CPVL

carboxypeptidase vitellogenic like

Summary

The protein encoded by this gene is a carboxypeptidase and bears strong sequence similarity to serine carboxypeptidases. Carboxypeptidases are a large class of proteases that act to cleave a single amino acid from the carboxy termini of proteins or peptides. The exact function of this protein, however, has not been determined. [provided by RefSeq, Jan 2017]

Known Variants43 total

rsidPosition (GRCh37)AllelesClassClinVar
rs2016132807:29,035,396C/Auncertain significance
rs1477714777:29,035,428C/Tlikely benign
rs22525217:29,041,190T/A
rs14595036207:29,070,254T/Guncertain significance
rs9494710357:29,070,267T/Cuncertain significance
rs5610086007:29,070,296T/Cuncertain significance
rs7767193977:29,070,342C/Tuncertain significance
rs25357473717:29,103,703A/Cuncertain significance
rs25357477177:29,103,727T/Cuncertain significance
rs17829133337:29,103,751C/Guncertain significance
rs12005218467:29,103,847G/Auncertain significance
rs1395061367:29,105,665T/Guncertain significance
rs1913493647:29,111,948G/Auncertain significance
rs5712011807:29,116,438T/C
rs1179385967:29,125,328T/Cdownstream gene variant
rs3768169387:29,126,102C/Guncertain significance
rs1477010807:29,126,849A/Gdownstream gene variant
rs7756538287:29,132,269T/Guncertain significance
rs7515437327:29,132,282C/Tuncertain significance
rs3745103047:29,134,718C/Tuncertain significance
rs3765394167:29,134,755C/Tuncertain significance
rs7766043927:29,135,723C/Guncertain significance
rs115429827:29,135,787G/Auncertain significance
rs15842498417:29,135,820T/Auncertain significance
rs5303855247:29,139,759A/G
rs796792297:29,142,045G/Aintron variant
rs1458771697:29,146,764C/Aintron variant
rs3683196317:29,152,382C/Tuncertain significance
rs7558355567:29,152,411A/Guncertain significance
rs1867086457:29,154,200C/Tregulatory region variant
rs1472232857:29,156,341G/Cregulatory region variant
rs10523345347:29,160,532A/Guncertain significance
rs15627793457:29,160,593T/Cuncertain significance
rs25360944737:29,160,622G/Auncertain significance
rs11860305897:29,160,643A/Guncertain significance
rs17893191077:29,160,659T/Guncertain significance
rs1472040837:29,160,664A/Glikely benign
rs7648984997:29,160,670C/Tuncertain significance
rs1473922987:29,163,140C/Tupstream gene variant
rs132280177:29,163,329T/G
rs1896710087:29,164,953A/Cupstream gene variant
rs1510827717:29,166,225C/Tupstream gene variant
rs5469755647:29,176,733G/A

Gene information from NCBI Gene. Variant classifications from ClinVar.