List of variants in gene CASR reported as uncertain significance by Martin Pollak Laboratory, Beth Israel Deaconess Medical Center

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.1192G>A (p.Asp398Asn)	rs201177696	0.00052
NM_000388.4(CASR):c.2777A>G (p.Gln926Arg)	rs200263975	0.00012
NM_000388.4(CASR):c.740C>T (p.Ser247Phe)	rs200382161	0.00010
NM_000388.4(CASR):c.1668G>A (p.Glu556=)	rs186279271	0.00003
NM_000388.4(CASR):c.1069A>T (p.Asn357Tyr)	rs387907392
NM_000388.4(CASR):c.1209T>C (p.Ser403=)	rs387907400
NM_000388.4(CASR):c.1395G>A (p.Arg465=)	rs387907391
NM_000388.4(CASR):c.1629C>T (p.Ser543=)	rs387907399
NM_000388.4(CASR):c.2597G>T (p.Arg866Leu)	rs387907401
NM_000388.4(CASR):c.2920A>T (p.Thr974Ser)	rs387907396
NM_000388.4(CASR):c.2944C>T (p.Pro982Ser)	rs387907395
NM_000388.4(CASR):c.3107T>C (p.Val1036Ala)	rs387907393
NM_000388.4(CASR):c.501T>C (p.Tyr167=)	rs387907394
NM_000388.4(CASR):c.920T>C (p.Met307Thr)	rs387907397
NM_000388.4(CASR):c.99C>T (p.Ile33=)	rs387907398

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