No paralogue variants have been mapped to residue 491 for KCNH2.
KCNH2 | FIVDI-LINFRTTYVN-ANEEVVSHPGRIA>V<HYFKGW-FLIDMVAAIPFDLLIFGSGSEE- | 519 |
KCNH1 | FLVDI-VLNFHTTFVG-PAGEVISDPKLIR>M<NYLKTW-FVIDLLSCLPYDVINAFENVDEV | 318 |
KCNH3 | FILDI-VLNFRTTFVS-KSGQVVFAPKSIC>L<HYVTTW-FLLDVIAALPFDLLHAF-KVN-- | 326 |
KCNH4 | FILDI-ILNFRTTYVS-QSGQVISAPRSIG>L<HYLATW-FFIDLIAALPFDLLYIF-NIT-- | 328 |
KCNH5 | FLVDI-VLNFHTTFVG-PGGEVISDPKLIR>M<NYLKTW-FVIDLLSCLPYDIINAFENVDEG | 315 |
KCNH6 | FVVDI-VINFRTTYVN-TNDEVVSHPRRIA>V<HYFKGW-FLIDMVAAIPFDLLIFRTGSDE- | 367 |
KCNH7 | FIIDI-LINFRTTYVN-QNEEVVSDPAKIA>I<HYFKGW-FLIDMVAAIPFDLLIFGSGSDE- | 518 |
KCNH8 | FIIDI-ILNFRTTYVS-KSGQVIFEARSIC>I<HYVTTW-FIIDLIAALPFDLLYAF-NVT-- | 322 |
CNGA1 | YLIDM-FVRTRTGYLE--QGLLVKEELKLI>N<KYKSNLQFKLDVLSLIPTDLLYFKLGWNY- | 267 |
CNGA2 | YIADL-FIRLRTGFLE--QGLLVKDTKKLR>D<NYIHTLQFKLDVASIIPTDLIYFAVDIHS- | 242 |
CNGA3 | YVLDV-LVRARTGFLE--QGLMVSDTNRLW>Q<HYKTTTQFKLDVLSLVPTDLAYLKVGTNY- | 270 |
CNGA4 | YLLDM-VVRFHTGFLE--QGILVVDKGRIS>S<RYVRTWSFFLDLASLMPTDVVYVRLGPHT- | 136 |
CNGB1 | YFLDITVFQTRLQFVR--GGDIITDKKDMR>N<NYLKSRRFKMDLLSLLPLDFLYLKVGVN-- | 758 |
CNGB3 | YLYDMLFIQPRLQFVR--GGDIIVDSNELR>K<HYRTSTKFQLDVASIIPFDICYLFFGFN-- | 320 |
HCN1 | FLLDL-IMNFRTGTVNEDSSEIILDPKVIK>M<NYLKSW-FVVDFISSIPVDYIFLIVEK--G | 242 |
HCN2 | FLMDL-VLNFRTGIVIEDNTEIILDPEKIK>K<KYLRTW-FVVDFVSSIPVDYIFLIVEK--G | 311 |
HCN3 | FLLDL-VLNFRTGIVVEEGAEILLAPRAIR>T<RYLRTW-FLVDLISSIPVDYIFLVVELEPR | 195 |
HCN4 | FLIDL-VLNFRTGIVVEDNTEIILDPQRIK>M<KYLKSW-FMVDFISSIPVDYIFLIVET--R | 362 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.V491I | c.1471G>A | Putative Benign | rs374376640 | SIFT: tolerated Polyphen: benign |