List of variants in gene CASR reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 34

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HGVS	dbSNP	gnomAD frequency
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.906C>T (p.Ser302=)	rs201067850	0.00063
NM_000388.4(CASR):c.915C>A (p.Ile305=)	rs200528343	0.00051
NM_000388.4(CASR):c.1733-9A>G	rs190731787	0.00044
NM_000388.4(CASR):c.1491C>T (p.Ser497=)	rs150337940	0.00035
NM_000388.4(CASR):c.27C>T (p.Val9=)	rs141880581	0.00016
NM_000388.4(CASR):c.492+18G>C	rs540628385	0.00016
NM_000388.4(CASR):c.1752G>A (p.Lys584=)	rs138638329	0.00014
NM_000388.4(CASR):c.546T>A (p.Ser182=)	rs200545177	0.00014
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.1188A>G (p.Thr396=)	rs200312817	0.00008
NM_000388.4(CASR):c.1044C>A (p.Ala348=)	rs753606065	0.00006
NM_000388.4(CASR):c.1827G>A (p.Thr609=)	rs200868156	0.00004
NM_000388.4(CASR):c.2769A>G (p.Pro923=)	rs199508670	0.00004
NM_000388.4(CASR):c.60C>T (p.Tyr20=)	rs201564143	0.00004
NM_000388.4(CASR):c.705C>A (p.Ile235=)	rs199887150	0.00004
NM_000388.4(CASR):c.2298C>T (p.His766=)	rs200723499	0.00002
NM_000388.4(CASR):c.3168G>T (p.Val1056=)	rs886057831	0.00002
NM_000388.4(CASR):c.1281T>C (p.Ile427=)	rs771741512	0.00001
NM_000388.4(CASR):c.1297G>C (p.Asp433His)	rs199511990	0.00001
NM_000388.4(CASR):c.2028G>A (p.Thr676=)	rs563112343	0.00001
NM_000388.4(CASR):c.2355C>T (p.Ala785=)	rs1472693542	0.00001
NM_000388.4(CASR):c.9_11del
NM_000388.4(CASR):c.1014T>C (p.His338=)	rs1553766831
NM_000388.4(CASR):c.1164G>A (p.Ser388=)	rs200898785
NM_000388.4(CASR):c.1378-21T>C
NM_000388.4(CASR):c.1572C>T (p.Asn524=)	rs776534485
NM_000388.4(CASR):c.1608+4G>T	rs878853974
NM_000388.4(CASR):c.2412C>T (p.Ala804=)	rs886038418
NM_000388.4(CASR):c.2901C>A (p.Ile967=)	rs199594582
NM_000388.4(CASR):c.309C>T (p.Thr103=)	rs373057548
NM_000388.4(CASR):c.78C>T (p.Ala26=)	rs77852524

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