All transcript variants in gene LPAR2

Information The variants shown are described using the NM_004720.5 transcript reference sequence.

45 entries on 1 page. Showing entries 1 - 45.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.1-15C>A r.(=) p.(=) g.19738108G>T Copied from the Exome Variant Server LPAR2_000045 1/12976 1/8574 0/4402
?/? c.1-4C>T r.spl? p.? g.19738097G>A Copied from the Exome Variant Server LPAR2_000044 91/12984 69/8584 22/4400
?/? c.41G>A r.(?) p.(Gly14Asp) g.19738053C>T Copied from the Exome Variant Server LPAR2_000043 2/13004 0/8600 2/4404
?/? c.102C>T r.(=) p.(=) g.19737992G>A Copied from the Exome Variant Server LPAR2_000042 43/13004 39/8600 4/4404
?/? c.228G>C r.(=) p.(=) g.19737866C>G Copied from the Exome Variant Server LPAR2_000041 1/13000 1/8596 0/4404
?/? c.240C>T r.(=) p.(=) g.19737854G>A Copied from the Exome Variant Server LPAR2_000040 2/13002 2/8600 0/4402
?/? c.259_261del r.(?) p.(Phe87del) g.19737833_19737835del Copied from the Exome Variant Server LPAR2_000039 24/12516 11/8254 13/4262
?/? c.261C>T r.(=) p.(=) g.19737833G>A Copied from the Exome Variant Server LPAR2_000038 2/13004 1/8600 1/4404
?/? c.264C>T r.(=) p.(=) g.19737830G>A Copied from the Exome Variant Server LPAR2_000037 1/13004 1/8600 0/4404
?/? c.289G>T r.(?) p.(Ala97Ser) g.19737805C>A Copied from the Exome Variant Server LPAR2_000036 1/13004 0/8600 1/4404
?/? c.295C>G r.(?) p.(Leu99Val) g.19737799G>C Copied from the Exome Variant Server LPAR2_000035 1/13004 1/8600 0/4404
?/? c.351G>A r.(=) p.(=) g.19737743C>T Copied from the Exome Variant Server LPAR2_000034 2/12978 2/8584 0/4394
?/? c.379G>A r.(?) p.(Val127Met) g.19737715C>T Copied from the Exome Variant Server LPAR2_000033 2/12968 0/8582 2/4386
?/? c.408G>A r.(=) p.(=) g.19737686C>T Copied from the Exome Variant Server LPAR2_000032 2305/12928 2066/8562 239/4366
?/? c.414G>A r.(=) p.(=) g.19737680C>T Copied from the Exome Variant Server LPAR2_000031 115/12920 0/8554 115/4366
?/? c.431G>A r.(?) p.(Arg144His) g.19737663C>T Copied from the Exome Variant Server LPAR2_000030 1/12908 1/8548 0/4360
?/? c.510C>T r.(=) p.(=) g.19737584G>A Copied from the Exome Variant Server LPAR2_000029 1/12988 1/8592 0/4396
?/? c.515_522del r.(?) p.(Leu172Profs*95) g.19737572_19737579del Copied from the Exome Variant Server LPAR2_000028 7/12504 5/8250 2/4254
?/? c.540C>T r.(=) p.(=) g.19737554G>A Copied from the Exome Variant Server LPAR2_000027 5/13004 5/8598 0/4406
?/? c.646C>A r.(=) p.(=) g.19737448G>T Copied from the Exome Variant Server LPAR2_000026 1/13006 0/8600 1/4406
?/? c.662G>A r.(?) p.(Arg221His) g.19737432C>T Copied from the Exome Variant Server LPAR2_000025 1/13006 1/8600 0/4406
?/? c.677T>G r.(?) p.(Val226Gly) g.19737417A>C Copied from the Exome Variant Server LPAR2_000024 1/13000 1/8594 0/4406
?/? c.707C>T r.(?) p.(Thr236Met) g.19737387G>A Copied from the Exome Variant Server LPAR2_000023 57/12998 52/8594 5/4404
?/? c.742+44del r.(=) p.(=) g.19737308del Copied from the Exome Variant Server LPAR2_000022 4/11970 3/7888 1/4082
?/? c.743-46G>A r.(=) p.(=) g.19735424C>T Copied from the Exome Variant Server LPAR2_000021 1/12970 1/8576 0/4394
?/? c.743-16C>T r.(=) p.(=) g.19735394G>A Copied from the Exome Variant Server LPAR2_000020 1/13004 0/8600 1/4404
?/? c.743-15G>A r.(=) p.(=) g.19735393C>T Copied from the Exome Variant Server LPAR2_000019 1/13004 0/8600 1/4404
?/? c.747G>A r.(=) p.(=) g.19735374C>T Copied from the Exome Variant Server LPAR2_000018 1/13006 1/8600 0/4406
?/? c.750C>T r.(=) p.(=) g.19735371G>A Copied from the Exome Variant Server LPAR2_000017 1/13006 0/8600 1/4406
?/? c.815A>C r.(?) p.(Asn272Thr) g.19735306T>G Copied from the Exome Variant Server LPAR2_000016 1/13006 0/8600 1/4406
?/? c.868G>A r.(?) p.(Val290Ile) g.19735253C>T Copied from the Exome Variant Server LPAR2_000015 1/13006 1/8600 0/4406
?/? c.873T>C r.(=) p.(=) g.19735248A>G Copied from the Exome Variant Server LPAR2_000014 89/13006 82/8600 7/4406
?/? c.892C>T r.(?) p.(Arg298*) g.19735229G>A Copied from the Exome Variant Server LPAR2_000013 1/13006 1/8600 0/4406
?/? c.908G>A r.(?) p.(Arg303His) g.19735213C>T Copied from the Exome Variant Server LPAR2_000012 2/13006 1/8600 1/4406
?/? c.910C>T r.(?) p.(Arg304Cys) g.19735211G>A Copied from the Exome Variant Server LPAR2_000011 1/13006 1/8600 0/4406
?/? c.920G>A r.(?) p.(Arg307His) g.19735201C>T Copied from the Exome Variant Server LPAR2_000010 3/13006 0/8600 3/4406
?/? c.936C>T r.(=) p.(=) g.19735185G>A Copied from the Exome Variant Server LPAR2_000009 5/13006 3/8600 2/4406
?/? c.937G>A r.(?) p.(Ala313Thr) g.19735184C>T Copied from the Exome Variant Server LPAR2_000008 1/13006 0/8600 1/4406
?/? c.943C>G r.(?) p.(Leu315Val) g.19735178G>C Copied from the Exome Variant Server LPAR2_000007 1/13006 1/8600 0/4406
?/? c.947G>A r.(?) p.(Arg316His) g.19735174C>T Copied from the Exome Variant Server LPAR2_000006 7/13006 4/8600 3/4406
?/? c.958C>T r.(?) p.(Arg320Cys) g.19735163G>A Copied from the Exome Variant Server LPAR2_000005 1/13006 1/8600 0/4406
?/? c.959G>A r.(?) p.(Arg320His) g.19735162C>T Copied from the Exome Variant Server LPAR2_000004 2/13006 1/8600 1/4406
?/? c.1032C>T r.(=) p.(=) g.19735089G>A Copied from the Exome Variant Server LPAR2_000003 1/13006 1/8600 0/4406
?/? c.*8G>A r.(=) p.(=) g.19735057C>T Copied from the Exome Variant Server LPAR2_000002 1/13006 0/8600 1/4406
?/? c.*22C>T r.(=) p.(=) g.19735043G>A Copied from the Exome Variant Server LPAR2_000001 129/13006 5/8600 124/4406
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