ClinVar Miner

List of variants in gene CPT1A reported as benign for not provided

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001876.4(CPT1A):c.1353-47G>T rs3019576 0.92001
NM_001876.4(CPT1A):c.454-208C>T rs2924674 0.91736
NM_001876.4(CPT1A):c.1352+220A>G rs4261294 0.91564
NM_001876.4(CPT1A):c.1876-203G>A rs3019597 0.86196
NM_001876.4(CPT1A):c.1876-223G>C rs897048 0.75109
NM_001876.4(CPT1A):c.2142+93C>T rs3019598 0.35902
NC_000011.10:g.68754585G>A rs3018712 0.14685
NM_001876.4(CPT1A):c.880-134A>C rs3763830 0.13363
NM_001876.4(CPT1A):c.880-261T>C rs11228357 0.13329
NM_001876.4(CPT1A):c.281+310G>C rs2278906 0.12767
NM_001876.4(CPT1A):c.1741-28G>A rs2924699 0.12427
NM_001876.4(CPT1A):c.281+266G>A rs2278905 0.10048
NM_001876.4(CPT1A):c.694-272G>A rs7925592 0.08661
NM_001876.4(CPT1A):c.282-71C>T rs41302431 0.03751
NM_001876.4(CPT1A):c.555+156del rs60624953 0.03627
NM_001876.4(CPT1A):c.454-222G>C rs58382550 0.02493
NM_001876.4(CPT1A):c.454-162A>G rs58341713 0.02392
NM_001876.4(CPT1A):c.453+166A>C rs7108728 0.02165
NM_001876.4(CPT1A):c.282-236G>A rs148206888 0.00898
NM_001876.4(CPT1A):c.302C>T (p.Thr101Met) rs61731903 0.00262
NM_001876.4(CPT1A):c.1353-255C>T rs11228349
NM_001876.4(CPT1A):c.1741-89G>T rs7112615
NM_001876.4(CPT1A):c.1876-256dup rs5792450
NM_001876.4(CPT1A):c.2143-225GT[8] rs34518934
NM_001876.4(CPT1A):c.555+157_555+158del rs146360664
NM_001876.4(CPT1A):c.555+243ATTTT[11] rs59753299
NM_001876.4(CPT1A):c.555+243ATTTT[12] rs59753299
NM_001876.4(CPT1A):c.555+243ATTTT[6] rs59753299
NM_001876.4(CPT1A):c.555+243ATTTT[7] rs59753299
NM_001876.4(CPT1A):c.555+243ATTTT[8] rs59753299
NM_001876.4(CPT1A):c.693+34_693+35insAGCG rs371123694
NM_001876.4(CPT1A):c.693+36T>C rs61887063
NM_001876.4(CPT1A):c.693+37T>C rs61887062
NM_001876.4(CPT1A):c.771+80del rs141474465
NM_001876.4(CPT1A):c.967+243ATTT[5] rs10591978

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