List of variants in gene PPP1R15B reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_032833.5(PPP1R15B):c.1886C>G (p.Ser629Cys)	rs111725786	0.00447
NM_032833.5(PPP1R15B):c.430G>A (p.Glu144Lys)	rs4492688	0.00418
NM_032833.5(PPP1R15B):c.136G>A (p.Gly46Arg)	rs149785262	0.00204
NM_032833.5(PPP1R15B):c.76C>T (p.Pro26Ser)	rs12094135	0.00145
NM_032833.5(PPP1R15B):c.156C>T (p.Ser52=)	rs147611819	0.00087
NM_032833.5(PPP1R15B):c.255C>T (p.Ser85=)	rs143907441	0.00044
NM_032833.5(PPP1R15B):c.308A>G (p.Tyr103Cys)	rs137955986	0.00024
NM_032833.5(PPP1R15B):c.1516G>A (p.Glu506Lys)	rs150224664	0.00021
NM_032833.5(PPP1R15B):c.1308C>T (p.Asp436=)	rs377038976	0.00007
NM_032833.5(PPP1R15B):c.987C>T (p.His329=)	rs767849759	0.00003
NM_032833.5(PPP1R15B):c.1791C>T (p.Ala597=)
NM_032833.5(PPP1R15B):c.1973G>A (p.Arg658His)	rs759466766
NM_032833.5(PPP1R15B):c.555G>C (p.Leu185=)

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