List of variants in gene CA4 reported as likely benign for perceptual disorders

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000717.5(CA4):c.204A>G (p.Gly68=)	rs35468643	0.01491
NM_000717.5(CA4):c.375C>T (p.Gly125=)	rs148870395	0.00188
NM_000717.5(CA4):c.807T>C (p.Asn269=)	rs142961963	0.00057
NM_000717.5(CA4):c.761A>C (p.Gln254Pro)	rs150432787	0.00026
NM_000717.5(CA4):c.235C>A (p.Gln79Lys)	rs531909330	0.00012
NM_000717.5(CA4):c.435A>G (p.Lys145=)	rs201241903	0.00012
NM_000717.5(CA4):c.415A>T (p.Met139Leu)	rs185658468	0.00009
NM_000717.5(CA4):c.128G>T (p.Gly43Val)	rs563335203	0.00001
NM_000717.5(CA4):c.357C>T (p.Ser119=)	rs765898059	0.00001
NM_000717.5(CA4):c.483C>T (p.Asp161=)
NM_000717.5(CA4):c.788C>G (p.Thr263Arg)

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