No paralogue variants have been mapped to residue 928 for KCNH2.
KCNH2 | GEVSALGPGRAGAGPSSRGRPGG---P--W>G<ESPSSGPSS-------PESSEDEGP---GR | 948 |
KCNH1 | RQQKEARL-AAERGGRDLDDLDV---E--K>G<NVLTEHASA-------NHSLVKASV---VT | 789 |
KCNH3 | TDGEQG---P-TVSPAPADEPSS---P--L>L<SPGCTSSSSAAKLLSPRRTAPRPRL---GG | 781 |
KCNH4 | SGAEPGGGPRPR-RPLLLPNLSP---A--R>P<R--GSLVSLLGEELPPFSALVSSPS---LS | 779 |
KCNH5 | KQQKELRNQGSTQGDPERNQLQV---E--S>R<SLQNGASIT-------GTSVVTVSQ---IT | 759 |
KCNH6 | KGYSLLGPGSQNSMG------AG---P--C>A<PG-HPDAAP-------PLSISDASG---LW | 795 |
KCNH7 | --NSTNDPEDSADTIRHYQSSKR---H--F>E<EKKSRSSSF-------ISSIDDEQK---PL | 948 |
KCNH8 | EEEEEGEEEEAVSLSPICTRGSS---S--R>N<KKVGSNKAYLGLSLKQLASGT-VPF---HS | 765 |
CNGA1 | EYESMQQKLKQRLTKVEKFLKP-----LID>T<EFSSIEGPG---------AESGPID---S- | 689 |
CNGA2 | EYTGAQQKLKQRITVLETKMKQ-----NNE>D<DYLSDGMNS---------PELAAAD---E- | 663 |
CNGA3 | EYNATQMKMKQRLSQLESQVKG-----GG->D<KPLADGEVPG-------DATKTEDK---Q- | 693 |
CNGA4 | ELESSALKIAYRIERLEWQTREW---PMPE>D<LAEADDEGE---------PEEGTSK---DE | 562 |
CNGB1 | LAHLRARLKELAALEAAAKQQEL---V--E>Q<AKSSQDVKGE-------EGSAAPDQ----- | 1172 |
CNGB3 | -----ARLLKLKREQAAQKKENSEGGE--E>E<GKENEDKQKE-------NEDKQKEN----- | 730 |
HCN1 | QAIAPINYPQMTTLNSTSSTTTP---T--S>R<MRTQSPPVYT-------ATSLSHSNL-H-- | 679 |
HCN2 | QQAELGQRVGLFPPPPPPPQVTS---A--I>A<TLQQAAAMSF-------CPQVARPLVGP-- | 749 |
HCN3 | RGVRGRAPSTGAQLSGKPVLWEP---L--V>H<APLQAAAVTS-------NVAIALTHQRG-- | 629 |
HCN4 | HCAHRVQAAASATPTPTPVIWTP---L--I>Q<APLQAAAATT-------SVAIALTHHPRLP | 802 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.G928E | c.2783G>A | Unknown | SIFT: tolerated Polyphen: benign |