List of variants in gene PPP1R9B reported as not provided by Psychiatry Genetics Yale University

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_032595.5(PPP1R9B):c.1509C>T (p.Ser503=)	rs199601113	0.00070
NM_032595.5(PPP1R9B):c.1332C>T (p.Ala444=)	rs200300107	0.00049
NM_032595.5(PPP1R9B):c.1112C>T (p.Ala371Val)	rs367543188	0.00029
NM_032595.5(PPP1R9B):c.1590C>T (p.Thr530=)	rs201313568	0.00026
NM_032595.5(PPP1R9B):c.2238G>A (p.Ala746=)	rs367543183	0.00014
NM_032595.5(PPP1R9B):c.1137A>G (p.Val379=)	rs199865066	0.00011
NM_032595.5(PPP1R9B):c.336G>A (p.Lys112=)	rs367543204	0.00010
NM_032595.5(PPP1R9B):c.1916C>T (p.Pro639Leu)	rs367543185	0.00003
NM_032595.5(PPP1R9B):c.506G>A (p.Arg169Gln)	rs367543201	0.00002
NM_032595.5(PPP1R9B):c.1074G>C (p.Ala358=)	rs367543191	0.00001
NM_032595.5(PPP1R9B):c.1131G>A (p.Glu377=)	rs367543187	0.00001
NM_032595.5(PPP1R9B):c.1582G>A (p.Val528Ile)	rs367543186	0.00001
NM_032595.5(PPP1R9B):c.2199G>T (p.Leu733=)	rs367543184	0.00001
NM_032595.5(PPP1R9B):c.2358G>A (p.Ser786=)	rs367543182	0.00001
NM_032595.5(PPP1R9B):c.253C>T (p.Arg85Trp)	rs367543205	0.00001
NM_032595.5(PPP1R9B):c.1047A>G (p.Gln349=)	rs367543194
NM_032595.5(PPP1R9B):c.1059G>C (p.Glu353Asp)	rs367543193
NM_032595.5(PPP1R9B):c.1071G>A (p.Ala357=)	rs367543192
NM_032595.5(PPP1R9B):c.1077A>G (p.Val359=)	rs367543190
NM_032595.5(PPP1R9B):c.1092G>A (p.Arg364=)	rs367543189
NM_032595.5(PPP1R9B):c.198G>C (p.Thr66=)	rs367543206
NM_032595.5(PPP1R9B):c.513G>A (p.Leu171=)	rs367543200
NM_032595.5(PPP1R9B):c.579C>G (p.Thr193=)	rs367543199
NM_032595.5(PPP1R9B):c.631C>T (p.Leu211Phe)	rs367543198
NM_032595.5(PPP1R9B):c.729G>A (p.Leu243=)	rs367543197
NM_032595.5(PPP1R9B):c.777C>G (p.Pro259=)	rs367543196
NM_032595.5(PPP1R9B):c.815G>C (p.Cys272Ser)	rs367543195

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