List of variants in gene PC reported as likely benign for not specified

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_001040716.2(PC):c.2223+19C>T	rs45457699	0.00153
NM_001040716.2(PC):c.1604-17G>A	rs79317761	0.00103
NM_001040716.2(PC):c.486G>A (p.Ala162=)	rs142416378	0.00041
NM_001040716.2(PC):c.*15G>A	rs45501894	0.00027
NM_001040716.2(PC):c.89G>A (p.Arg30Gln)	rs199616332	0.00019
NM_001040716.2(PC):c.571A>G (p.Ile191Val)	rs141543771	0.00014
NM_001040716.2(PC):c.2304G>C (p.Leu768=)	rs61731787	0.00011
NM_001040716.2(PC):c.50G>A (p.Arg17His)	rs375282341	0.00007
NM_001040716.2(PC):c.1767G>T (p.Lys589Asn)	rs143725101	0.00004
NM_001040716.2(PC):c.904-16G>A	rs189690730	0.00004
NM_001040716.2(PC):c.1519G>A (p.Val507Ile)	rs555210692	0.00003
NM_001040716.2(PC):c.3336C>T (p.Ile1112=)	rs776196411	0.00003
NM_001040716.2(PC):c.3033T>C (p.Ala1011=)	rs139740019	0.00002
NM_001040716.2(PC):c.1173C>T (p.Thr391=)	rs202135326	0.00001
NM_001040716.2(PC):c.14G>A (p.Arg5Gln)	rs753072659	0.00001
NM_001040716.2(PC):c.159C>T (p.Phe53=)	rs749641310	0.00001
NM_001040716.2(PC):c.2195G>A (p.Arg732Gln)	rs773872994	0.00001
NM_001040716.2(PC):c.2224-18C>A	rs768718604	0.00001
NM_001040716.2(PC):c.2657A>G (p.Lys886Arg)	rs796052027	0.00001
NM_001040716.2(PC):c.2706C>T (p.Gly902=)	rs73489729	0.00001
NM_001040716.2(PC):c.2880C>T (p.Pro960=)	rs549991937	0.00001
NM_001040716.2(PC):c.3288+20C>T	rs750712278	0.00001
NM_001040716.2(PC):c.927C>T (p.Thr309=)	rs373717650	0.00001
NM_001040716.2(PC):c.-228+9C>T	rs1555053361
NM_001040716.2(PC):c.1-37A>C	rs781186745
NM_001040716.2(PC):c.1023-14C>A	rs111858832
NM_001040716.2(PC):c.1140C>A (p.Thr380=)	rs369657359
NM_001040716.2(PC):c.1513+9C>A	rs45580638
NM_001040716.2(PC):c.1603+4G>T	rs923731755
NM_001040716.2(PC):c.2118C>T (p.Tyr706=)	rs771659705
NM_001040716.2(PC):c.3289-10G>C	rs529411023
NM_001040716.2(PC):c.634-4G>A	rs368096991
NM_001040716.2(PC):c.840C>T (p.Ala280=)	rs376393322
NM_001040716.2(PC):c.96G>A (p.Leu32=)	rs1057520946

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