ClinVar for Gene (Select 4205) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3891653	NM_001319206.4(MEF2A):c.1293ACC[1] (p.Pro433del)	MEF2A (P157del +13 more)	Microsatellite (inframe_deletion)	Coronary artery disease, autosomal dominant, 1	GUncertain significance
Select item 3891652	NM_001319206.4(MEF2A):c.1253AGC[5] (p.Gln423_Gln428del)	MEF2A	Microsatellite (inframe_deletion)	Coronary artery disease, autosomal dominant, 1	GUncertain significance
Select item 3872090	NM_001319206.4(MEF2A):c.1504G>A (p.Ala502Thr)	MEF2A (A226T +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3872089	NM_001319206.4(MEF2A):c.993G>A (p.Pro331=)	MEF2A	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3770847	NM_001319206.4(MEF2A):c.1311_1331del (p.Gln438_Pro444del)	MEF2A	Deletion	not provided	GBenign
Select item 3394723	NM_001319206.4(MEF2A):c.565G>A (p.Val189Met)	MEF2A (V189M +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3394722	NM_001319206.4(MEF2A):c.512C>T (p.Thr171Met)	MEF2A (T103M +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3394721	NM_001319206.4(MEF2A):c.599C>T (p.Thr200Ile)	MEF2A (T202I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3394720	NM_001319206.4(MEF2A):c.1292C>A (p.Pro431Gln)	MEF2A (P155Q +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3394719	NM_001319206.4(MEF2A):c.751A>T (p.Thr251Ser)	MEF2A (T185S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3391927	GRCh37/hg19 15q26.1-26.3(chr15:93918298-102429112)x1	ADAMTS17, ALDH1A3 +23 more	Copy number loss	not provided	GPathogenic
Select item 3294086	NM_001319206.4(MEF2A):c.149G>C (p.Ser50Thr)	MEF2A (S50T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294085	NM_001319206.4(MEF2A):c.562A>C (p.Asn188His)	MEF2A (N190H +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294084	NM_001319206.4(MEF2A):c.232A>G (p.Ser78Gly)	MEF2A (S78G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3250510	NM_001319206.4(MEF2A):c.1284GCC[2] (p.Pro433del)	MEF2A (P157del +13 more)	Microsatellite (inframe_deletion)	not provided	GLikely benign
Select item 3242325	GRCh37/hg19 15q26.3(chr15:98615561-102400033)x1	MEF2A, SNRPA1 +19 more	Copy number loss	not provided	GPathogenic
Select item 3125104	NM_001319206.4(MEF2A):c.1439T>C (p.Val480Ala)	MEF2A (V474A +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125103	NM_001319206.4(MEF2A):c.1289C>T (p.Pro430Leu)	MEF2A (P356L +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125102	NM_001319206.4(MEF2A):c.1127G>A (p.Ser376Asn)	MEF2A (S263N +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3064723	NM_001319206.4(MEF2A):c.407A>G (p.Gln136Arg)	MEF2A (Q136R +6 more)	Single nucleotide variant (missense variant +1 more)	Coronary artery disease, autosomal dominant, 1	GUncertain significance
Select item 3063384	GRCh37/hg19 15q26.1-26.3(chr15:94176550-102429112)x3	ADAMTS17, ALDH1A3 +23 more	Copy number gain	not specified	GPathogenic
Select item 3063383	GRCh37/hg19 15q26.2-26.3(chr15:94300072-101810099)x1	ADAMTS17, ALDH1A3 +16 more	Copy number loss	not specified	GPathogenic
Select item 3063364	GRCh37/hg19 15q26.3(chr15:98679543-102429112)x1	ADAMTS17, ALDH1A3 +19 more	Copy number loss	not specified	GPathogenic
Select item 3059607	NM_001319206.4(MEF2A):c.891G>A (p.Gln297=)	MEF2A	Single nucleotide variant (synonymous variant +1 more)	MEF2A-related disorder	GBenign
Select item 3059085	NM_001319206.4(MEF2A):c.1347G>T (p.Gly449=)	MEF2A	Single nucleotide variant (synonymous variant)	MEF2A-related disorder	GBenign
Select item 3058865	NM_001319206.4(MEF2A):c.885T>C (p.Asn295=)	MEF2A	Single nucleotide variant (synonymous variant +1 more)	MEF2A-related disorder	GBenign
Select item 3056661	NM_001319206.4(MEF2A):c.1434A>G (p.Pro478=)	MEF2A	Single nucleotide variant (synonymous variant)	MEF2A-related disorder	GBenign
Select item 3056101	NM_001319206.4(MEF2A):c.1245G>A (p.Ser415=)	MEF2A	Single nucleotide variant (synonymous variant)	MEF2A-related disorder	GBenign
Select item 3044407	NM_001319206.4(MEF2A):c.1286C>A (p.Pro429Gln)	MEF2A (P153Q +13 more)	Single nucleotide variant (missense variant)	MEF2A-related disorder	GLikely benign
Select item 3043823	NM_001319206.4(MEF2A):c.1137T>C (p.Val379=)	MEF2A	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3041576	NM_001319206.4(MEF2A):c.611-8G>A	MEF2A	Single nucleotide variant (intron variant)	MEF2A-related disorder	GBenign
Select item 3039553	NM_001319206.4(MEF2A):c.1253AGC[6] (p.Gln424_Gln428del)	MEF2A	Microsatellite	MEF2A-related disorder	GBenign
Select item 2671598	Single allele	ADAMTS17, MEF2A +19 more	Deletion	not provided	GPathogenic
Select item 2614361	NM_001319206.4(MEF2A):c.1112G>C (p.Gly371Ala)	MEF2A (G297A +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609090	NM_001319206.4(MEF2A):c.1231C>T (p.Arg411Cys)	MEF2A (R403C +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600075	NM_001319206.4(MEF2A):c.1490G>A (p.Arg497Gln)	MEF2A (R384Q +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2580298	GRCh37/hg19 15q24.1-26.3(chr15:75165490-102520892)x3	ABHD17C, ABHD2 +174 more	Copy number gain	See cases	GPathogenic
Select item 2572375	GRCh37/hg19 15q26.3(chr15:99021824-101196161)x1	ADAMTS17, ASB7 +9 more	Copy number loss	See cases	GPathogenic
Select item 2547042	NM_001319206.4(MEF2A):c.916C>G (p.Gln306Glu)	MEF2A (Q186E +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538288	NM_001319206.4(MEF2A):c.662G>A (p.Ser221Asn)	MEF2A (S153N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527803	NM_001319206.4(MEF2A):c.722G>A (p.Gly241Asp)	MEF2A (G129D +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2498631	GRCh37/hg19 15q25.2-26.3(chr15:84228005-102264590)x3	ABHD2, ACAN +86 more	Copy number gain	not provided	GPathogenic
Select item 2465526	NM_001319206.4(MEF2A):c.1297C>T (p.Pro433Ser)	MEF2A (P313S +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391955	NM_001319206.4(MEF2A):c.403C>T (p.Pro135Ser)	MEF2A (P69S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379604	NM_001319206.4(MEF2A):c.647A>G (p.Asn216Ser)	MEF2A (N148S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318812	NM_001319206.4(MEF2A):c.947C>T (p.Thr316Ile)	MEF2A (T196I +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314675	NM_001319206.4(MEF2A):c.1289C>A (p.Pro430Gln)	MEF2A (P310Q +13 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2296347	NM_001319206.4(MEF2A):c.427A>C (p.Thr143Pro)	MEF2A (T75P +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271747	NM_001319206.4(MEF2A):c.1101G>C (p.Gln367His)	MEF2A (Q299H +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264622	NM_001319206.4(MEF2A):c.1058C>T (p.Ser353Leu)	MEF2A (S233L +13 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243622	NM_001319206.4(MEF2A):c.623G>A (p.Ser208Asn)	MEF2A (S208N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1809424	GRCh37/hg19 15q24.3-26.3(chr15:77512817-102035027)x3	ABHD17C, ABHD2 +139 more	Copy number gain	not provided	GPathogenic
Select item 1808231	GRCh37/hg19 15q26.3(chr15:99772763-100195207)x3	LRRC28, MEF2A +1 more	Copy number gain	not provided	GUncertain significance
Select item 1807891	GRCh37/hg19 15q26.3(chr15:99507922-100153799)x3	LRRC28, MEF2A +3 more	Copy number gain	not provided	GUncertain significance
Select item 1526478	GRCh37/hg19 15q26.3(chr15:99682151-100147153)	LRRC28, MEF2A +1 more	Copy number gain	not specified	GUncertain significance
Select item 1526475	GRCh37/hg19 15q26.3(chr15:99258367-102429112)	LYSMD4, MEF2A +19 more	Copy number loss	not specified	GPathogenic
Select item 1526472	GRCh37/hg19 15q26.2-26.3(chr15:97223728-102429112)	ADAMTS17, ALDH1A3 +21 more	Copy number loss	not specified	GPathogenic
Select item 1526471	GRCh37/hg19 15q26.2-26.3(chr15:97026327-102429112)	ADAMTS17, ALDH1A3 +21 more	Copy number loss	not specified	GPathogenic
Select item 1526470	GRCh37/hg19 15q26.2-26.3(chr15:94836128-101302111)	ADAMTS17, ARRDC4 +13 more	Copy number loss	not specified	GPathogenic
Select item 1448913	NC_000015.9:g.(?_98947180)_(101791661_?)dup	LYSMD4, MEF2A +12 more	Duplication	not provided	GUncertain significance
Select item 1180505	GRCh37/hg19 15q26.1-26.3(chr15:92335751-102399741)x1	ADAMTS17, ALDH1A3 +29 more	Copy number loss	not provided	GPathogenic
Select item 1077189	Single allele	ADAMTS17, MEF2A +12 more	Deletion	Chromosome 15q26-qter deletion syndrome	GLikely pathogenic
Select item 1049163	NM_001319206.4(MEF2A):c.123_124del (p.Cys41_Glu42delinsTer)	MEF2A	Microsatellite (nonsense +1 more)	not provided	GUncertain significance
Select item 983158	GRCh37/hg19 15q25.3-26.3(chr15:86962053-102531392)x1	ABHD2, ACAN +77 more	Copy number loss	See cases	GPathogenic
Select item 980651	GRCh37/hg19 15q26.3(chr15:99508457-100415587)x3	PGPEP1L, SYNM +4 more	Copy number gain	not provided	GUncertain significance
Select item 980643	GRCh37/hg19 15q26.2-26.3(chr15:98275761-102358202)x1	PCSK6, PGPEP1L +19 more	Copy number loss	not provided	GPathogenic
Select item 815762	GRCh37/hg19 15q26.3(chr15:100249056-100901315)x3	ADAMTS17, LYSMD4 +1 more	Copy number gain	not provided	GLikely benign
Select item 815756	GRCh37/hg19 15q26.3(chr15:98806822-100262828)x3	PGPEP1L, MEF2A +4 more	Copy number gain	not provided	GUncertain significance
Select item 815755	GRCh37/hg19 15q26.3(chr15:98795669-102429112)x1	ADAMTS17, ALDH1A3 +19 more	Copy number loss	not provided	GPathogenic
Select item 815754	GRCh37/hg19 15q26.3(chr15:98686212-102429112)x1	ADAMTS17, ALDH1A3 +19 more	Copy number loss	not provided	GPathogenic
Select item 815743	GRCh37/hg19 15q25.3-26.3(chr15:87189245-102429112)x1	ABHD2, ACAN +76 more	Copy number loss	not provided	GPathogenic
Select item 805881	GRCh37/hg19 15q26.2-26.3(chr15:96878099-102397836)x1	MEF2A, NR2F2 +22 more	Copy number loss	Chromosome 15q26-qter deletion syndrome	GPathogenic
Select item 798876	NM_001319206.4(MEF2A):c.9G>A (p.Arg3=)	MEF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 779963	NM_001319206.4(MEF2A):c.1299G>A (p.Pro433=)	MEF2A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 779275	NM_001319206.4(MEF2A):c.1435A>G (p.Ile479Val)	MEF2A (I403V +10 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 778574	NM_001319206.4(MEF2A):c.1253AGC[13] (p.Gln427_Gln428dup)	MEF2A	Microsatellite (inframe_insertion)	not provided +1 more	GBenign
Select item 762680	NM_001319206.4(MEF2A):c.1074G>A (p.Ser358=)	MEF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 753730	NM_001319206.4(MEF2A):c.390+167G>A	MEF2A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 735182	NM_001319206.4(MEF2A):c.930C>T (p.Thr310=)	MEF2A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 688921	GRCh37/hg19 15q26.3(chr15:100176743-100330631)x1	LYSMD4, MEF2A	Copy number loss	not provided	GUncertain significance
Select item 688713	GRCh37/hg19 15q26.3(chr15:99880948-100441683)x3	LRRC28, LYSMD4 +1 more	Copy number gain	not provided	GUncertain significance
Select item 686177	GRCh37/hg19 15q26.1-26.3(chr15:90288175-102429112)x3	ADAMTS17, ALDH1A3 +54 more	Copy number gain	not provided	GPathogenic
Select item 625753	GRCh37/hg19 15q26.2-26.3(chr15:96873212-102389423)	ADAMTS17, ALDH1A3 +22 more	Copy number loss	not provided	GPathogenic
Select item 564237	GRCh37/hg19 15q26.3(chr15:99928623-102429112)x3	ADAMTS17, ALDH1A3 +14 more	Copy number gain	not provided	GLikely pathogenic
Select item 564235	GRCh37/hg19 15q26.3(chr15:99681869-100231283)x3	MEF2A, TTC23 +1 more	Copy number gain	not provided	GLikely benign
Select item 564234	GRCh37/hg19 15q26.3(chr15:99350059-100112556)x3	PGPEP1L, MEF2A +4 more	Copy number gain	not provided	GUncertain significance
Select item 564229	GRCh37/hg19 15q26.1-26.3(chr15:89743929-102429112)x3	ABHD2, ADAMTS17 +66 more	Copy number gain	not provided	GPathogenic
Select item 564221	GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3	ALPK3, AP3S2 +143 more	Copy number gain	not provided	GPathogenic
Select item 564214	GRCh37/hg19 15q23-26.3(chr15:71329220-102270758)x3	BBS4, BCL2A1 +214 more	Copy number gain	not provided	GPathogenic
Select item 560049	Single allele	ANKRD34C, ANKRD63 +521 more	Duplication	not provided	GPathogenic
Select item 443865	GRCh37/hg19 15q26.1-26.3(chr15:93148806-102429112)x3	ADAMTS17, ALDH1A3 +26 more	Copy number gain	See cases	GPathogenic
Select item 443651	GRCh37/hg19 15q26.3(chr15:98737093-102429112)x1	ADAMTS17, ALDH1A3 +19 more	Copy number loss	See cases	GPathogenic
Select item 443543	GRCh37/hg19 15q26.2-26.3(chr15:96913435-102429112)x1	ADAMTS17, ALDH1A3 +21 more	Copy number loss	See cases	GPathogenic
Select item 443542	GRCh37/hg19 15q26.2-26.3(chr15:95136822-102045577)x1	ADAMTS17, ALDH1A3 +18 more	Copy number loss	See cases	GPathogenic
Select item 443520	GRCh37/hg19 15q26.3(chr15:99928623-100441789)x3	LYSMD4, MEF2A	Copy number gain	See cases	GUncertain significance
Select item 443269	GRCh37/hg19 15q24.2-26.3(chr15:76061144-102429112)x3	OR4F15, OR4F6 +153 more	Copy number gain	See cases	GPathogenic
Select item 442893	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	AAGAB, ABHD17C +559 more	Copy number gain	See cases	GPathogenic
Select item 442892	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	EMC7, ENTREP2 +559 more	Copy number gain	See cases	GPathogenic
Select item 442426	GRCh37/hg19 15q26.2-26.3(chr15:98220018-102429112)x1	ADAMTS17, ALDH1A3 +20 more	Copy number loss	See cases	GPathogenic
Select item 403080	NM_001319206.4(MEF2A):c.1253AGC[9] (p.Gln427_Gln428del)	MEF2A	Microsatellite (inframe_deletion)	not specified	GBenign

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