Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73322434_73322472dup | CA619410571 | HCN4 | c.*17_*55dup (n.*17_*55dup) | gnomAD v2 gnomAD v4 |
15 | g.73322444G>A | CA2187185949 | HCN4 | c.*37C>T (n.*37C>T) | dbSNP gnomAD v4 |
15 | g.73322444G= | CA2187185951 | HCN4 | c.*37C= (n.*37C=) | |
15 | g.73322444G>T | CA2575783810 | HCN4 | c.*37C>A (n.*37C>A) | gnomAD v4 |
15 | g.73322445A>G | CA2629370486 | HCN4 | c.*36T>C (n.*36T>C) | gnomAD v4 |
15 | g.73322445A>T | CA2731232600 | HCN4 | c.*36T>A (n.*36T>A) | dbSNP |
15 | g.73322446G>A | CA272662922 | HCN4 | c.*35C>T (n.*35C>T) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322446G= | CA2187185953 | HCN4 | c.*35C= (n.*35C=) | |
15 | g.73322446G>T | CA2575783811 | HCN4 | c.*35C>A (n.*35C>A) | gnomAD v4 |
15 | g.73322447A>G | CA2629370487 | HCN4 | c.*34T>C (n.*34T>C) | gnomAD v4 |
15 | g.73322448A>G | CA2629370488 | HCN4 | c.*33T>C (n.*33T>C) | gnomAD v4 |
15 | g.73322448_73322451delinsAAAG | CA2187185955 | HCN4 | c.*30_*33delinsCTTT (n.*30_*33delinsCTTT) | |
15 | g.73322454_73322456del | CA491477743 | HCN4 | c.*30_*32del (n.*30_*32del) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322450A>G | CA2629370489 | HCN4 | c.*31T>C (n.*31T>C) | gnomAD v4 |
15 | g.73322451G>T | CA2575783812 | HCN4 | c.*30C>A (n.*30C>A) | gnomAD v4 |
15 | g.73322451_73322455delinsGAAGA | CA2187185960 | HCN4 | c.*26_*30delinsTCTTC (n.*26_*30delinsTCTTC) | |
15 | g.73322452A= | CA2187185962 | HCN4 | c.*29T= (n.*29T=) | |
15 | g.73322452A>G | CA2187185963 | HCN4 | c.*29T>C (n.*29T>C) | dbSNP |
15 | g.73322452A>T | CA2629370490 | HCN4 | c.*29T>A (n.*29T>A) | gnomAD v4 |
15 | g.73322457_73322460del | CA971394125 | HCN4 | c.*26_*29del (n.*26_*29del) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322453A>C | CA2804726806 | HCN4 | c.*28T>G (n.*28T>G) | |
15 | g.73322453A>G | CA2629370491 | HCN4 | c.*28T>C (n.*28T>C) | gnomAD v4 |
15 | g.73322453A>T | CA2629370492 | HCN4 | c.*28T>A (n.*28T>A) | gnomAD v4 |
15 | g.73322454G>C | CA2510755604 | HCN4 | c.*27C>G (n.*27C>G) | |
15 | g.73322454G= | CA2187185966 | HCN4 | c.*27C= (n.*27C=) | |
15 | g.73322454G>T | CA715542315 | HCN4 | c.*27C>A (n.*27C>A) | dbSNP gnomAD v4 |
15 | g.73322457dup | CA715542317 | HCN4 | c.*26dup (n.*26dup) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322457del | CA2629370493 | HCN4 | c.*26del (n.*26del) | gnomAD v4 |
15 | g.73322455_73322458delinsAAAG | CA2187185968 | HCN4 | c.*23_*26delinsCTTT (n.*23_*26delinsCTTT) | |
15 | g.73322456A>G | CA2629370494 | HCN4 | c.*25T>C (n.*25T>C) | gnomAD v4 |
15 | g.73322460_73322462del | CA2187185969 | HCN4 | c.*23_*25del (n.*23_*25del) | dbSNP gnomAD v4 |
15 | g.73322458G>A | CA2629370495 | HCN4 | c.*23C>T (n.*23C>T) | gnomAD v4 |
15 | g.73322458G>T | CA2629370496 | HCN4 | c.*23C>A (n.*23C>A) | gnomAD v4 |
15 | g.73322459A>C | CA2518978101 | HCN4 | c.*22T>G (n.*22T>G) | |
15 | g.73322460A>G | CA2629370497 | HCN4 | c.*21T>C (n.*21T>C) | gnomAD v4 |
15 | g.73322461G= | CA2187185971 | HCN4 | c.*20C= (n.*20C=) | |
15 | g.73322461G>T | CA2629370498 | HCN4 | c.*20C>A (n.*20C>A) | gnomAD v4 |
15 | g.73322462A>G | CA2629370499 | HCN4 | c.*19T>C (n.*19T>C) | gnomAD v4 |
15 | g.73322462_73322463insAAGAGAAAAGAGAAAAGAAAAGAA | CA619410572 | HCN4 | c.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT (n.*19_*20insTCTTTTCTTTTCTCTTTTCTCTTT) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322463G>A | CA619410573 | HCN4 | c.*18C>T (n.*18C>T) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322463G>C | CA2187185976 | HCN4 | c.*18C>G (n.*18C>G) | dbSNP gnomAD v4 |
15 | g.73322463G= | CA2187185974 | HCN4 | c.*18C= (n.*18C=) | |
15 | g.73322463G>T | CA2629370500 | HCN4 | c.*18C>A (n.*18C>A) | gnomAD v4 |
15 | g.73322464G>A | CA2629370502 | HCN4 | c.*17C>T (n.*17C>T) | gnomAD v4 |
15 | g.73322464G>T | CA2629370503 | HCN4 | c.*17C>A (n.*17C>A) | gnomAD v4 |
15 | g.73322470_73322473del | CA2629370501 | HCN4 | c.*14_*17del (n.*14_*17del) | gnomAD v4 |
15 | g.73322465G>T | CA2629370504 | HCN4 | c.*16C>A (n.*16C>A) | gnomAD v4 |
15 | g.73322467dup | CA2629370505 | HCN4 | c.*15dup (n.*15dup) | gnomAD v4 |
15 | g.73322467A= | CA2187185979 | HCN4 | c.*14T= (n.*14T=) | |
15 | g.73322467A>C | CA2187185980 | HCN4 | c.*14T>G (n.*14T>G) | dbSNP gnomAD v4 |
15 | g.73322467A>G | CA2543931915 | HCN4 | c.*14T>C (n.*14T>C) | gnomAD v4 |
15 | g.73322468G= | CA2187185982 | HCN4 | c.*13C= (n.*13C=) | |
15 | g.73322468G>T | CA619410574 | HCN4 | c.*13C>A (n.*13C>A) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322469G>A | CA7648787 | HCN4 | c.*12C>T (n.*12C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322469G= | CA2187185985 | HCN4 | c.*12C= (n.*12C=) | |
15 | g.73322469G>T | CA2629370506 | HCN4 | c.*12C>A (n.*12C>A) | gnomAD v4 |
15 | g.73322470A>C | CA2527337957 | HCN4 | c.*11T>G (n.*11T>G) | gnomAD v4 |
15 | g.73322470A>G | CA2629370507 | HCN4 | c.*11T>C (n.*11T>C) | gnomAD v4 |
15 | g.73322470A>T | CA2629370508 | HCN4 | c.*11T>A (n.*11T>A) | gnomAD v4 |
15 | g.73322471del | CA2629370509 | HCN4 | c.*11del (n.*11del) | gnomAD v4 |
15 | g.73322471A>C | CA971394130 | HCN4 | c.*10T>G (n.*10T>G) | gnomAD v3 gnomAD v4 |
15 | g.73322471A>G | CA2560564610 | HCN4 | c.*10T>C (n.*10T>C) | gnomAD v4 |
15 | g.73322471_73322472delinsAG | CA2187185987 | HCN4 | c.*9_*10delinsCT (n.*9_*10delinsCT) | |
15 | g.73322472G>A | CA619410576 | HCN4 | c.*9C>T (n.*9C>T) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322472G>C | CA2575783813 | HCN4 | c.*9C>G (n.*9C>G) | gnomAD v4 |
15 | g.73322472G= | CA2187185992 | HCN4 | c.*9C= (n.*9C=) | |
15 | g.73322472G>T | CA2629370510 | HCN4 | c.*9C>A (n.*9C>A) | gnomAD v4 |
15 | g.73322474del | CA619410575 | HCN4 | c.*9del (n.*9del) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322473G>A | CA7648788 | HCN4 | c.*8C>T (n.*8C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322473G>C | CA2575783814 | HCN4 | c.*8C>G (n.*8C>G) | gnomAD v4 |
15 | g.73322473G= | CA2187185997 | HCN4 | c.*8C= (n.*8C=) | |
15 | g.73322473G>T | CA619410577 | HCN4 | c.*8C>A (n.*8C>A) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322474G>A | CA2629370511 | HCN4 | c.*7C>T (n.*7C>T) | gnomAD v4 |
15 | g.73322474G>C | CA2575783815 | HCN4 | c.*7C>G (n.*7C>G) | gnomAD v4 |
15 | g.73322474G>T | CA2629370512 | HCN4 | c.*7C>A (n.*7C>A) | gnomAD v4 |
15 | g.73322475C>A | CA2629370513 | HCN4 | c.*6G>T (n.*6G>T) | gnomAD v4 |
15 | g.73322475C>T | CA2629370514 | HCN4 | c.*6G>A (n.*6G>A) | gnomAD v4 |
15 | g.73322476C>A | CA2629370515 | HCN4 | c.*5G>T (n.*5G>T) | gnomAD v4 |
15 | g.73322476C= | CA2187186000 | HCN4 | c.*5G= (n.*5G=) | |
15 | g.73322476C>T | CA2187186002 | HCN4 | c.*5G>A (n.*5G>A) | dbSNP |
15 | g.73322476_73322477insG | CA2540210855 | HCN4 | c.*4_*5insC (n.*4_*5insC) | |
15 | g.73322477C>A | CA971394140 | HCN4 | c.*4G>T (n.*4G>T) | gnomAD v3 gnomAD v4 |
15 | g.73322477C>T | CA2629370516 | HCN4 | c.*4G>A (n.*4G>A) | gnomAD v4 |
15 | g.73322478A>C | CA2629370517 | HCN4 | c.*3T>G (n.*3T>G) | gnomAD v4 |
15 | g.73322478A>G | CA2629370518 | HCN4 | c.*3T>C (n.*3T>C) | gnomAD v4 |
15 | g.73322479G>A | CA2629370519 | HCN4 | c.*2C>T (n.*2C>T) | gnomAD v4 |
15 | g.73322479G>C | CA2499223088 | HCN4 | c.*2C>G (n.*2C>G) | ClinVar dbSNP gnomAD v4 |
15 | g.73322479G>T | CA2629370520 | HCN4 | c.*2C>A (n.*2C>A) | gnomAD v4 |
15 | g.73322480C>A | CA2629370521 | HCN4 | c.*1G>T (n.*1G>T) | gnomAD v4 |
15 | g.73322480C>T | CA2804726808 | HCN4 | c.*1G>A (n.*1G>A) | |
15 | g.73322480_73322482del | CA2804726807 | HCN4 | c.3611_*1del (n.[c.3611_*1del;Ter1204SerextTer21]) c.2393_*1del (n.[c.2393_*1del;Ter798SerextTer21]) | |
15 | g.73322481T>A | CA393084579 | HCN4 | c.3612A>T (p.Ter1204Cys) c.2394A>T (p.Ter798Cys) | gnomAD v4 |
15 | g.73322481T>C | CA393084582 | HCN4 | c.3612A>G (p.Ter1204Trp) c.2394A>G (p.Ter798Trp) | gnomAD v4 |
15 | g.73322481T>G | CA393084586 | HCN4 | c.3612A>C (p.Ter1204Cys) c.2394A>C (p.Ter798Cys) | gnomAD v4 |
15 | g.73322482C>A | CA393084588 | HCN4 | c.3611G>T (p.Ter1204Leu) c.2393G>T (p.Ter798Leu) | gnomAD v4 |
15 | g.73322482C>G | CA393084590 | HCN4 | c.3611G>C (p.Ter1204Ser) c.2393G>C (p.Ter798Ser) | |
15 | g.73322482C>T | CA491477744 | HCN4 | c.3611G>A (p.Ter1204=) c.2393G>A (p.Ter798=) | gnomAD v4 |
15 | g.73322483A>C | CA393084592 | HCN4 | c.3610T>G (p.Ter1204Gly) c.2392T>G (p.Ter798Gly) | |
15 | g.73322483A>G | CA393084593 | HCN4 | c.3610T>C (p.Ter1204Arg) c.2392T>C (p.Ter798Arg) | gnomAD v4 |
15 | g.73322483A>T | CA393084595 | HCN4 | c.3610T>A (p.Ter1204Arg) c.2392T>A (p.Ter798Arg) | |
15 | g.73322484T>A | CA491477745 | HCN4 | c.3609A>T (p.Leu1203=) c.2391A>T (p.Leu797=) | |
15 | g.73322484T>C | CA7648789 | HCN4 | c.3609A>G (p.Leu1203=) c.2391A>G (p.Leu797=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322484T>G | CA491477746 | HCN4 | c.3609A>C (p.Leu1203=) c.2391A>C (p.Leu797=) | |
15 | g.73322484T= | CA2187186007 | HCN4 | c.3609A= (p.Leu1203=) c.2391A= (p.Leu797=) | |
15 | g.73322485A= | CA2187186016 | HCN4 | c.3608T= (p.Leu1203=) c.2390T= (p.Leu797=) | |
15 | g.73322485A>C | CA393084599 | HCN4 | c.3608T>G (p.Leu1203Arg) c.2390T>G (p.Leu797Arg) | |
15 | g.73322485A>G | CA393084600 | HCN4 | c.3608T>C (p.Leu1203Pro) c.2390T>C (p.Leu797Pro) | ClinVar dbSNP gnomAD v4 |
15 | g.73322485A>T | CA393084603 | HCN4 | c.3608T>A (p.Leu1203Gln) c.2390T>A (p.Leu797Gln) | |
15 | g.73322486G>A | CA491477747 | HCN4 | c.3607C>T (p.Leu1203=) c.2389C>T (p.Leu797=) | dbSNP gnomAD v4 |
15 | g.73322486G>C | CA393084605 | HCN4 | c.3607C>G (p.Leu1203Val) c.2389C>G (p.Leu797Val) | |
15 | g.73322486G>T | CA393084606 | HCN4 | c.3607C>A (p.Leu1203Ile) c.2389C>A (p.Leu797Ile) | gnomAD v4 |
15 | g.73322487A>C | CA393084607 | HCN4 | c.3606T>G (p.Asn1202Lys) c.2388T>G (p.Asn796Lys) | |
15 | g.73322487A>G | CA491477748 | HCN4 | c.3606T>C (p.Asn1202=) c.2388T>C (p.Asn796=) | |
15 | g.73322487A>T | CA393084608 | HCN4 | c.3606T>A (p.Asn1202Lys) c.2388T>A (p.Asn796Lys) | |
15 | g.73322488T>A | CA393084609 | HCN4 | c.3605A>T (p.Asn1202Ile) c.2387A>T (p.Asn796Ile) | |
15 | g.73322488T>C | CA7648790 | HCN4 | c.3605A>G (p.Asn1202Ser) c.2387A>G (p.Asn796Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322488T>G | CA393084610 | HCN4 | c.3605A>C (p.Asn1202Thr) c.2387A>C (p.Asn796Thr) | |
15 | g.73322488T= | CA2187186022 | HCN4 | c.3605A= (p.Asn1202=) c.2387A= (p.Asn796=) | |
15 | g.73322489T>A | CA393084611 | HCN4 | c.3604A>T (p.Asn1202Tyr) c.2386A>T (p.Asn796Tyr) | gnomAD v4 |
15 | g.73322489T>C | CA393084613 | HCN4 | c.3604A>G (p.Asn1202Asp) c.2386A>G (p.Asn796Asp) | |
15 | g.73322489T>G | CA393084612 | HCN4 | c.3604A>C (p.Asn1202His) c.2386A>C (p.Asn796His) | gnomAD v4 |
15 | g.73322490G>A | CA491477749 | HCN4 | c.3603C>T (p.Ser1201=) c.2385C>T (p.Ser795=) | gnomAD v4 |
15 | g.73322490G>C | CA491477750 | HCN4 | c.3603C>G (p.Ser1201=) c.2385C>G (p.Ser795=) | |
15 | g.73322490G>T | CA491477751 | HCN4 | c.3603C>A (p.Ser1201=) c.2385C>A (p.Ser795=) | gnomAD v4 |
15 | g.73322491G>A | CA393084614 | HCN4 | c.3602C>T (p.Ser1201Phe) c.2384C>T (p.Ser795Phe) | ClinVar dbSNP gnomAD v4 |
15 | g.73322491G>C | CA393084615 | HCN4 | c.3602C>G (p.Ser1201Cys) c.2384C>G (p.Ser795Cys) | |
15 | g.73322491G= | CA2187186026 | HCN4 | c.3602C= (p.Ser1201=) c.2384C= (p.Ser795=) | |
15 | g.73322491G>T | CA393084616 | HCN4 | c.3602C>A (p.Ser1201Tyr) c.2384C>A (p.Ser795Tyr) | COSMIC |
15 | g.73322491_73322493delinsAAC | CA2580613289 | HCN4 | c.3600_3602delinsGTT (p.Ser1201Phe) c.2382_2384delinsGTT (p.Ser795Phe) | ClinVar |
15 | g.73322492A>C | CA393084618 | HCN4 | c.3601T>G (p.Ser1201Ala) c.2383T>G (p.Ser795Ala) | |
15 | g.73322492A>G | CA393084619 | HCN4 | c.3601T>C (p.Ser1201Pro) c.2383T>C (p.Ser795Pro) | |
15 | g.73322492A>T | CA393084621 | HCN4 | c.3601T>A (p.Ser1201Thr) c.2383T>A (p.Ser795Thr) | |
15 | g.73322493T>A | CA7648791 | HCN4 | c.3600A>T (p.Pro1200=) c.2382A>T (p.Pro794=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322493T>C | CA148388 | HCN4 | c.3600A>G (p.Pro1200=) c.2382A>G (p.Pro794=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322493T>G | CA491477752 | HCN4 | c.3600A>C (p.Pro1200=) c.2382A>C (p.Pro794=) | gnomAD v4 |
15 | g.73322493T= | CA2187186037 | HCN4 | c.3600A= (p.Pro1200=) c.2382A= (p.Pro794=) | |
15 | g.73322493_73322494delinsCA | CA891844154 | HCN4 | c.3599_3600delinsTG (p.Pro1200Leu) c.2381_2382delinsTG (p.Pro794Leu) | ClinVar |
15 | g.73322494G>A | CA7648792 | HCN4 | c.3599C>T (p.Pro1200Leu) c.2381C>T (p.Pro794Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322494G>C | CA393084627 | HCN4 | c.3599C>G (p.Pro1200Arg) c.2381C>G (p.Pro794Arg) | |
15 | g.73322494G= | CA2187186049 | HCN4 | c.3599C= (p.Pro1200=) c.2381C= (p.Pro794=) | |
15 | g.73322494G>T | CA7648793 | HCN4 | c.3599C>A (p.Pro1200Gln) c.2381C>A (p.Pro794Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322495del | CA2629370522 | HCN4 | c.3599del (p.Pro1200HisfsTer29) c.2381del (p.Pro794HisfsTer29) | gnomAD v4 |
15 | g.73322495G>A | CA393084631 | HCN4 | c.3598C>T (p.Pro1200Ser) c.2380C>T (p.Pro794Ser) | gnomAD v4 |
15 | g.73322495G>C | CA393084636 | HCN4 | c.3598C>G (p.Pro1200Ala) c.2380C>G (p.Pro794Ala) | gnomAD v4 |
15 | g.73322495G>T | CA393084633 | HCN4 | c.3598C>A (p.Pro1200Thr) c.2380C>A (p.Pro794Thr) | gnomAD v4 |
15 | g.73322496C>A | CA491477753 | HCN4 | c.3597G>T (p.Leu1199=) c.2379G>T (p.Leu793=) | gnomAD v4 |
15 | g.73322496C>G | CA491477754 | HCN4 | c.3597G>C (p.Leu1199=) c.2379G>C (p.Leu793=) | |
15 | g.73322496C>T | CA491477755 | HCN4 | c.3597G>A (p.Leu1199=) c.2379G>A (p.Leu793=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322497A= | CA2187186059 | HCN4 | c.3596T= (p.Leu1199=) c.2378T= (p.Leu793=) | |
15 | g.73322497A>C | CA393084639 | HCN4 | c.3596T>G (p.Leu1199Arg) c.2378T>G (p.Leu793Arg) | |
15 | g.73322497A>G | CA393084642 | HCN4 | c.3596T>C (p.Leu1199Pro) c.2378T>C (p.Leu793Pro) | |
15 | g.73322497A>T | CA272662970 | HCN4 | c.3596T>A (p.Leu1199Gln) c.2378T>A (p.Leu793Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322498G>A | CA491477756 | HCN4 | c.3595C>T (p.Leu1199=) c.2377C>T (p.Leu793=) | |
15 | g.73322498G>C | CA393084645 | HCN4 | c.3595C>G (p.Leu1199Val) c.2377C>G (p.Leu793Val) | |
15 | g.73322498G= | CA2187186066 | HCN4 | c.3595C= (p.Leu1199=) c.2377C= (p.Leu793=) | |
15 | g.73322498G>T | CA7648794 | HCN4 | c.3595C>A (p.Leu1199Met) c.2377C>A (p.Leu793Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322499T>A | CA393084650 | HCN4 | c.3594A>T (p.Lys1198Asn) c.2376A>T (p.Lys792Asn) | |
15 | g.73322499T>C | CA491477757 | HCN4 | c.3594A>G (p.Lys1198=) c.2376A>G (p.Lys792=) | |
15 | g.73322499T>G | CA393084652 | HCN4 | c.3594A>C (p.Lys1198Asn) c.2376A>C (p.Lys792Asn) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322499T= | CA2187186072 | HCN4 | c.3594A= (p.Lys1198=) c.2376A= (p.Lys792=) | |
15 | g.73322500T>A | CA393084655 | HCN4 | c.3593A>T (p.Lys1198Ile) c.2375A>T (p.Lys792Ile) | |
15 | g.73322500T>C | CA393084658 | HCN4 | c.3593A>G (p.Lys1198Arg) c.2375A>G (p.Lys792Arg) | |
15 | g.73322500T>G | CA393084661 | HCN4 | c.3593A>C (p.Lys1198Thr) c.2375A>C (p.Lys792Thr) | gnomAD v4 |
15 | g.73322501T>A | CA393084663 | HCN4 | c.3592A>T (p.Lys1198Ter) c.2374A>T (p.Lys792Ter) | |
15 | g.73322501T>C | CA393084666 | HCN4 | c.3592A>G (p.Lys1198Glu) c.2374A>G (p.Lys792Glu) | gnomAD v4 |
15 | g.73322501T>G | CA393084668 | HCN4 | c.3592A>C (p.Lys1198Gln) c.2374A>C (p.Lys792Gln) | |
15 | g.73322502G>A | CA491477758 | HCN4 | c.3591C>T (p.Ser1197=) c.2373C>T (p.Ser791=) | |
15 | g.73322502G>C | CA491477760 | HCN4 | c.3591C>G (p.Ser1197=) c.2373C>G (p.Ser791=) | |
15 | g.73322502G>T | CA491477759 | HCN4 | c.3591C>A (p.Ser1197=) c.2373C>A (p.Ser791=) | gnomAD v4 |
15 | g.73322503G>A | CA7648796 | HCN4 | c.3590C>T (p.Ser1197Phe) c.2372C>T (p.Ser791Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322503G>C | CA7648795 | HCN4 | c.3590C>G (p.Ser1197Cys) c.2372C>G (p.Ser791Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322503G= | CA2187186076 | HCN4 | c.3590C= (p.Ser1197=) c.2372C= (p.Ser791=) | |
15 | g.73322503G>T | CA393084676 | HCN4 | c.3590C>A (p.Ser1197Tyr) c.2372C>A (p.Ser791Tyr) | gnomAD v4 |
15 | g.73322504A>C | CA393084679 | HCN4 | c.3589T>G (p.Ser1197Ala) c.2371T>G (p.Ser791Ala) | |
15 | g.73322504A>G | CA393084681 | HCN4 | c.3589T>C (p.Ser1197Pro) c.2371T>C (p.Ser791Pro) | gnomAD v4 |
15 | g.73322504A>T | CA393084684 | HCN4 | c.3589T>A (p.Ser1197Thr) c.2371T>A (p.Ser791Thr) | gnomAD v4 |
15 | g.73322505G>A | CA491477813 | HCN4 | c.3588C>T (p.Arg1196=) c.2370C>T (p.Arg790=) | gnomAD v4 |
15 | g.73322505G>C | CA491477815 | HCN4 | c.3588C>G (p.Arg1196=) c.2370C>G (p.Arg790=) | |
15 | g.73322505G>T | CA491477816 | HCN4 | c.3588C>A (p.Arg1196=) c.2370C>A (p.Arg790=) | gnomAD v4 |
15 | g.73322506C>A | CA393084692 | HCN4 | c.3587G>T (p.Arg1196Leu) c.2369G>T (p.Arg790Leu) | gnomAD v4 |
15 | g.73322506C= | CA2187186080 | HCN4 | c.3587G= (p.Arg1196=) c.2369G= (p.Arg790=) | |
15 | g.73322506C>G | CA393084688 | HCN4 | c.3587G>C (p.Arg1196Pro) c.2369G>C (p.Arg790Pro) | |
15 | g.73322506C>T | CA203629 | HCN4 | c.3587G>A (p.Arg1196His) c.2369G>A (p.Arg790His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322507G>A | CA7648797 | HCN4 | c.3586C>T (p.Arg1196Cys) c.2368C>T (p.Arg790Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322507G>C | CA393084696 | HCN4 | c.3586C>G (p.Arg1196Gly) c.2368C>G (p.Arg790Gly) | |
15 | g.73322507G= | CA2187186093 | HCN4 | c.3586C= (p.Arg1196=) c.2368C= (p.Arg790=) | |
15 | g.73322507G>T | CA393084699 | HCN4 | c.3586C>A (p.Arg1196Ser) c.2368C>A (p.Arg790Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.73322508C>A | CA491477819 | HCN4 | c.3585G>T (p.Val1195=) c.2367G>T (p.Val789=) | gnomAD v4 |
15 | g.73322508C>G | CA491477820 | HCN4 | c.3585G>C (p.Val1195=) c.2367G>C (p.Val789=) | |
15 | g.73322508C>T | CA491477821 | HCN4 | c.3585G>A (p.Val1195=) c.2367G>A (p.Val789=) | |
15 | g.73322509A>C | CA393084701 | HCN4 | c.3584T>G (p.Val1195Gly) c.2366T>G (p.Val789Gly) | |
15 | g.73322509A>G | CA393084704 | HCN4 | c.3584T>C (p.Val1195Ala) c.2366T>C (p.Val789Ala) | |
15 | g.73322509A>T | CA393084707 | HCN4 | c.3584T>A (p.Val1195Glu) c.2366T>A (p.Val789Glu) | gnomAD v4 |
15 | g.73322510C>A | CA7648798 | HCN4 | c.3583G>T (p.Val1195Leu) c.2365G>T (p.Val789Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322510C= | CA2187186098 | HCN4 | c.3583G= (p.Val1195=) c.2365G= (p.Val789=) | |
15 | g.73322510C>G | CA393084711 | HCN4 | c.3583G>C (p.Val1195Leu) c.2365G>C (p.Val789Leu) | |
15 | g.73322510C>T | CA393084714 | HCN4 | c.3583G>A (p.Val1195Met) c.2365G>A (p.Val789Met) | gnomAD v4 |
15 | g.73322511T>A | CA491477824 | HCN4 | c.3582A>T (p.Pro1194=) c.2364A>T (p.Pro788=) | |
15 | g.73322511T>C | CA7648799 | HCN4 | c.3582A>G (p.Pro1194=) c.2364A>G (p.Pro788=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322511T>G | CA491477825 | HCN4 | c.3582A>C (p.Pro1194=) c.2364A>C (p.Pro788=) | |
15 | g.73322511T= | CA2187186104 | HCN4 | c.3582A= (p.Pro1194=) c.2364A= (p.Pro788=) | |
15 | g.73322512G>A | CA7648800 | HCN4 | c.3581C>T (p.Pro1194Leu) c.2363C>T (p.Pro788Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322512G>C | CA393084720 | HCN4 | c.3581C>G (p.Pro1194Arg) c.2363C>G (p.Pro788Arg) | |
15 | g.73322512G= | CA2187186109 | HCN4 | c.3581C= (p.Pro1194=) c.2363C= (p.Pro788=) | |
15 | g.73322512G>T | CA393084719 | HCN4 | c.3581C>A (p.Pro1194Gln) c.2363C>A (p.Pro788Gln) | gnomAD v4 |
15 | g.73322513G>A | CA393084725 | HCN4 | c.3580C>T (p.Pro1194Ser) c.2362C>T (p.Pro788Ser) | gnomAD v4 |
15 | g.73322513G>C | CA393084726 | HCN4 | c.3580C>G (p.Pro1194Ala) c.2362C>G (p.Pro788Ala) | |
15 | g.73322513G>T | CA393084728 | HCN4 | c.3580C>A (p.Pro1194Thr) c.2362C>A (p.Pro788Thr) | gnomAD v4 |
15 | g.73322514C>A | CA393084731 | HCN4 | c.3579G>T (p.Glu1193Asp) c.2361G>T (p.Glu787Asp) | |
15 | g.73322514C= | CA2187186111 | HCN4 | c.3579G= (p.Glu1193=) c.2361G= (p.Glu787=) | |
15 | g.73322514C>G | CA393084734 | HCN4 | c.3579G>C (p.Glu1193Asp) c.2361G>C (p.Glu787Asp) | |
15 | g.73322514C>T | CA491477830 | HCN4 | c.3579G>A (p.Glu1193=) c.2361G>A (p.Glu787=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322515T>A | CA393084737 | HCN4 | c.3578A>T (p.Glu1193Val) c.2360A>T (p.Glu787Val) | |
15 | g.73322515T>C | CA393084740 | HCN4 | c.3578A>G (p.Glu1193Gly) c.2360A>G (p.Glu787Gly) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322515T>G | CA393084742 | HCN4 | c.3578A>C (p.Glu1193Ala) c.2360A>C (p.Glu787Ala) | |
15 | g.73322515T= | CA2187186117 | HCN4 | c.3578A= (p.Glu1193=) c.2360A= (p.Glu787=) | |
15 | g.73322516C>A | CA7648801 | HCN4 | c.3577G>T (p.Glu1193Ter) c.2359G>T (p.Glu787Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322516C= | CA2187186128 | HCN4 | c.3577G= (p.Glu1193=) c.2359G= (p.Glu787=) | |
15 | g.73322516C>G | CA236695 | HCN4 | c.3577G>C (p.Glu1193Gln) c.2359G>C (p.Glu787Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322516C>T | CA393084748 | HCN4 | c.3577G>A (p.Glu1193Lys) c.2359G>A (p.Glu787Lys) | gnomAD v4 |
15 | g.73322517A>C | CA491477832 | HCN4 | c.3576T>G (p.Pro1192=) c.2358T>G (p.Pro786=) | |
15 | g.73322517A>G | CA491477833 | HCN4 | c.3576T>C (p.Pro1192=) c.2358T>C (p.Pro786=) | |
15 | g.73322517A>T | CA491477834 | HCN4 | c.3576T>A (p.Pro1192=) c.2358T>A (p.Pro786=) | |
15 | g.73322518G>A | CA7648802 | HCN4 | c.3575C>T (p.Pro1192Leu) c.2357C>T (p.Pro786Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322518G>C | CA393084754 | HCN4 | c.3575C>G (p.Pro1192Arg) c.2357C>G (p.Pro786Arg) | ClinVar |
15 | g.73322518G= | CA2187186131 | HCN4 | c.3575C= (p.Pro1192=) c.2357C= (p.Pro786=) | |
15 | g.73322518G>T | CA393084751 | HCN4 | c.3575C>A (p.Pro1192His) c.2357C>A (p.Pro786His) | gnomAD v4 |
15 | g.73322519G>A | CA7648803 | HCN4 | c.3574C>T (p.Pro1192Ser) c.2356C>T (p.Pro786Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322519G>C | CA393084759 | HCN4 | c.3574C>G (p.Pro1192Ala) c.2356C>G (p.Pro786Ala) | gnomAD v4 |
15 | g.73322519G= | CA2187186138 | HCN4 | c.3574C= (p.Pro1192=) c.2356C= (p.Pro786=) | |
15 | g.73322519G>T | CA393084761 | HCN4 | c.3574C>A (p.Pro1192Thr) c.2356C>A (p.Pro786Thr) | gnomAD v4 |
15 | g.73322520C>A | CA393084764 | HCN4 | c.3573G>T (p.Arg1191Ser) c.2355G>T (p.Arg785Ser) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322520C= | CA2187186142 | HCN4 | c.3573G= (p.Arg1191=) c.2355G= (p.Arg785=) | |
15 | g.73322520C>G | CA393084767 | HCN4 | c.3573G>C (p.Arg1191Ser) c.2355G>C (p.Arg785Ser) | |
15 | g.73322520C>T | CA491477837 | HCN4 | c.3573G>A (p.Arg1191=) c.2355G>A (p.Arg785=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322521C>A | CA393084769 | HCN4 | c.3572G>T (p.Arg1191Met) c.2354G>T (p.Arg785Met) | gnomAD v4 |
15 | g.73322521C= | CA2187186145 | HCN4 | c.3572G= (p.Arg1191=) c.2354G= (p.Arg785=) | |
15 | g.73322521C>G | CA393084772 | HCN4 | c.3572G>C (p.Arg1191Thr) c.2354G>C (p.Arg785Thr) | dbSNP gnomAD v4 |
15 | g.73322521C>T | CA393084774 | HCN4 | c.3572G>A (p.Arg1191Lys) c.2354G>A (p.Arg785Lys) | gnomAD v4 |
15 | g.73322522T>A | CA393084776 | HCN4 | c.3571A>T (p.Arg1191Trp) c.2353A>T (p.Arg785Trp) | |
15 | g.73322522T>C | CA393084777 | HCN4 | c.3571A>G (p.Arg1191Gly) c.2353A>G (p.Arg785Gly) | dbSNP gnomAD v4 |
15 | g.73322522T>G | CA491477839 | HCN4 | c.3571A>C (p.Arg1191=) c.2353A>C (p.Arg785=) | |
15 | g.73322522T= | CA2187186149 | HCN4 | c.3571A= (p.Arg1191=) c.2353A= (p.Arg785=) | |
15 | g.73322523G>A | CA491477840 | HCN4 | c.3570C>T (p.Ala1190=) c.2352C>T (p.Ala784=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322523G>C | CA491477841 | HCN4 | c.3570C>G (p.Ala1190=) c.2352C>G (p.Ala784=) | |
15 | g.73322523G>T | CA491477842 | HCN4 | c.3570C>A (p.Ala1190=) c.2352C>A (p.Ala784=) | |
15 | g.73322524G>A | CA393084780 | HCN4 | c.3569C>T (p.Ala1190Val) c.2351C>T (p.Ala784Val) | gnomAD v4 |
15 | g.73322524G>C | CA393084783 | HCN4 | c.3569C>G (p.Ala1190Gly) c.2351C>G (p.Ala784Gly) | |
15 | g.73322524G>T | CA393084786 | HCN4 | c.3569C>A (p.Ala1190Asp) c.2351C>A (p.Ala784Asp) | gnomAD v4 |
15 | g.73322525C>A | CA393084787 | HCN4 | c.3568G>T (p.Ala1190Ser) c.2350G>T (p.Ala784Ser) | ClinVar gnomAD v4 |
15 | g.73322525C= | CA2187186155 | HCN4 | c.3568G= (p.Ala1190=) c.2350G= (p.Ala784=) | |
15 | g.73322525C>G | CA393084790 | HCN4 | c.3568G>C (p.Ala1190Pro) c.2350G>C (p.Ala784Pro) | |
15 | g.73322525C>T | CA16614725 | HCN4 | c.3568G>A (p.Ala1190Thr) c.2350G>A (p.Ala784Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322526C>A | CA491477844 | HCN4 | c.3567G>T (p.Gly1189=) c.2349G>T (p.Gly783=) | gnomAD v4 |
15 | g.73322526C= | CA2187186158 | HCN4 | c.3567G= (p.Gly1189=) c.2349G= (p.Gly783=) | |
15 | g.73322526C>G | CA491477845 | HCN4 | c.3567G>C (p.Gly1189=) c.2349G>C (p.Gly783=) | gnomAD v4 |
15 | g.73322526C>T | CA7648804 | HCN4 | c.3567G>A (p.Gly1189=) c.2349G>A (p.Gly783=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322527C>A | CA393084794 | HCN4 | c.3566G>T (p.Gly1189Val) c.2348G>T (p.Gly783Val) | gnomAD v4 |
15 | g.73322527C= | CA2187186161 | HCN4 | c.3566G= (p.Gly1189=) c.2348G= (p.Gly783=) | |
15 | g.73322527C>G | CA393084797 | HCN4 | c.3566G>C (p.Gly1189Ala) c.2348G>C (p.Gly783Ala) | |
15 | g.73322527C>T | CA393084800 | HCN4 | c.3566G>A (p.Gly1189Glu) c.2348G>A (p.Gly783Glu) | dbSNP gnomAD v2 |
15 | g.73322528C>A | CA393084804 | HCN4 | c.3565G>T (p.Gly1189Trp) c.2347G>T (p.Gly783Trp) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322528C= | CA2187186164 | HCN4 | c.3565G= (p.Gly1189=) c.2347G= (p.Gly783=) | |
15 | g.73322528C>G | CA393084806 | HCN4 | c.3565G>C (p.Gly1189Arg) c.2347G>C (p.Gly783Arg) | |
15 | g.73322528C>T | CA393084810 | HCN4 | c.3565G>A (p.Gly1189Arg) c.2347G>A (p.Gly783Arg) | |
15 | g.73322529A>C | CA491477851 | HCN4 | c.3564T>G (p.Pro1188=) c.2346T>G (p.Pro782=) | |
15 | g.73322529A>G | CA491477849 | HCN4 | c.3564T>C (p.Pro1188=) c.2346T>C (p.Pro782=) | ClinVar |
15 | g.73322529A>T | CA491477850 | HCN4 | c.3564T>A (p.Pro1188=) c.2346T>A (p.Pro782=) | |
15 | g.73322530G>A | CA393084813 | HCN4 | c.3563C>T (p.Pro1188Leu) c.2345C>T (p.Pro782Leu) | COSMIC |
15 | g.73322530G>C | CA393084815 | HCN4 | c.3563C>G (p.Pro1188Arg) c.2345C>G (p.Pro782Arg) | gnomAD v4 |
15 | g.73322530G>T | CA393084816 | HCN4 | c.3563C>A (p.Pro1188His) c.2345C>A (p.Pro782His) | |
15 | g.73322531G>A | CA393084819 | HCN4 | c.3562C>T (p.Pro1188Ser) c.2344C>T (p.Pro782Ser) | |
15 | g.73322531G>C | CA393084821 | HCN4 | c.3562C>G (p.Pro1188Ala) c.2344C>G (p.Pro782Ala) | |
15 | g.73322531G>T | CA393084824 | HCN4 | c.3562C>A (p.Pro1188Thr) c.2344C>A (p.Pro782Thr) | gnomAD v4 |
15 | g.73322532T>A | CA393084828 | HCN4 | c.3561A>T (p.Glu1187Asp) c.2343A>T (p.Glu781Asp) | |
15 | g.73322532T>C | CA491477855 | HCN4 | c.3561A>G (p.Glu1187=) c.2343A>G (p.Glu781=) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322532T>G | CA393084825 | HCN4 | c.3561A>C (p.Glu1187Asp) c.2343A>C (p.Glu781Asp) | |
15 | g.73322532T= | CA2187186167 | HCN4 | c.3561A= (p.Glu1187=) c.2343A= (p.Glu781=) | |
15 | g.73322533T>A | CA393084831 | HCN4 | c.3560A>T (p.Glu1187Val) c.2342A>T (p.Glu781Val) | |
15 | g.73322533T>C | CA393084834 | HCN4 | c.3560A>G (p.Glu1187Gly) c.2342A>G (p.Glu781Gly) | |
15 | g.73322533T>G | CA393084835 | HCN4 | c.3560A>C (p.Glu1187Ala) c.2342A>C (p.Glu781Ala) | |
15 | g.73322534C>A | CA393084839 | HCN4 | c.3559G>T (p.Glu1187Ter) c.2341G>T (p.Glu781Ter) | |
15 | g.73322534C>G | CA393084842 | HCN4 | c.3559G>C (p.Glu1187Gln) c.2341G>C (p.Glu781Gln) | |
15 | g.73322534C>T | CA393084844 | HCN4 | c.3559G>A (p.Glu1187Lys) c.2341G>A (p.Glu781Lys) | |
15 | g.73322535C>A | CA393084849 | HCN4 | c.3558G>T (p.Arg1186Ser) c.2340G>T (p.Arg780Ser) | |
15 | g.73322535C>G | CA393084850 | HCN4 | c.3558G>C (p.Arg1186Ser) c.2340G>C (p.Arg780Ser) | |
15 | g.73322535C>T | CA491477858 | HCN4 | c.3558G>A (p.Arg1186=) c.2340G>A (p.Arg780=) | ClinVar gnomAD v4 |
15 | g.73322536C>A | CA393084851 | HCN4 | c.3557G>T (p.Arg1186Met) c.2339G>T (p.Arg780Met) | |
15 | g.73322536C= | CA2187186169 | HCN4 | c.3557G= (p.Arg1186=) c.2339G= (p.Arg780=) | |
15 | g.73322536C>G | CA393084853 | HCN4 | c.3557G>C (p.Arg1186Thr) c.2339G>C (p.Arg780Thr) | |
15 | g.73322536C>T | CA393084855 | HCN4 | c.3557G>A (p.Arg1186Lys) c.2339G>A (p.Arg780Lys) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322537T>A | CA393084858 | HCN4 | c.3556A>T (p.Arg1186Trp) c.2338A>T (p.Arg780Trp) | |
15 | g.73322537T>C | CA393084859 | HCN4 | c.3556A>G (p.Arg1186Gly) c.2338A>G (p.Arg780Gly) | |
15 | g.73322537T>G | CA491477862 | HCN4 | c.3556A>C (p.Arg1186=) c.2338A>C (p.Arg780=) | |
15 | g.73322538C>A | CA393084867 | HCN4 | c.3555G>T (p.Gln1185His) c.2337G>T (p.Gln779His) | gnomAD v4 |
15 | g.73322538C>G | CA393084864 | HCN4 | c.3555G>C (p.Gln1185His) c.2337G>C (p.Gln779His) | |
15 | g.73322538C>T | CA491477863 | HCN4 | c.3555G>A (p.Gln1185=) c.2337G>A (p.Gln779=) | ClinVar gnomAD v4 |
15 | g.73322539T>A | CA393084870 | HCN4 | c.3554A>T (p.Gln1185Leu) c.2336A>T (p.Gln779Leu) | dbSNP |
15 | g.73322539T>C | CA393084871 | HCN4 | c.3554A>G (p.Gln1185Arg) c.2336A>G (p.Gln779Arg) | |
15 | g.73322539T>G | CA393084873 | HCN4 | c.3554A>C (p.Gln1185Pro) c.2336A>C (p.Gln779Pro) | |
15 | g.73322539T= | CA2187186172 | HCN4 | c.3554A= (p.Gln1185=) c.2336A= (p.Gln779=) | |
15 | g.73322540G>A | CA393084876 | HCN4 | c.3553C>T (p.Gln1185Ter) c.2335C>T (p.Gln779Ter) | |
15 | g.73322540G>C | CA393084879 | HCN4 | c.3553C>G (p.Gln1185Glu) c.2335C>G (p.Gln779Glu) | |
15 | g.73322540G>T | CA393084882 | HCN4 | c.3553C>A (p.Gln1185Lys) c.2335C>A (p.Gln779Lys) | gnomAD v4 |
15 | g.73322541G>A | CA491477866 | HCN4 | c.3552C>T (p.Pro1184=) c.2334C>T (p.Pro778=) | dbSNP gnomAD v2 |
15 | g.73322541G>C | CA491477867 | HCN4 | c.3552C>G (p.Pro1184=) c.2334C>G (p.Pro778=) | |
15 | g.73322541G= | CA2187186175 | HCN4 | c.3552C= (p.Pro1184=) c.2334C= (p.Pro778=) | |
15 | g.73322541G>T | CA491477868 | HCN4 | c.3552C>A (p.Pro1184=) c.2334C>A (p.Pro778=) | |
15 | g.73322542G>A | CA393084890 | HCN4 | c.3551C>T (p.Pro1184Leu) c.2333C>T (p.Pro778Leu) | dbSNP |
15 | g.73322542G>C | CA393084887 | HCN4 | c.3551C>G (p.Pro1184Arg) c.2333C>G (p.Pro778Arg) | ClinVar dbSNP gnomAD v4 |
15 | g.73322542G= | CA2187186183 | HCN4 | c.3551C= (p.Pro1184=) c.2333C= (p.Pro778=) | |
15 | g.73322542G>T | CA393084884 | HCN4 | c.3551C>A (p.Pro1184His) c.2333C>A (p.Pro778His) | gnomAD v4 |
15 | g.73322543G>A | CA393084893 | HCN4 | c.3550C>T (p.Pro1184Ser) c.2332C>T (p.Pro778Ser) | gnomAD v4 COSMIC |
15 | g.73322543G>C | CA393084895 | HCN4 | c.3550C>G (p.Pro1184Ala) c.2332C>G (p.Pro778Ala) | ClinVar |
15 | g.73322543G= | CA2187186186 | HCN4 | c.3550C= (p.Pro1184=) c.2332C= (p.Pro778=) | |
15 | g.73322543G>T | CA272663044 | HCN4 | c.3550C>A (p.Pro1184Thr) c.2332C>A (p.Pro778Thr) | dbSNP gnomAD v4 |
15 | g.73322544T>A | CA491477872 | HCN4 | c.3549A>T (p.Gly1183=) c.2331A>T (p.Gly777=) | |
15 | g.73322544T>C | CA491477873 | HCN4 | c.3549A>G (p.Gly1183=) c.2331A>G (p.Gly777=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322544T>G | CA491477874 | HCN4 | c.3549A>C (p.Gly1183=) c.2331A>C (p.Gly777=) | |
15 | g.73322544T= | CA2187186189 | HCN4 | c.3549A= (p.Gly1183=) c.2331A= (p.Gly777=) |