Transcript #00007055

Transcript name G protein-coupled receptor 158
Gene name GPR158 (G protein-coupled receptor 158)
Chromosome 10
Transcript - NCBI ID NM_020752.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_065803.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

174 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-40del r.(=) p.(=)
?/? c.-40dup r.(=) p.(=)
?/? c.-35C>G r.(=) p.(=)
?/? c.-33C>T r.(=) p.(=)
?/? c.14C>T r.(?) p.(Ala5Val)
?/? c.106C>G r.(?) p.(Arg36Gly)
?/? c.116C>T r.(?) p.(Thr39Ile)
?/? c.165G>A r.(=) p.(=)
?/? c.173C>T r.(?) p.(Ser58Leu)
?/? c.178C>A r.(?) p.(Pro60Thr)
?/? c.187C>T r.(?) p.(Arg63Cys)
?/? c.195C>A r.(=) p.(=)
?/? c.247G>A r.(?) p.(Ala83Thr)
?/? c.302G>T r.(?) p.(Gly101Val)
?/? c.326C>T r.(?) p.(Pro109Leu)
?/? c.402C>T r.(=) p.(=)
?/? c.502G>A r.(?) p.(Glu168Lys)
?/? c.522G>A r.(=) p.(=)
?/? c.546G>A r.(=) p.(=)
?/? c.604C>G r.(?) p.(Leu202Val)
?/? c.660C>G r.(=) p.(=)
?/? c.712G>A r.(?) p.(Gly238Ser)
?/? c.719A>G r.(?) p.(Asn240Ser)
?/? c.771C>T r.(=) p.(=)
?/? c.812A>G r.(?) p.(Glu271Gly)
?/? c.860C>T r.(?) p.(Ser287Phe)
?/? c.871G>C r.(?) p.(Gly291Arg)
?/? c.902+21del r.(=) p.(=)
?/? c.902+30G>A r.(=) p.(=)
?/? c.903-48C>T r.(=) p.(=)
?/? c.903G>A r.(=) p.(=)
?/? c.942C>T r.(=) p.(=)
?/? c.962A>G r.(?) p.(Asp321Gly)
?/? c.1008+6A>G r.(=) p.(=)
?/? c.1008+37G>A r.(=) p.(=)
?/? c.1008+49T>G r.(=) p.(=)
?/? c.1009-19T>C r.(=) p.(=)
?/? c.1026C>A r.(=) p.(=)
?/? c.1027C>G r.(?) p.(Leu343Val)
?/? c.1036G>A r.(?) p.(Val346Ile)
?/? c.1040T>C r.(?) p.(Leu347Pro)
?/? c.1079A>G r.(?) p.(His360Arg)
?/? c.1081C>A r.(?) p.(Pro361Thr)
?/? c.1108C>T r.(?) p.(Arg370Trp)
?/? c.1111+20A>G r.(=) p.(=)
?/? c.1111+22_1111+23insTA r.(=) p.(=)
?/? c.1112-24_1112-23del r.(=) p.(=)
?/? c.1121C>T r.(?) p.(Pro374Leu)
?/? c.1137A>C r.(=) p.(=)
?/? c.1200C>T r.(=) p.(=)
?/? c.1250G>A r.(?) p.(Arg417Gln)
?/? c.1274C>G r.(?) p.(Ala425Gly)
?/? c.1288C>T r.(?) p.(Leu430Phe)
?/? c.1335+36C>G r.(=) p.(=)
?/? c.1336-10_1336-9insT r.(=) p.(=)
?/? c.1342C>T r.(?) p.(Arg448Trp)
?/? c.1362G>C r.(=) p.(=)
?/? c.1375C>T r.(?) p.(Leu459Phe)
?/? c.1404+33A>G r.(=) p.(=)
?/? c.1404+49A>C r.(=) p.(=)
?/? c.1405-42A>G r.(=) p.(=)
?/? c.1405-9A>G r.(=) p.(=)
?/? c.1424A>G r.(?) p.(Glu475Gly)
?/? c.1439G>A r.(?) p.(Arg480His)
?/? c.1463G>A r.(?) p.(Arg488His)
?/? c.1465C>G r.(?) p.(Leu489Val)
?/? c.1488C>T r.(=) p.(=)
?/? c.1514+9_1514+10insT r.(=) p.(=)
?/? c.1515-26T>C r.(=) p.(=)
?/? c.1515-9C>A r.(=) p.(=)
?/? c.1515-9del r.(=) p.(=)
?/? c.1515-3T>C r.spl? p.?
?/? c.1528_1531del r.(?) p.(Leu511Hisfs*10)
?/? c.1542G>A r.(=) p.(=)
?/? c.1567G>A r.(?) p.(Gly523Ser)
?/? c.1569C>T r.(=) p.(=)
?/? c.1570G>A r.(?) p.(Gly524Arg)
?/? c.1573C>T r.(?) p.(Arg525Trp)
?/? c.1584G>A r.(=) p.(=)
?/? c.1683G>A r.(=) p.(=)
?/? c.1684G>A r.(?) p.(Gly562Arg)
?/? c.1695C>T r.(=) p.(=)
?/? c.1696G>A r.(?) p.(Asp566Asn)
?/? c.1704C>T r.(=) p.(=)
?/? c.1753+25_1753+35del r.(=) p.(=)
?/? c.1797A>G r.(=) p.(=)
?/? c.1801C>T r.(?) p.(Arg601Trp)
?/? c.1842_1843insGGTG r.(?) p.(Val615Glyfs*7)
?/? c.1893-17A>G r.(=) p.(=)
?/? c.1995A>G r.(=) p.(=)
?/? c.1998+19_1998+20del r.(=) p.(=)
?/? c.1998+20del r.(=) p.(=)
?/? c.1998+20dup r.(=) p.(=)
?/? c.1998+39del r.(=) p.(=)
?/? c.1998+39T>C r.(=) p.(=)
?/? c.1998+50C>T r.(=) p.(=)
?/? c.1999-46C>T r.(=) p.(=)
?/? c.1999-39G>A r.(=) p.(=)
?/? c.2024G>A r.(?) p.(Arg675Gln)
?/? c.2102A>G r.(?) p.(Asn701Ser)
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