LRP1 inframe variants in ExAC


The table below lists the LRP1 inframe variants found in the ExAC population database. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.




No. Genomic coord. Variant (CDS) Variant (Protein) Variant Type ExAC frequencyPopulations*
1. 57597283 c.10930_10932delGAG p.Glu3645del inframe 0.00021529
2. 57599014 c.11317_11319delGAG p.Glu3774del inframe 0.00001670
3. 57598927 c.11230_11232delAAG p.Lys3745del inframe 0.00001657
4. 57598962 c.11265_11267delCTC p.Ser3758del inframe 0.00001656
5. 57605011 c.12969_12970insTCA p.Asp4323_Gly4324insSer inframe 0.00001651
6. 57605740 c.13289_13291dupTGC p.Leu4431dup inframe 0.00001648
7. 57605740 c.13289_13291delTGC p.Leu4433del inframe 0.00001648
8. 57605733 c.13282_13283insTGCTGT p.Leu4428_Leu4429insLeuLeu inframe 0.00000824
9. 57532348 c.174_175insGAGGCCCCTGAGATTTGTAAGTACCTTTTCTGGATT p.Asp58_Glu59insGluAlaProGluIleCysLysTyrLeuPheTrpI inframe 0.00000824

* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish. Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.

Genomic coordinates refer to the GRCh37 release of the human genome.