Transcript #00015137

Transcript name proline-rich coiled-coil 2C
Gene name PRRC2C (proline-rich coiled-coil 2C)
Chromosome 1
Transcript - NCBI ID NM_015172.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_055987.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

351 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-32G>C r.(=) p.(=)
?/? c.77A>T r.(?) p.(Tyr26Phe)
?/? c.90A>G r.(=) p.(=)
?/? c.112+20A>G r.(=) p.(=)
?/? c.112+25T>C r.(=) p.(=)
?/? c.112+51A>T r.(=) p.(=)
?/? c.113-17T>C r.(=) p.(=)
?/? c.113-15G>T r.(=) p.(=)
?/? c.144C>T r.(=) p.(=)
?/? c.209A>G r.(?) p.(Asn70Ser)
?/? c.238G>T r.(?) p.(Asp80Tyr)
?/? c.255A>G r.(=) p.(=)
?/? c.284+15G>A r.(=) p.(=)
?/? c.285-36A>G r.(=) p.(=)
?/? c.285-12del r.(=) p.(=)
?/? c.290C>G r.(?) p.(Pro97Arg)
?/? c.304G>A r.(?) p.(Ala102Thr)
?/? c.327A>C r.(=) p.(=)
?/? c.328G>T r.(?) p.(Ala110Ser)
?/? c.335C>G r.(?) p.(Pro112Arg)
?/? c.343G>A r.(?) p.(Ala115Thr)
?/? c.360A>C r.(=) p.(=)
?/? c.364G>T r.(?) p.(Ala122Ser)
?/? c.394+21G>A r.(=) p.(=)
?/? c.394+33G>A r.(=) p.(=)
?/? c.394+47G>C r.(=) p.(=)
?/? c.394+47_394+51del r.(=) p.(=)
?/? c.395-15_395-14insA r.(=) p.(=)
?/? c.395-6C>A r.(=) p.(=)
?/? c.395-4A>G r.spl? p.?
?/? c.401A>G r.(?) p.(Gln134Arg)
?/? c.418C>G r.(?) p.(Gln140Glu)
?/? c.432C>T r.(=) p.(=)
?/? c.512G>A r.(?) p.(Arg171His)
?/? c.520A>G r.(?) p.(Asn174Asp)
?/? c.520+18T>C r.(=) p.(=)
?/? c.520+32del r.(=) p.(=)
?/? c.619A>G r.(?) p.(Thr207Ala)
?/? c.660G>A r.(=) p.(=)
?/? c.676C>T r.(?) p.(Pro226Ser)
?/? c.692A>G r.(?) p.(Asn231Ser)
?/? c.703G>A r.(?) p.(Ala235Thr)
?/? c.730A>G r.(?) p.(Met244Val)
?/? c.730_732del r.(?) p.(Met245del)
?/? c.732G>T r.(?) p.(Met244Ile)
?/? c.739C>G r.(?) p.(Pro247Ala)
?/? c.744+7A>G r.(=) p.(=)
?/? c.744+44G>C r.(=) p.(=)
?/? c.771A>G r.(=) p.(=)
?/? c.827+27G>A r.(=) p.(=)
?/? c.828-41C>T r.(=) p.(=)
?/? c.828-31T>C r.(=) p.(=)
?/? c.828-5A>G r.spl? p.?
?/? c.867T>C r.(=) p.(=)
?/? c.897A>G r.(=) p.(=)
?/? c.969G>A r.(=) p.(=)
?/? c.1025G>A r.(?) p.(Ser342Asn)
?/? c.1029C>G r.(?) p.(Asn343Lys)
?/? c.1049+51A>G r.(=) p.(=)
?/? c.1050-29T>C r.(=) p.(=)
?/? c.1054G>A r.(?) p.(Asp352Asn)
?/? c.1057C>A r.(?) p.(Gln353Lys)
?/? c.1080del r.(?) p.(Asn360Lysfs*26)
?/? c.1110T>C r.(=) p.(=)
?/? c.1133A>G r.(?) p.(Gln378Arg)
?/? c.1141G>C r.(?) p.(Ala381Pro)
?/? c.1169A>G r.(?) p.(Tyr390Cys)
?/? c.1194+13C>A r.(=) p.(=)
?/? c.1195-55A>G r.(=) p.(=)
?/? c.1195-46G>C r.(=) p.(=)
?/? c.1195-35A>G r.(=) p.(=)
?/? c.1195-2A>G r.spl? p.?
?/? c.1208C>T r.(?) p.(Ser403Phe)
?/? c.1216C>G r.(?) p.(Leu406Val)
?/? c.1231A>G r.(?) p.(Lys411Glu)
?/? c.1233G>A r.(=) p.(=)
?/? c.1248+16T>A r.(=) p.(=)
?/? c.1248+34del r.(=) p.(=)
?/? c.1248+39_1248+40del r.(=) p.(=)
?/? c.1248+71_1248+72insT r.(=) p.(=)
?/? c.1249-22A>C r.(=) p.(=)
?/? c.1249-14C>A r.(=) p.(=)
?/? c.1289G>A r.(?) p.(Gly430Asp)
?/? c.1302C>G r.(=) p.(=)
?/? c.1370C>G r.(?) p.(Ala457Gly)
?/? c.1500T>G r.(=) p.(=)
?/? c.1509A>G r.(=) p.(=)
?/? c.1519A>G r.(?) p.(Arg507Gly)
?/? c.1543C>T r.(?) p.(Arg515Cys)
?/? c.1544G>A r.(?) p.(Arg515His)
?/? c.1555C>T r.(?) p.(Leu519Phe)
?/? c.1571A>C r.(?) p.(Glu524Ala)
?/? c.1688_1690del r.(?) p.(Glu564del)
?/? c.1694_1696del r.(?) p.(Glu566del)
?/? c.1705C>T r.(?) p.(Arg569Trp)
?/? c.1809A>C r.(?) p.(Arg603Ser)
?/? c.1867+10T>C r.(=) p.(=)
?/? c.1867+12_1867+14del r.(=) p.(=)
?/? c.1867+18A>T r.(=) p.(=)
?/? c.1867+36T>C r.(=) p.(=)
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