List of variants in gene CEMIP reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_001293298.2(CEMIP):c.1971G>A (p.Pro657=)	rs1553647	0.99016
NM_001293298.2(CEMIP):c.3699+63C>G	rs1553646	0.98529
NM_001293298.2(CEMIP):c.2289-117C>T	rs2271163	0.81390
NM_001293298.2(CEMIP):c.869-61G>A	rs8028511	0.42428
NM_001293298.2(CEMIP):c.1587+57A>G	rs2271164	0.37371
NM_001293298.2(CEMIP):c.2420+210T>C	rs11072963	0.34960
NM_001293298.2(CEMIP):c.2420+195A>G	rs12441164	0.34078
NM_001293298.2(CEMIP):c.797+26C>G	rs35343835	0.31308
NM_001293298.2(CEMIP):c.798-159G>A	rs11631636	0.29547
NM_001293298.2(CEMIP):c.242-267G>C	rs10152744	0.28787
NM_001293298.2(CEMIP):c.798-109G>T	rs2271159	0.27383
NM_001293298.2(CEMIP):c.94+168G>A	rs7174325	0.27088
NM_001293298.2(CEMIP):c.2202+133A>C	rs2271162	0.18849
NM_001293298.2(CEMIP):c.381-263C>T	rs9673075	0.16324
NM_001293298.2(CEMIP):c.1884T>C (p.Cys628=)	rs2271160	0.13852
NM_001293298.2(CEMIP):c.3222-225G>A	rs8026419	0.11991
NM_001293298.2(CEMIP):c.2203-143G>T	rs55811683	0.11804
NM_001293298.2(CEMIP):c.249G>A (p.Leu83=)	rs35541581	0.06893
NM_001293298.2(CEMIP):c.1412-76G>A	rs28452628	0.04085
NM_001293298.2(CEMIP):c.964+256C>T	rs76868414	0.04028
NM_001293298.2(CEMIP):c.95-131G>A	rs73501087	0.03754
NM_001293298.2(CEMIP):c.3222-185T>C	rs76023943	0.02190
NM_001293298.2(CEMIP):c.798-87C>T	rs74030631	0.02144
NM_001293298.2(CEMIP):c.2074-72G>A	rs7165406	0.02104
NM_001293298.2(CEMIP):c.1086+82T>A	rs117978356	0.02006
NM_001293298.2(CEMIP):c.1797+102T>C	rs73500487	0.01847
NM_001293298.2(CEMIP):c.3699+156C>T	rs73507416	0.01820
NM_001293298.2(CEMIP):c.242-144A>G	rs77041747	0.01819
NM_001293298.2(CEMIP):c.381-273A>G	rs112450705	0.01783
NM_001293298.2(CEMIP):c.1587+79G>A	rs115865339	0.01565
NM_001293298.2(CEMIP):c.2348A>G (p.His783Arg)	rs12441101	0.00694
NM_001293298.2(CEMIP):c.1087-239G>A	rs16972538
NM_001293298.2(CEMIP):c.1587+182del	rs71153559
NM_001293298.2(CEMIP):c.1798-267del	rs11300537
NM_001293298.2(CEMIP):c.3221+208C>T	rs77336371
NM_001293298.2(CEMIP):c.94+78G>C	rs28394231

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