MFSD4B[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150937	GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3	LOC129996876, LOC129996877 +1449 more	Copy number gain	See cases	GPathogenic
Select item 150641	GRCh38/hg38 6q16.1-22.31(chr6:96609994-122161548)x1	AFG1L, AK9 +558 more	Copy number loss	See cases	GPathogenic
Select item 155160	GRCh38/hg38 6q16.3-22.31(chr6:100054889-120488154)x1	LOC126859762, LOC126859763 +460 more	Copy number loss	See cases	GPathogenic
Select item 154178	GRCh38/hg38 6q16.3-21(chr6:103279465-113934239)x1	AFG1L, AK9 +297 more	Copy number loss	See cases	GPathogenic
Select item 153088	GRCh38/hg38 6q21-22.31(chr6:106503719-125781219)x1	AFG1L, AK9 +472 more	Copy number loss	See cases	GPathogenic
Select item 148944	GRCh38/hg38 6q21-22.1(chr6:107370141-115827482)x1	AFG1L, AK9 +224 more	Copy number loss	See cases	GPathogenic
Select item 57486	GRCh38/hg38 6q21-23.2(chr6:108944899-132067720)x1	AK9, AKAP7 +519 more	Copy number loss	See cases	GPathogenic
Select item 2233232	NM_153369.4(MFSD4B):c.239C>T (p.Pro80Leu)	MFSD4B (P80L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343839	NM_153369.4(MFSD4B):c.296T>C (p.Ile99Thr)	LOC123833521, MFSD4B (I99T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245678	NM_153369.4(MFSD4B):c.342G>T (p.Trp114Cys)	MFSD4B (W114C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391209	NM_153369.4(MFSD4B):c.784A>G (p.Met262Val)	MFSD4B (M262V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375198	NM_153369.4(MFSD4B):c.920C>T (p.Thr307Ile)	MFSD4B (T307I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325139	NM_153369.4(MFSD4B):c.958A>G (p.Ile320Val)	MFSD4B (I320V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3125799	NM_153369.4(MFSD4B):c.1348A>G (p.Asn450Asp)	MFSD4B (N450D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242312	GRCh37/hg19 6q21-22.31(chr6:109324789-124836619)x1	AK9, AMD1 +70 more	Copy number loss	not provided	GPathogenic
Select item 3062896	GRCh37/hg19 6q21-23.2(chr6:110546061-131896074)x3	AKAP7, AMD1 +87 more	Copy number gain	not specified	GLikely pathogenic
Select item 1808287	GRCh37/hg19 6q21(chr6:111198703-111878472)x3	AMD1, GTF3C6 +6 more	Copy number gain	not provided	GUncertain significance
Select item 1527277	GRCh37/hg19 6q21-22.1(chr6:110472732-114762836)	AMD1, CCN6 +21 more	Copy number loss	not specified	GUncertain significance
Select item 1527276	GRCh37/hg19 6q21(chr6:109564793-112223595)	AK9, AMD1 +21 more	Copy number loss	not specified	GUncertain significance
Select item 1527266	GRCh37/hg19 6q15-22.2(chr6:92054891-118329651)	AFG1L, AK9 +98 more	Copy number loss	not specified	GPathogenic
Select item 1527263	GRCh37/hg19 6q14.3-22.31(chr6:85988428-120548687)	AFG1L, AK9 +138 more	Copy number loss	not specified	GPathogenic
Select item 1048615	GRCh37/hg19 6q21(chr6:109796301-113083437)x3	AK9, AMD1 +22 more	Copy number gain	See cases	GUncertain significance
Select item 981211	GRCh37/hg19 6q16.1-21(chr6:98949950-114533905)x1	PREP, QRSL1 +66 more	Copy number loss	Deletion 6q16 q21	GPathogenic
Select item 974790	GRCh37/hg19 6q16.3-22.1(chr6:101296547-117004249)x3	DSE, FAM229B +69 more	Copy number gain	Microcephaly +1 more	GPathogenic
Select item 816620	GRCh37/hg19 6q21(chr6:109564694-112232351)x1	GPR6, METTL24 +21 more	Copy number loss	not provided	GUncertain significance
Select item 814864	GRCh37/hg19 6q21(chr6:111503087-111731131)x3	MFSD4B, SLC16A10 +1 more	Copy number gain	not provided	GUncertain significance
Select item 814863	GRCh37/hg19 6q21(chr6:111434909-111662102)x3	SLC16A10, REV3L +1 more	Copy number gain	not provided	GLikely benign
Select item 688010	GRCh37/hg19 6q21-22.31(chr6:110981075-119608396)x1	AMD1, ASF1A +45 more	Copy number loss	not provided	GPathogenic
Select item 685005	GRCh37/hg19 6q21(chr6:111437859-111765932)x3	MFSD4B, REV3L +1 more	Copy number gain	not provided	GUncertain significance
Select item 563220	GRCh37/hg19 6q21(chr6:111503087-111747187)x3	SLC16A10, REV3L +1 more	Copy number gain	not provided	GUncertain significance
Select item 563218	GRCh37/hg19 6q21(chr6:110419878-111698827)x1	SLC22A16, REV3L +10 more	Copy number loss	not provided	GUncertain significance
Select item 563204	GRCh37/hg19 6q16.1-22.1(chr6:95549951-116684929)x1	AFG1L, AK9 +80 more	Copy number loss	not provided	GPathogenic
Select item 443497	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	AARS2, ABCC10 +1028 more	Copy number gain	See cases	GPathogenic
Select item 443496	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	RING1, RIOK1 +1028 more	Copy number gain	See cases	GPathogenic

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Items: 34