ClinVar for Gene (Select 254528) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294174	NM_001163560.3(MEIOB):c.760A>G (p.Ile254Val)	MEIOB (I254V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294173	NM_001163560.3(MEIOB):c.941A>G (p.Glu314Gly)	MEIOB (E314G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294172	NM_001163560.3(MEIOB):c.791C>G (p.Ala264Gly)	MEIOB (A264G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243525	NC_000016.9:g.(?_1822222)_(2550959_?)dup	ABCA3, BRICD5 +39 more	Duplication	Caused by mutation in the TBC1 domain family, member 24 +2 more	GUncertain significance
Select item 3243466	NC_000016.9:g.(?_1607916)_(2130398_?)dup	CRAMP1, EME2 +27 more	Duplication	Tuberous sclerosis 2	GUncertain significance
Select item 3243222	NC_000016.9:g.(?_339420)_(3767509_?)dup	ABCA3, AMDHD2 +142 more	Duplication	Idiopathic generalized epilepsy +2 more	GUncertain significance
Select item 3125272	NM_001163560.3(MEIOB):c.742A>C (p.Thr248Pro)	MEIOB (T248P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125271	NM_001163560.3(MEIOB):c.717C>G (p.Asp239Glu)	MEIOB (D239E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125269	NM_001163560.3(MEIOB):c.662G>A (p.Ser221Asn)	MEIOB (S221N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125268	NM_001163560.3(MEIOB):c.610T>C (p.Ser204Pro)	MEIOB (S204P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125267	NM_001163560.3(MEIOB):c.572G>A (p.Gly191Asp)	MEIOB (G191D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125266	NM_001163560.3(MEIOB):c.556T>A (p.Ser186Thr)	MEIOB (S186T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125265	NM_001163560.3(MEIOB):c.445G>T (p.Asp149Tyr)	MEIOB (D149Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125264	NM_001163560.3(MEIOB):c.367A>G (p.Thr123Ala)	MEIOB (T123A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125263	NM_001163560.3(MEIOB):c.1407A>C (p.Lys469Asn)	FAHD1, MEIOB (K469N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125262	NM_001163560.3(MEIOB):c.1309G>A (p.Val437Ile)	FAHD1, MEIOB (V437I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125261	NM_001163560.3(MEIOB):c.1295T>G (p.Ile432Ser)	FAHD1, MEIOB (I432S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3060968	NM_001163560.3(MEIOB):c.52A>C (p.Thr18Pro)	MEIOB (T18P)	Single nucleotide variant (missense variant)	MEIOB-related disorder	GBenign
Select item 3060040	NM_001163560.3(MEIOB):c.831G>A (p.Thr277=)	MEIOB	Single nucleotide variant (synonymous variant)	MEIOB-related disorder	GBenign
Select item 3058504	NM_001163560.3(MEIOB):c.69+4G>A	MEIOB	Single nucleotide variant (intron variant)	MEIOB-related disorder	GLikely benign
Select item 3056873	NM_001163560.3(MEIOB):c.224A>C (p.Lys75Thr)	MEIOB (K75T)	Single nucleotide variant (missense variant)	MEIOB-related disorder	GBenign
Select item 3053766	NM_001163560.3(MEIOB):c.34A>G (p.Thr12Ala)	MEIOB (T12A)	Single nucleotide variant (missense variant)	MEIOB-related disorder	GLikely benign
Select item 3034787	NM_001163560.3(MEIOB):c.683-3C>T	MEIOB	Single nucleotide variant (intron variant)	MEIOB-related disorder	GLikely benign
Select item 2691783	NM_001163560.3(MEIOB):c.528+3A>C	MEIOB	Single nucleotide variant (intron variant)	Spermatogenic failure 22	GPathogenic
Select item 2691781	NM_001163560.3(MEIOB):c.1072_1073del (p.Met358fs)	FAHD1, MEIOB (M358fs)	Deletion (frameshift variant +1 more)	Spermatogenic failure 22 +1 more	GPathogenic
Select item 2691780	NM_001163560.3(MEIOB):c.683-1G>A	MEIOB	Single nucleotide variant (splice acceptor variant)	Premature ovarian failure 23 +1 more	GPathogenic
Select item 2691779	NM_001163560.3(MEIOB):c.1218G>A (p.Thr406=)	FAHD1, MEIOB	Single nucleotide variant (synonymous variant +1 more)	Premature ovarian failure 23	GPathogenic
Select item 2691778	NM_001163560.3(MEIOB):c.976G>A (p.Ala326Thr)	MEIOB (A326T)	Single nucleotide variant (missense variant)	Spermatogenic failure 22	GPathogenic
Select item 2684773	GRCh37/hg19 16p13.3(chr16:1505227-1960381)x3	CLCN7, CRAMP1 +15 more	Copy number gain	not provided	GUncertain significance
Select item 2684772	GRCh37/hg19 16p13.3(chr16:1054247-2592737)x3	ABCA3, AMDHD2 +66 more	Copy number gain	not provided	GLikely pathogenic
Select item 2610490	NM_001163560.3(MEIOB):c.1320C>A (p.His440Gln)	FAHD1, MEIOB (H411Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590143	NM_001163560.3(MEIOB):c.110G>C (p.Gly37Ala)	MEIOB (G37A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519241	NM_001163560.3(MEIOB):c.130A>G (p.Ile44Val)	MEIOB (I44V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512500	NM_001163560.3(MEIOB):c.1243G>A (p.Asp415Asn)	FAHD1, MEIOB (D415N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2498682	GRCh37/hg19 16p13.3(chr16:811896-2130379)x1	BAIAP3, C1QTNF8 +52 more	Copy number loss	not provided	GPathogenic
Select item 2492907	NM_001163560.3(MEIOB):c.1276C>A (p.Leu426Ile)	FAHD1, MEIOB (L426I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483307	NM_001163560.3(MEIOB):c.1309G>C (p.Val437Leu)	FAHD1, MEIOB (V408L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480777	NM_001163560.3(MEIOB):c.563G>A (p.Arg188Gln)	MEIOB (R188Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469764	NM_001163560.3(MEIOB):c.161C>T (p.Thr54Ile)	MEIOB (T54I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2426265	NC_000016.9:g.(?_256302)_(1918176_?)del	C1QTNF8, CACNA1H +67 more	Deletion	not provided	GUncertain significance
Select item 2425037	NC_000016.9:g.(?_256302)_(4852572_?)dup	TIGD7, TMEM204 +170 more	Duplication	Idiopathic generalized epilepsy +3 more	GUncertain significance
Select item 2399426	NM_001163560.3(MEIOB):c.152T>C (p.Phe51Ser)	MEIOB (F51S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363716	NM_001163560.3(MEIOB):c.1217C>T (p.Thr406Met)	FAHD1, MEIOB (T406M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352803	NM_001163560.3(MEIOB):c.1012A>C (p.Thr338Pro)	MEIOB (T338P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329358	NM_001163560.3(MEIOB):c.24G>T (p.Arg8Ser)	MEIOB (R8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302597	NM_001163560.3(MEIOB):c.784C>T (p.Pro262Ser)	MEIOB (P262S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296514	NM_001163560.3(MEIOB):c.92G>C (p.Gly31Ala)	MEIOB (G31A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255388	NM_001163560.3(MEIOB):c.430G>T (p.Val144Phe)	MEIOB (V144F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2081185	NM_001163560.3(MEIOB):c.1035-1G>A	FAHD1, MEIOB	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely pathogenic
Select item 2078114	NM_001163560.3(MEIOB):c.1207_1208del (p.Leu403fs)	MEIOB, FAHD1 (L403fs +1 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2045761	NM_001163560.3(MEIOB):c.814C>T (p.Arg272Ter)	MEIOB (R272*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1808452	GRCh37/hg19 16p13.3(chr16:1129080-2021055)x3	BAIAP3, C1QTNF8 +36 more	Copy number gain	not provided	GUncertain significance
Select item 1710928	GRCh37/hg19 16p13.3(chr16:111043-6627459)x3	ABCA3, ADCY9 +187 more	Copy number gain	See cases	GPathogenic
Select item 1526483	GRCh37/hg19 16p13.3(chr16:1847662-2653144)	ABCA3, AMDHD2 +38 more	Copy number gain	not specified	GUncertain significance
Select item 1340286	GRCh37/hg19 16p13.3(chr16:1830141-2592737)x3	ABCA3, AMDHD2 +41 more	Copy number gain	not provided	GUncertain significance
Select item 1328958	NM_001163560.3(MEIOB):c.1118_1121del (p.Phe373fs)	FAHD1, MEIOB (F373fs)	Deletion (frameshift variant +1 more)	Azoospermia	GPathogenic
Select item 1228722	NM_001163560.3(MEIOB):c.782T>C (p.Ile261Thr)	MEIOB (I261T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1180508	GRCh37/hg19 16p13.3(chr16:84485-5251013)x3	JPT2, KCTD5 +188 more	Copy number gain	not provided	GPathogenic
Select item 1017417	NC_000016.9:g.(?_624055)_(2153916_?)dup	CCDC78, ANTKMT +71 more	Duplication	Epilepsy +2 more	GUncertain significance
Select item 980573	GRCh37/hg19 16p13.3(chr16:85880-5249457)x3	ABCA3, ADCY9 +188 more	Copy number gain	not provided	GPathogenic
Select item 978603	NC_000016.10:g.1851807_2093151del	GFER, HS3ST6 +43 more	Deletion	Tuberous sclerosis 2	GPathogenic
Select item 833445	NC_000016.9:g.(?_1203718)_(2185710_?)del	EME2, FAHD1 +45 more	Deletion	Tuberous sclerosis 2	GPathogenic
Select item 833344	NC_000016.9:g.(?_624055)_(2550979_?)dup	IGFALS, MRPS34 +86 more	Duplication	Idiopathic generalized epilepsy +1 more	GUncertain significance
Select item 832709	NC_000016.9:g.(?_624055)_(2148005_?)del	CCDC78, CHTF18 +71 more	Deletion	Tuberous sclerosis 2	GPathogenic
Select item 831814	NC_000016.10:g.(?_1523498)_(2064447_?)del	MAPK8IP3, MEIOB +28 more	Deletion	Tuberous sclerosis 2	GPathogenic
Select item 791645	NM_001163560.3(MEIOB):c.634G>A (p.Asp212Asn)	MEIOB (D212N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 786285	NM_001163560.3(MEIOB):c.527C>T (p.Ser176Leu)	MEIOB (S176L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 715773	NM_001163560.3(MEIOB):c.1306-5C>T	FAHD1, MEIOB	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 711956	NM_001163560.3(MEIOB):c.952G>T (p.Asp318Tyr)	MEIOB (D318Y)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 689437	Single allele	CRAMP1, EME2 +28 more	Inversion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 688348	GRCh37/hg19 16p13.3(chr16:85880-2053328)x1	ANTKMT, ARHGDIG +89 more	Copy number loss	not provided	GPathogenic
Select item 685169	GRCh37/hg19 16p13.3(chr16:1727095-1947413)x3	CRAMP1, EME2 +10 more	Copy number gain	not provided	GUncertain significance
Select item 655214	NC_000016.9:g.(?_624055)_(2115656_?)del	ANTKMT, BAIAP3 +69 more	Deletion	Tuberous sclerosis 2	GPathogenic
Select item 625723	GRCh37/hg19 16p13.3(chr16:109978-4316797)	ABCA3, ADCY9 +159 more	Copy number gain	Chromosome 16p13.3 duplication syndrome	GPathogenic
Select item 564257	GRCh37/hg19 16p13.3(chr16:1734363-2285561)x1	BRICD5, CASKIN1 +34 more	Copy number loss	not provided	GPathogenic
Select item 564256	GRCh37/hg19 16p13.3(chr16:1505184-4415346)x3	ABCA3, ADCY9 +103 more	Copy number gain	not provided	GPathogenic
Select item 564254	GRCh37/hg19 16p13.3-13.13(chr16:85880-11209288)x3	ABAT, ABCA3 +206 more	Copy number gain	not provided	GPathogenic
Select item 564253	GRCh37/hg19 16p13.3(chr16:85880-3216551)x3	ABCA3, AMDHD2 +139 more	Copy number gain	not provided	GPathogenic
Select item 443477	GRCh37/hg19 16p13.3-13.2(chr16:85880-9883129)x3	ABAT, ABCA3 +198 more	Copy number gain	See cases	GPathogenic
Select item 443183	GRCh37/hg19 16p13.3-12.2(chr16:85880-22442007)x3	ABAT, ABCA3 +295 more	Copy number gain	See cases	GPathogenic
Select item 443121	GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	AARS1, ABAT +811 more	Copy number gain	See cases	GPathogenic
Select item 443120	GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	CCL22, CCNF +811 more	Copy number gain	See cases	GPathogenic
Select item 442872	GRCh37/hg19 16p13.3-12.3(chr16:85880-19806921)x3	PRSS27, PRSS33 +263 more	Copy number gain	See cases	GPathogenic
Select item 441740	GRCh37/hg19 16p13.3(chr16:643377-3125125)x3	ABCA3, AMDHD2 +111 more	Copy number gain	See cases	GUncertain significance
Select item 440759	NM_001163560.3(MEIOB):c.191A>T (p.Asn64Ile)	MEIOB (N64I)	Single nucleotide variant (missense variant)	Spermatogenic failure 22	GPathogenic
Select item 395719	GRCh37/hg19 16p13.3-13.2(chr16:78801-9169448)	CLDN6, CLDN9 +196 more	Copy number gain	See cases	GPathogenic
Select item 395502	GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	ABCC6, BCL7C +811 more	Copy number gain	See cases	GPathogenic
Select item 394840	GRCh37/hg19 16p13.3(chr16:97133-5122974)x3	ABCA3, ADCY9 +187 more	Copy number gain	See cases	GPathogenic
Select item 375693	maternal UPD(16p)	ALG1, BICDL2 +388 more	Complex	Hemimegalencephaly	GPathogenic
Select item 253874	GRCh37/hg19 16p13.3(chr16:1860861-2070554)x3	MEIOB, FAHD1 +14 more	Copy number gain	See cases	GUncertain significance
Select item 221511	GRCh37/hg19 16p13.3-12.3(chr16:1274615-19073133)x3	AMDHD2, ANKS3 +202 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance
Select item 221391	GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3	ABAT, ABCA3 +384 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance
Select item 219021	GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3	ABAT, ABCA3 +330 more	Copy number gain	See cases	GPathogenic
Select item 155643	GRCh38/hg38 16p13.3-13.11(chr16:666662-15743104)x3	ABAT, ABCA3 +926 more	Copy number gain	See cases	GPathogenic
Select item 150284	GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3	EEF2KMT, ELOB +917 more	Copy number gain	See cases	GPathogenic
Select item 148760	GRCh38/hg38 16p13.3(chr16:46722-1867327)x1	ANTKMT, ARHGDIG +224 more	Copy number loss	See cases	GPathogenic
Select item 147509	GRCh38/hg38 16p13.3(chr16:46766-4247185)x3	LOC125146383, LOC125146384 +556 more	Copy number gain	See cases	GPathogenic
Select item 146395	GRCh38/hg38 16p13.3(chr16:1850978-2116369)x3	GFER, HS3ST6 +44 more	Copy number gain	See cases	GUncertain significance
Select item 144298	GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3	ABAT, ABCA3 +843 more	Copy number gain	See cases	GPathogenic
Select item 59411	GRCh38/hg38 16p13.3(chr16:46766-1997582)x1	ANTKMT, ARHGDIG +253 more	Copy number loss	See cases	GPathogenic

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