ClinVar Miner

List of variants in gene CDH23 reported as benign for not provided

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Gene type:
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Total variants: 46
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HGVS dbSNP
GRCh37/hg19 10q22.1(chr10:73129458-73162237)x1
GRCh37/hg19 10q22.1(chr10:73141020-73157945)x1
GRCh37/hg19 10q22.1(chr10:73154073-73157945)x1
NC_000010.11:g.71511238A>G
NC_000010.11:g.71679344T>C
NC_000010.11:g.71695551T>C
NC_000010.11:g.71739804C>G
NC_000010.11:g.71784847T>C
NC_000010.11:g.71799470C>T
NM_022124.6(CDH23):c.-5-251A>G
NM_022124.6(CDH23):c.-5-83C>A
NM_022124.6(CDH23):c.1053C>T (p.Ser351=) rs7903475
NM_022124.6(CDH23):c.1134+164C>G
NM_022124.6(CDH23):c.1135-128A>G
NM_022124.6(CDH23):c.1290+217T>C
NM_022124.6(CDH23):c.1307G>A (p.Ser436Asn) rs111033369
NM_022124.6(CDH23):c.145+135C>T
NM_022124.6(CDH23):c.146-125T>C
NM_022124.6(CDH23):c.1515-193A>G
NM_022124.6(CDH23):c.1515-341T>A
NM_022124.6(CDH23):c.1752+110T>C
NM_022124.6(CDH23):c.1753-78A>T
NM_022124.6(CDH23):c.2059+79C>T
NM_022124.6(CDH23):c.2289+135C>T
NM_022124.6(CDH23):c.2289+240T>C
NM_022124.6(CDH23):c.2290-240C>G
NM_022124.6(CDH23):c.2290-267C>T
NM_022124.6(CDH23):c.2290-268G>A
NM_022124.6(CDH23):c.2953+146C>T
NM_022124.6(CDH23):c.4341T>C (p.Asp1447=) rs12218564
NM_022124.6(CDH23):c.4359+240A>G
NM_022124.6(CDH23):c.4360-333T>C
NM_022124.6(CDH23):c.4488+298G>A
NM_022124.6(CDH23):c.4617+154C>T
NM_022124.6(CDH23):c.4618-77C>T
NM_022124.6(CDH23):c.4846-135C>T
NM_022124.6(CDH23):c.5187+73C>T
NM_022124.6(CDH23):c.5297T>C (p.Phe1766Ser) rs114745089
NM_022124.6(CDH23):c.5821-309G>A
NM_022124.6(CDH23):c.6197G>A (p.Arg2066Gln) rs201887949
NM_022124.6(CDH23):c.6596T>A (p.Ile2199Asn) rs111033494
NM_022124.6(CDH23):c.6830-81G>A
NM_022124.6(CDH23):c.754-254T>C
NM_022124.6(CDH23):c.7C>T (p.Arg3Cys) rs7902757
NM_022124.6(CDH23):c.8808C>T (p.Asp2936=) rs148743086
NM_022124.6(CDH23):c.9320-93C>G

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