List of variants in gene CASR reported as likely benign for bone disorder

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_000388.4(CASR):c.2610G>A (p.Glu870=)	rs143738711	0.01002
NM_000388.4(CASR):c.748G>A (p.Glu250Lys)	rs62269092	0.00163
NM_000388.4(CASR):c.1631G>A (p.Arg544Gln)	rs115230894	0.00086
NM_000388.4(CASR):c.1285C>T (p.His429Tyr)	rs142818334	0.00073
NM_000388.4(CASR):c.915C>A (p.Ile305=)	rs200528343	0.00051
NM_000388.4(CASR):c.2824G>A (p.Glu942Lys)	rs76327999	0.00034
NM_000388.4(CASR):c.*87C>T	rs202045621	0.00020
NM_000388.4(CASR):c.27C>T (p.Val9=)	rs141880581	0.00016
NM_000388.4(CASR):c.573G>A (p.Glu191=)	rs141631116	0.00016
NM_000388.4(CASR):c.1788C>T (p.Thr596=)	rs142778221	0.00009
NM_000388.4(CASR):c.2844G>A (p.Leu948=)	rs140586950	0.00009
NM_000388.4(CASR):c.825T>C (p.Asp275=)	rs199836910	0.00007
NM_000388.4(CASR):c.1554A>G (p.Gly518=)	rs138099808	0.00006
NM_000388.4(CASR):c.762T>C (p.His254=)	rs76438850	0.00006
NM_000388.4(CASR):c.1377+17T>C	rs200650843	0.00002
NM_000388.4(CASR):c.675A>G (p.Lys225=)	rs202226622	0.00002
NM_000388.4(CASR):c.909C>G (p.Ser303=)	rs375005541	0.00002
NM_000388.4(CASR):c.1452C>T (p.Asp484=)	rs776775141	0.00001
NM_000388.4(CASR):c.1887T>C (p.Phe629=)	rs750220557	0.00001
NM_000388.4(CASR):c.2046G>A (p.Pro682=)	rs760450976	0.00001
NM_000388.4(CASR):c.2139C>T (p.Ser713=)	rs200384325	0.00001
NM_000388.4(CASR):c.2767C>G (p.Pro923Ala)	rs201517907	0.00001
NM_000388.4(CASR):c.2994G>A (p.Leu998=)	rs200260696	0.00001
NM_000388.4(CASR):c.3018G>A (p.Thr1006=)	rs748637478	0.00001
NM_000388.4(CASR):c.537A>G (p.Gln179=)	rs200129212	0.00001
NM_000388.4(CASR):c.738C>T (p.Tyr246=)	rs895337411	0.00001
NM_000388.4(CASR):c.813C>A (p.Ser271=)	rs759939185	0.00001
NM_000388.4(CASR):c.-378del	rs537119483
NM_000388.4(CASR):c.1008G>C (p.Lys336Asn)	rs548403340
NM_000388.4(CASR):c.1116C>T (p.Thr372=)	rs539867627
NM_000388.4(CASR):c.1164G>A (p.Ser388=)	rs200898785
NM_000388.4(CASR):c.2439C>T (p.Ile813=)	rs1228810304
NM_000388.4(CASR):c.3234A>G (p.Ser1078=)	rs556263764
NM_000388.4(CASR):c.493-12G>T	rs199514129
NM_000388.4(CASR):c.54T>G (p.Ser18=)	rs558522564
NM_000388.4(CASR):c.876C>T (p.Ile292=)	rs772232871

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