No paralogue variants have been mapped to residue 13 for KCNH2.
KCNH2 | ----------------RR----G-HVAPQN>T<FLDTI---IR----KFEGQSRK-------- | 28 |
KCNH1 | ----------------RR----G-LVAPQN>T<FLENI---VR----RS--NDTN-------- | 29 |
KCNH3 | ----------------MR----G-LLAPQN>T<FLDTI---AT----RFDGTHSN-------- | 28 |
KCNH4 | ----------------MK----G-LLAPQN>T<FLDTI---AT----RFDGTHSN-------- | 28 |
KCNH5 | ----------------KR----G-LVAPQN>T<FLENI---VR----RS--SESS-------- | 27 |
KCNH6 | ----------------RR----G-HVAPQN>T<YLDTI---IR----KFEGQSRK-------- | 28 |
KCNH7 | ----------------RR----G-HVAPQN>T<FLGTI---IR----KFEGQNKK-------- | 28 |
KCNH8 | ----------------MK----G-LLAPQN>T<FLDTI---AT----RFDGTHSN-------- | 28 |
CNGA1 | ----------------SMK---NNIINTQQ>S<FVTMPNVIVP----DIEKE----------- | 30 |
CNGA2 | ----------------K--------TNGVK>-<-------SSP----AN-------------- | 14 |
CNGA3 | -------------------------INTQY>-<-------SHP----SRTH------------ | 15 |
CNGA4 | ------------------------------>-<------------------------------ | |
CNGB1 | ESESMPPEESFKEEEVAV-----ADPSPQE>T<KEAAL---TSTISLRAQGAEISEMNSPSRR | 101 |
CNGB3 | ------------------------------>-<------------------------------ | |
HCN1 | ----------------G------------->-<---------------GKPNS---------- | 9 |
HCN2 | ------------------------------>-<--RG-----G----GGRPGE---------- | 12 |
HCN3 | ----------------E------------->-<---------------QRPAA---------- | 9 |
HCN4 | ----------------LPPSMRKRLYSLPQ>Q<VGAK-----A----WIMDEE---------- | 29 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.T13N | c.38C>A | Inherited Arrhythmia | LQTS | SIFT: Polyphen: |