738G>T (p.Ala580Ser)	ANKAR (A580S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323472	NM_001378068.1(ANKAR):c.1738G>A (p.Ala580Thr)	ANKAR (A580T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120198	NM_001378068.1(ANKAR):c.1772G>A (p.Cys591Tyr)	ANKAR (C591Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295664	NM_001378068.1(ANKAR):c.1790C>T (p.Thr597Met)	ANKAR (T597M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605116	NM_001378068.1(ANKAR):c.1808G>T (p.Gly603Val)	ANKAR (G603V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237086	NM_001378068.1(ANKAR):c.1819A>G (p.Ile607Val)	ANKAR (I607V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2651761	NM_001378068.1(ANKAR):c.1830C>T (p.Ala610=)	ANKAR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2230439	NM_001378068.1(ANKAR):c.1846G>A (p.Val616Ile)	ANKAR (V616I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2518943	NM_001378068.1(ANKAR):c.1978T>C (p.Ser660Pro)	ANKAR (S660P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234649	NM_001378068.1(ANKAR):c.2014G>C (p.Gly672Arg)	ANKAR (G672R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120217	NM_001378068.1(ANKAR):c.2041T>A (p.Leu681Ile)	ANKAR (L681I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783346	NM_001378068.1(ANKAR):c.2044A>G (p.Thr682Ala)	ANKAR (T682A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2373772	NM_001378068.1(ANKAR):c.2120A>C (p.Glu707Ala)	ANKAR (E707A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295474	NM_001378068.1(ANKAR):c.2147G>A (p.Arg716Gln)	ANKAR (R716Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395028	NM_001378068.1(ANKAR):c.2161G>A (p.Val721Ile)	ANKAR (V721I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345369	NM_001378068.1(ANKAR):c.2164A>G (p.Met722Val)	ANKAR (M722V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120231	NM_001378068.1(ANKAR):c.2324C>A (p.Ala775Glu)	ANKAR (A775E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 714134	NM_001378068.1(ANKAR):c.2327T>C (p.Val776Ala)	ANKAR (V776A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 785984	NM_001378068.1(ANKAR):c.2337G>A (p.Leu779=)	ANKAR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2321739	NM_001378068.1(ANKAR):c.2344G>A (p.Ala782Thr)	ANKAR (A782T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622307	NM_001378068.1(ANKAR):c.2423A>G (p.Tyr808Cys)	ANKAR (Y808C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295623	NM_001378068.1(ANKAR):c.2453T>C (p.Val818Ala)	ANKAR (V818A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295538	NM_001378068.1(ANKAR):c.2537G>A (p.Cys846Tyr)	ANKAR (C846Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295519	NM_001378068.1(ANKAR):c.2542C>T (p.Arg848Trp)	ANKAR (R848W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120236	NM_001378068.1(ANKAR):c.2564A>T (p.Glu855Val)	ANKAR (E855V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609983	NM_001378068.1(ANKAR):c.2570A>C (p.Asn857Thr)	ANKAR (N857T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591259	NM_001378068.1(ANKAR):c.2593A>C (p.Lys865Gln)	ANKAR (K865Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394145	NM_001378068.1(ANKAR):c.2608C>A (p.Leu870Ile)	ANKAR (L870I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301647	NM_001378068.1(ANKAR):c.2615G>T (p.Arg872Ile)	ANKAR (R872I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543314	NM_001378068.1(ANKAR):c.2681G>C (p.Arg894Pro)	ANKAR (R894P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248635	NM_001378068.1(ANKAR):c.2726T>G (p.Ile909Ser)	ANKAR (I909S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465322	NM_001378068.1(ANKAR):c.2753G>A (p.Gly918Glu)	ANKAR (G918E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120249	NM_001378068.1(ANKAR):c.2810A>T (p.His937Leu)	ANKAR (H937L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781687	NM_001378068.1(ANKAR):c.2814C>T (p.Asn938=)	ANKAR	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3295603	NM_001378068.1(ANKAR):c.2875A>G (p.Lys959Glu)	ANKAR (K959E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120253	NM_001378068.1(ANKAR):c.2904A>T (p.Gln968His)	ANKAR (Q968H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551924	NM_001378068.1(ANKAR):c.2965G>C (p.Glu989Gln)	ANKAR (E989Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120256	NM_001378068.1(ANKAR):c.2975G>A (p.Gly992Glu)	ANKAR (G992E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314544	NM_001378068.1(ANKAR):c.3137C>T (p.Thr1046Met)	ANKAR (T1046M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530032	NM_001378068.1(ANKAR):c.3191T>C (p.Ile1064Thr)	ANKAR (I1064T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295644	NM_001378068.1(ANKAR):c.3214C>G (p.Pro1072Ala)	ANKAR (P1072A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120259	NM_001378068.1(ANKAR):c.3325T>C (p.Cys1109Arg)	ANKAR (C1109R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226765	NM_001378068.1(ANKAR):c.3364C>T (p.His1122Tyr)	ANKAR (H1122Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257510	NM_001378068.1(ANKAR):c.3419A>G (p.Glu1140Gly)	ANKAR (E1140G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120265	NM_001378068.1(ANKAR):c.3425A>T (p.Asp1142Val)	ANKAR (D1142V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604046	NM_001378068.1(ANKAR):c.3476G>A (p.Arg1159His)	ANKAR (R1159H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120271	NM_001378068.1(ANKAR):c.3539T>G (p.Leu1180Arg)	ANKAR (L1180R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295647	NM_001378068.1(ANKAR):c.3653T>C (p.Leu1218Ser)	ANKAR (L1218S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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