ClinVar Miner

List of variants in gene JAM3 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_032801.5(JAM3):c.843-3T>C rs610382 0.47741
NM_032801.5(JAM3):c.*285G>A rs597320 0.47002
NM_032801.5(JAM3):c.256+57A>G rs646998 0.45380
NM_032801.5(JAM3):c.142+49T>C rs2276266 0.18125
NM_032801.5(JAM3):c.712+71T>C rs11223714 0.16285
NM_032801.5(JAM3):c.897+32G>A rs610829 0.11592
NM_032801.5(JAM3):c.612+265G>A rs11605753 0.07782
NM_032801.5(JAM3):c.257-153_257-152del rs145515548 0.07753
NM_032801.5(JAM3):c.898-61G>A rs12795060 0.07743
NM_032801.5(JAM3):c.142+231C>A rs12575294 0.07703
NM_032801.5(JAM3):c.76+253C>T rs144554045 0.06002
NM_032801.5(JAM3):c.898-150T>A rs539222462 0.03649
NC_000011.10:g.134068835C>G rs1940144 0.03189
NM_032801.5(JAM3):c.256+173T>C rs78860265 0.03113
NM_032801.5(JAM3):c.256+125_256+129del rs113932932 0.03101
NM_032801.5(JAM3):c.143-184G>T rs73600742 0.01834
NM_032801.5(JAM3):c.142+136G>A rs77508141 0.01709
NM_032801.5(JAM3):c.449T>C (p.Val150Ala) rs79915781 0.00973
NM_032801.5(JAM3):c.285G>A (p.Leu95=) rs148009046 0.00602
NM_032801.5(JAM3):c.921G>A (p.Ser307=) rs144672452 0.00182
NM_032801.5(JAM3):c.843-11T>G rs142616737 0.00143
NM_032801.5(JAM3):c.143-8C>T rs202130887 0.00044
NM_032801.5(JAM3):c.612+8C>A rs78756248 0.00033
NM_032801.5(JAM3):c.771C>T (p.Ala257=) rs201770276 0.00007
NM_032801.5(JAM3):c.*36G>T rs55689702
NM_032801.5(JAM3):c.142+91del rs141381598
NM_032801.5(JAM3):c.256+128del rs370582772
NM_032801.5(JAM3):c.410-14_410-13insCT rs3216140
NM_032801.5(JAM3):c.410-14_410-13insCTT rs3216140
NM_032801.5(JAM3):c.410-5dup
NM_032801.5(JAM3):c.612+159_612+162del rs71993546
NM_032801.5(JAM3):c.897+137_897+138insCAC rs1565508064
NM_032801.5(JAM3):c.897+137_897+138insCACAC rs1565508064
NM_032801.5(JAM3):c.897+138AC[18] rs368934602
NM_032801.5(JAM3):c.897+138AC[19] rs368934602
NM_032801.5(JAM3):c.897+138AC[22] rs368934602
NM_032801.5(JAM3):c.897+138AC[23] rs368934602
NM_032801.5(JAM3):c.898-21_898-18del rs139822951

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