List of variants in gene CDH23, PSAP studied for auditory system disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 34

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HGVS	dbSNP
NM_002778.4(PSAP):c.*238G>C
NM_002778.4(PSAP):c.*891G>A	rs7869
NM_002778.4(PSAP):c.1350+5G>A	rs11000016
NM_022124.6(CDH23):c.*104G>C	rs377312107
NM_022124.6(CDH23):c.*141G>A	rs535544696
NM_022124.6(CDH23):c.*204A>G	rs2290022
NM_022124.6(CDH23):c.*349A>G	rs1867978
NM_022124.6(CDH23):c.*361C>A	rs115033851
NM_022124.6(CDH23):c.*430A>T	rs562268606
NM_022124.6(CDH23):c.*434G>A	rs529522213
NM_022124.6(CDH23):c.*439C>T	rs140312023
NM_022124.6(CDH23):c.*478G>C	rs564392413
NM_022124.6(CDH23):c.*510G>A	rs1054635
NM_022124.6(CDH23):c.*515C>A	rs16929375
NM_022124.6(CDH23):c.*588del	rs148667421
NM_022124.6(CDH23):c.*68G>C	rs527311705
NM_022124.6(CDH23):c.*80G>A	rs75715348
NM_022124.6(CDH23):c.10026C>T (p.Asp3342=)	rs377118941
NM_022124.6(CDH23):c.9291G>T (p.Lys3097Asn)	rs368441850
NM_022124.6(CDH23):c.9319+11G>A	rs11000013
NM_022124.6(CDH23):c.9373T>C (p.Phe3125Leu)	rs45583140
NM_022124.6(CDH23):c.9501G>A (p.Thr3167=)	rs144906721
NM_022124.6(CDH23):c.9510+13C>T	rs183692794
NM_022124.6(CDH23):c.9510+19_9510+25del	rs149704197
NM_022124.6(CDH23):c.9629T>C (p.Ile3210Thr)	rs144688588
NM_022124.6(CDH23):c.9739-12G>A	rs200638595
NM_022124.6(CDH23):c.9758A>C (p.Asp3253Ala)	rs140463385
NM_022124.6(CDH23):c.9799C>T (p.Arg3267Cys)	rs201727938
NM_022124.6(CDH23):c.9860G>A (p.Gly3287Asp)	rs562590210
NM_022124.6(CDH23):c.9873G>A (p.Thr3291=)	rs2290021
NM_022124.6(CDH23):c.9903C>T (p.Pro3301=)	rs55717455
NM_022124.6(CDH23):c.9942G>A (p.Thr3314=)	rs376804660
NM_022124.6(CDH23):c.9978C>T (p.Asn3326=)	rs73277900
NM_022124.6(CDH23):c.9983G>A (p.Arg3328His)	rs148475933

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