UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73324030G>A | CA272665293 | HCN4 | c.2143+59C>T (n.2143+59C>T) c.925+59C>T (n.925+59C>T) | dbSNP gnomAD v4 |
| 15 | g.73324030G>C | CA2629370928 | HCN4 | c.2143+59C>G (n.2143+59C>G) c.925+59C>G (n.925+59C>G) | gnomAD v4 |
| 15 | g.73324030G= | CA2187188907 | HCN4 | c.2143+59C= (n.2143+59C=) c.925+59C= (n.925+59C=) | |
| 15 | g.73324030G>T | CA2629370929 | HCN4 | c.2143+59C>A (n.2143+59C>A) c.925+59C>A (n.925+59C>A) | gnomAD v4 |
| 15 | g.73324031C>A | CA2629370930 | HCN4 | c.2143+58G>T (n.2143+58G>T) c.925+58G>T (n.925+58G>T) | gnomAD v4 |
| 15 | g.73324031C= | CA2187188908 | HCN4 | c.2143+58G= (n.2143+58G=) c.925+58G= (n.925+58G=) | |
| 15 | g.73324031C>G | CA2187188909 | HCN4 | c.2143+58G>C (n.2143+58G>C) c.925+58G>C (n.925+58G>C) | dbSNP |
| 15 | g.73324031C>T | CA715546931 | HCN4 | c.2143+58G>A (n.2143+58G>A) c.925+58G>A (n.925+58G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324033C>A | CA2575783844 | HCN4 | c.2143+56G>T (n.2143+56G>T) c.925+56G>T (n.925+56G>T) | gnomAD v4 |
| 15 | g.73324034T>C | CA2629370931 | HCN4 | c.2143+55A>G (n.2143+55A>G) c.925+55A>G (n.925+55A>G) | gnomAD v4 |
| 15 | g.73324035G>A | CA2629370932 | HCN4 | c.2143+54C>T (n.2143+54C>T) c.925+54C>T (n.925+54C>T) | gnomAD v4 |
| 15 | g.73324035G>T | CA2629370933 | HCN4 | c.2143+54C>A (n.2143+54C>A) c.925+54C>A (n.925+54C>A) | dbSNP gnomAD v4 |
| 15 | g.73324036C>T | CA2629370934 | HCN4 | c.2143+53G>A (n.2143+53G>A) c.925+53G>A (n.925+53G>A) | gnomAD v4 |
| 15 | g.73324038dup | CA2629370935 | HCN4 | c.2143+53dup (n.2143+53dup) c.925+53dup (n.925+53dup) | gnomAD v4 |
| 15 | g.73324038C>A | CA2629370936 | HCN4 | c.2143+51G>T (n.2143+51G>T) c.925+51G>T (n.925+51G>T) | gnomAD v4 |
| 15 | g.73324038C= | CA2187188910 | HCN4 | c.2143+51G= (n.2143+51G=) c.925+51G= (n.925+51G=) | |
| 15 | g.73324038C>T | CA619410617 | HCN4 | c.2143+51G>A (n.2143+51G>A) c.925+51G>A (n.925+51G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324039T>A | CA2629370937 | HCN4 | c.2143+50A>T (n.2143+50A>T) c.925+50A>T (n.925+50A>T) | gnomAD v4 |
| 15 | g.73324039T>C | CA971395216 | HCN4 | c.2143+50A>G (n.2143+50A>G) c.925+50A>G (n.925+50A>G) | gnomAD v3 gnomAD v4 |
| 15 | g.73324041C>T | CA2629370938 | HCN4 | c.2143+48G>A (n.2143+48G>A) c.925+48G>A (n.925+48G>A) | gnomAD v4 |
| 15 | g.73324042T>A | CA2595918353 | HCN4 | c.2143+47A>T (n.2143+47A>T) c.925+47A>T (n.925+47A>T) | gnomAD v3 gnomAD v4 |
| 15 | g.73324042T>C | CA619410594 | HCN4 | c.2143+47A>G (n.2143+47A>G) c.925+47A>G (n.925+47A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324042T= | CA2187188911 | HCN4 | c.2143+47A= (n.2143+47A=) c.925+47A= (n.925+47A=) | |
| 15 | g.73324043C= | CA2187188912 | HCN4 | c.2143+46G= (n.2143+46G=) c.925+46G= (n.925+46G=) | |
| 15 | g.73324043C>G | CA2187188913 | HCN4 | c.2143+46G>C (n.2143+46G>C) c.925+46G>C (n.925+46G>C) | dbSNP |
| 15 | g.73324047dup | CA619410595 | HCN4 | c.2143+46dup (n.2143+46dup) c.925+46dup (n.925+46dup) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324047del | CA2629370939 | HCN4 | c.2143+46del (n.2143+46del) c.925+46del (n.925+46del) | gnomAD v4 |
| 15 | g.73324044C>A | CA2629370940 | HCN4 | c.2143+45G>T (n.2143+45G>T) c.925+45G>T (n.925+45G>T) | gnomAD v4 |
| 15 | g.73324045C= | CA2187188914 | HCN4 | c.2143+44G= (n.2143+44G=) c.925+44G= (n.925+44G=) | |
| 15 | g.73324045C>T | CA7649102 | HCN4 | c.2143+44G>A (n.2143+44G>A) c.925+44G>A (n.925+44G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324046C>A | CA2575783845 | HCN4 | c.2143+43G>T (n.2143+43G>T) c.925+43G>T (n.925+43G>T) | gnomAD v4 |
| 15 | g.73324046C>G | CA2804714161 | HCN4 | c.2143+43G>C (n.2143+43G>C) c.925+43G>C (n.925+43G>C) | |
| 15 | g.73324046C>T | CA2571121417 | HCN4 | c.2143+43G>A (n.2143+43G>A) c.925+43G>A (n.925+43G>A) | |
| 15 | g.73324047C>A | CA2804714162 | HCN4 | c.2143+42G>T (n.2143+42G>T) c.925+42G>T (n.925+42G>T) | |
| 15 | g.73324047C= | CA2187188915 | HCN4 | c.2143+42G= (n.2143+42G=) c.925+42G= (n.925+42G=) | |
| 15 | g.73324048A= | CA2187188917 | HCN4 | c.2143+41T= (n.2143+41T=) c.925+41T= (n.925+41T=) | |
| 15 | g.73324048A>C | CA619410596 | HCN4 | c.2143+41T>G (n.2143+41T>G) c.925+41T>G (n.925+41T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324048A>G | CA2187188919 | HCN4 | c.2143+41T>C (n.2143+41T>C) c.925+41T>C (n.925+41T>C) | dbSNP gnomAD v4 |
| 15 | g.73324048_73324049del | CA2575783846 | HCN4 | c.2143+40_2143+41del (n.2143+40_2143+41del) c.925+40_925+41del (n.925+40_925+41del) | |
| 15 | g.73324048_73324051dup | CA2187188916 | HCN4 | c.2143+38_2143+41dup (n.2143+38_2143+41dup) c.925+38_925+41dup (n.925+38_925+41dup) | dbSNP gnomAD v4 |
| 15 | g.73324048_73324049insCAACCCAAAC | CA2804714163 | HCN4 | c.2143+40_2143+41insGTTTGGGTTG (n.2143+40_2143+41insGTTTGGGTTG) c.925+40_925+41insGTTTGGGTTG (n.925+40_925+41insGTTTGGGTTG) | |
| 15 | g.73324049A= | CA2187188920 | HCN4 | c.2143+40T= (n.2143+40T=) c.925+40T= (n.925+40T=) | |
| 15 | g.73324049A>C | CA2629370941 | HCN4 | c.2143+40T>G (n.2143+40T>G) c.925+40T>G (n.925+40T>G) | gnomAD v4 |
| 15 | g.73324049A>G | CA7649103 | HCN4 | c.2143+40T>C (n.2143+40T>C) c.925+40T>C (n.925+40T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324050C>A | CA2629370942 | HCN4 | c.2143+39G>T (n.2143+39G>T) c.925+39G>T (n.925+39G>T) | gnomAD v4 |
| 15 | g.73324051A= | CA2187188922 | HCN4 | c.2143+38T= (n.2143+38T=) c.925+38T= (n.925+38T=) | |
| 15 | g.73324051A>C | CA7649104 | HCN4 | c.2143+38T>G (n.2143+38T>G) c.925+38T>G (n.925+38T>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324051_73324052delinsAC | CA2187188921 | HCN4 | c.2143+37_2143+38delinsGT (n.2143+37_2143+38delinsGT) c.925+37_925+38delinsGT (n.925+37_925+38delinsGT) | |
| 15 | g.73324052C>A | CA7649106 | HCN4 | c.2143+37G>T (n.2143+37G>T) c.925+37G>T (n.925+37G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324052C= | CA2187188925 | HCN4 | c.2143+37G= (n.2143+37G=) c.925+37G= (n.925+37G=) | |
| 15 | g.73324052C>T | CA2629370944 | HCN4 | c.2143+37G>A (n.2143+37G>A) c.925+37G>A (n.925+37G>A) | gnomAD v4 |
| 15 | g.73324057dup | CA2629370943 | HCN4 | c.2143+37dup (n.2143+37dup) c.925+37dup (n.925+37dup) | gnomAD v4 |
| 15 | g.73324057del | CA7649105 | HCN4 | c.2143+37del (n.2143+37del) c.925+37del (n.925+37del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324056_73324057del | CA2804714164 | HCN4 | c.2143+36_2143+37del (n.2143+36_2143+37del) c.925+36_925+37del (n.925+36_925+37del) | |
| 15 | g.73324053C>A | CA619410597 | HCN4 | c.2143+36G>T (n.2143+36G>T) c.925+36G>T (n.925+36G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324053C= | CA2187188927 | HCN4 | c.2143+36G= (n.2143+36G=) c.925+36G= (n.925+36G=) | |
| 15 | g.73324053C>T | CA2629370945 | HCN4 | c.2143+36G>A (n.2143+36G>A) c.925+36G>A (n.925+36G>A) | gnomAD v4 |
| 15 | g.73324054C>A | CA2629370946 | HCN4 | c.2143+35G>T (n.2143+35G>T) c.925+35G>T (n.925+35G>T) | gnomAD v4 |
| 15 | g.73324054C= | CA2187188929 | HCN4 | c.2143+35G= (n.2143+35G=) c.925+35G= (n.925+35G=) | |
| 15 | g.73324054C>G | CA7649107 | HCN4 | c.2143+35G>C (n.2143+35G>C) c.925+35G>C (n.925+35G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324054C>T | CA2629370947 | HCN4 | c.2143+35G>A (n.2143+35G>A) c.925+35G>A (n.925+35G>A) | gnomAD v4 |
| 15 | g.73324054_73324055insAAACACA | CA2804714165 | HCN4 | c.2143+34_2143+35insTGTGTTT (n.2143+34_2143+35insTGTGTTT) c.925+34_925+35insTGTGTTT (n.925+34_925+35insTGTGTTT) | |
| 15 | g.73324055C>A | CA7649108 | HCN4 | c.2143+34G>T (n.2143+34G>T) c.925+34G>T (n.925+34G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324055C= | CA2187188932 | HCN4 | c.2143+34G= (n.2143+34G=) c.925+34G= (n.925+34G=) | |
| 15 | g.73324055C>G | CA715546948 | HCN4 | c.2143+34G>C (n.2143+34G>C) c.925+34G>C (n.925+34G>C) | dbSNP |
| 15 | g.73324055C>T | CA272665319 | HCN4 | c.2143+34G>A (n.2143+34G>A) c.925+34G>A (n.925+34G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324056C>A | CA715546953 | HCN4 | c.2143+33G>T (n.2143+33G>T) c.925+33G>T (n.925+33G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324056C= | CA2187188934 | HCN4 | c.2143+33G= (n.2143+33G=) c.925+33G= (n.925+33G=) | |
| 15 | g.73324056C>T | CA2629370948 | HCN4 | c.2143+33G>A (n.2143+33G>A) c.925+33G>A (n.925+33G>A) | gnomAD v4 |
| 15 | g.73324056_73324057insAACA | CA2804714166 | HCN4 | c.2143+32_2143+33insTGTT (n.2143+32_2143+33insTGTT) c.925+32_925+33insTGTT (n.925+32_925+33insTGTT) | |
| 15 | g.73324057C>A | CA272665322 | HCN4 | c.2143+32G>T (n.2143+32G>T) c.925+32G>T (n.925+32G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324057C= | CA2187188937 | HCN4 | c.2143+32G= (n.2143+32G=) c.925+32G= (n.925+32G=) | |
| 15 | g.73324057C>G | CA7649109 | HCN4 | c.2143+32G>C (n.2143+32G>C) c.925+32G>C (n.925+32G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324057C>T | CA619410598 | HCN4 | c.2143+32G>A (n.2143+32G>A) c.925+32G>A (n.925+32G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324058_73324059insACACA | CA2804714167 | HCN4 | c.2143+32_2143+33insTGTTG (n.2143+32_2143+33insTGTTG) c.925+32_925+33insTGTTG (n.925+32_925+33insTGTTG) | |
| 15 | g.73324058A= | CA2187188940 | HCN4 | c.2143+31T= (n.2143+31T=) c.925+31T= (n.925+31T=) | |
| 15 | g.73324058A>C | CA7649110 | HCN4 | c.2143+31T>G (n.2143+31T>G) c.925+31T>G (n.925+31T>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324058_73324074del | CA2629370949 | HCN4 | c.2143+15_2143+31del (n.2143+15_2143+31del) c.925+15_925+31del (n.925+15_925+31del) | gnomAD v4 |
| 15 | g.73324059C>A | CA2187188945 | HCN4 | c.2143+30G>T (n.2143+30G>T) c.925+30G>T (n.925+30G>T) | dbSNP |
| 15 | g.73324059C= | CA2187188942 | HCN4 | c.2143+30G= (n.2143+30G=) c.925+30G= (n.925+30G=) | |
| 15 | g.73324059C>G | CA619410599 | HCN4 | c.2143+30G>C (n.2143+30G>C) c.925+30G>C (n.925+30G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324059C>T | CA2187188944 | HCN4 | c.2143+30G>A (n.2143+30G>A) c.925+30G>A (n.925+30G>A) | dbSNP |
| 15 | g.73324060C>G | CA2629370950 | HCN4 | c.2143+29G>C (n.2143+29G>C) c.925+29G>C (n.925+29G>C) | gnomAD v4 |
| 15 | g.73324061T>A | CA971395235 | HCN4 | c.2143+28A>T (n.2143+28A>T) c.925+28A>T (n.925+28A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324061T>C | CA914026804 | HCN4 | c.2143+28A>G (n.2143+28A>G) c.925+28A>G (n.925+28A>G) | gnomAD v2 gnomAD v4 |
| 15 | g.73324061T>G | CA7649111 | HCN4 | c.2143+28A>C (n.2143+28A>C) c.925+28A>C (n.925+28A>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324061T= | CA2187188947 | HCN4 | c.2143+28A= (n.2143+28A=) c.925+28A= (n.925+28A=) | |
| 15 | g.73324062G>A | CA715546960 | HCN4 | c.2143+27C>T (n.2143+27C>T) c.925+27C>T (n.925+27C>T) | dbSNP |
| 15 | g.73324062G= | CA2187188949 | HCN4 | c.2143+27C= (n.2143+27C=) c.925+27C= (n.925+27C=) | |
| 15 | g.73324062G>T | CA7649112 | HCN4 | c.2143+27C>A (n.2143+27C>A) c.925+27C>A (n.925+27C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324063C>A | CA2575783847 | HCN4 | c.2143+26G>T (n.2143+26G>T) c.925+26G>T (n.925+26G>T) | |
| 15 | g.73324064C>A | CA2629370951 | HCN4 | c.2143+25G>T (n.2143+25G>T) c.925+25G>T (n.925+25G>T) | gnomAD v4 |
| 15 | g.73324064C>T | CA656217074 | HCN4 | c.2143+25G>A (n.2143+25G>A) c.925+25G>A (n.925+25G>A) | COSMIC |
| 15 | g.73324065C>A | CA2575783848 | HCN4 | c.2143+24G>T (n.2143+24G>T) c.925+24G>T (n.925+24G>T) | |
| 15 | g.73324065C= | CA2187188950 | HCN4 | c.2143+24G= (n.2143+24G=) c.925+24G= (n.925+24G=) | |
| 15 | g.73324065C>T | CA715546963 | HCN4 | c.2143+24G>A (n.2143+24G>A) c.925+24G>A (n.925+24G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324066C= | CA2187188952 | HCN4 | c.2143+23G= (n.2143+23G=) c.925+23G= (n.925+23G=) | |
| 15 | g.73324066C>G | CA272665336 | HCN4 | c.2143+23G>C (n.2143+23G>C) c.925+23G>C (n.925+23G>C) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324066C>T | CA7649113 | HCN4 | c.2143+23G>A (n.2143+23G>A) c.925+23G>A (n.925+23G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324067G>A | CA7649114 | HCN4 | c.2143+22C>T (n.2143+22C>T) c.925+22C>T (n.925+22C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324067G>C | CA971395240 | HCN4 | c.2143+22C>G (n.2143+22C>G) c.925+22C>G (n.925+22C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324067G= | CA2187188955 | HCN4 | c.2143+22C= (n.2143+22C=) c.925+22C= (n.925+22C=) | |
| 15 | g.73324068C>A | CA2187188959 | HCN4 | c.2143+21G>T (n.2143+21G>T) c.925+21G>T (n.925+21G>T) | dbSNP |
| 15 | g.73324068C= | CA2187188958 | HCN4 | c.2143+21G= (n.2143+21G=) c.925+21G= (n.925+21G=) | |
| 15 | g.73324069C>T | CA2629370952 | HCN4 | c.2143+20G>A (n.2143+20G>A) c.925+20G>A (n.925+20G>A) | gnomAD v4 |
| 15 | g.73324070T>A | CA971395244 | HCN4 | c.2143+19A>T (n.2143+19A>T) c.925+19A>T (n.925+19A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324070T>C | CA2629370953 | HCN4 | c.2143+19A>G (n.2143+19A>G) c.925+19A>G (n.925+19A>G) | gnomAD v4 |
| 15 | g.73324070T>G | CA2629370954 | HCN4 | c.2143+19A>C (n.2143+19A>C) c.925+19A>C (n.925+19A>C) | gnomAD v4 |
| 15 | g.73324070T= | CA2187188961 | HCN4 | c.2143+19A= (n.2143+19A=) c.925+19A= (n.925+19A=) | |
| 15 | g.73324071G>A | CA272665372 | HCN4 | c.2143+18C>T (n.2143+18C>T) c.925+18C>T (n.925+18C>T) | dbSNP gnomAD v2 |
| 15 | g.73324071G= | CA2187188963 | HCN4 | c.2143+18C= (n.2143+18C=) c.925+18C= (n.925+18C=) | |
| 15 | g.73324072T>C | CA7649115 | HCN4 | c.2143+17A>G (n.2143+17A>G) c.925+17A>G (n.925+17A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324072T= | CA2187188966 | HCN4 | c.2143+17A= (n.2143+17A=) c.925+17A= (n.925+17A=) | |
| 15 | g.73324073G>A | CA619410600 | HCN4 | c.2143+16C>T (n.2143+16C>T) c.925+16C>T (n.925+16C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324073G>C | CA2629370955 | HCN4 | c.2143+16C>G (n.2143+16C>G) c.925+16C>G (n.925+16C>G) | gnomAD v4 |
| 15 | g.73324073G= | CA2187188969 | HCN4 | c.2143+16C= (n.2143+16C=) c.925+16C= (n.925+16C=) | |
| 15 | g.73324073G>T | CA2629370956 | HCN4 | c.2143+16C>A (n.2143+16C>A) c.925+16C>A (n.925+16C>A) | gnomAD v4 |
| 15 | g.73324074G>A | CA619410601 | HCN4 | c.2143+15C>T (n.2143+15C>T) c.925+15C>T (n.925+15C>T) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324074G= | CA2187188971 | HCN4 | c.2143+15C= (n.2143+15C=) c.925+15C= (n.925+15C=) | |
| 15 | g.73324074_73324075delinsGC | CA2187188972 | HCN4 | c.2143+14_2143+15delinsGC (n.2143+14_2143+15delinsGC) c.925+14_925+15delinsGC (n.925+14_925+15delinsGC) | |
| 15 | g.73324075C>A | CA2629370957 | HCN4 | c.2143+14G>T (n.2143+14G>T) c.925+14G>T (n.925+14G>T) | gnomAD v4 |
| 15 | g.73324078del | CA2187188974 | HCN4 | c.2143+14del (n.2143+14del) c.925+14del (n.925+14del) | ClinVar dbSNP |
| 15 | g.73324075_73324091del | CA2573151088 | HCN4 | c.2141_2143+14del c.923_925+14del | dbSNP |
| 15 | g.73324076C= | CA2187188976 | HCN4 | c.2143+13G= (n.2143+13G=) c.925+13G= (n.925+13G=) | |
| 15 | g.73324076C>T | CA7649116 | HCN4 | c.2143+13G>A (n.2143+13G>A) c.925+13G>A (n.925+13G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324077C>T | CA2572077763 | HCN4 | c.2143+12G>A (n.2143+12G>A) c.925+12G>A (n.925+12G>A) | gnomAD v4 |
| 15 | g.73324078C= | CA2187188979 | HCN4 | c.2143+11G= (n.2143+11G=) c.925+11G= (n.925+11G=) | |
| 15 | g.73324078C>G | CA619410602 | HCN4 | c.2143+11G>C (n.2143+11G>C) c.925+11G>C (n.925+11G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324079del | CA2697549182 | HCN4 | c.2143+10del (n.2143+10del) c.925+10del (n.925+10del) | ClinVar |
| 15 | g.73324079T>A | CA2187188983 | HCN4 | c.2143+10A>T (n.2143+10A>T) c.925+10A>T (n.925+10A>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324079T>C | CA715546980 | HCN4 | c.2143+10A>G (n.2143+10A>G) c.925+10A>G (n.925+10A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324079T= | CA2187188984 | HCN4 | c.2143+10A= (n.2143+10A=) c.925+10A= (n.925+10A=) | |
| 15 | g.73324080C>A | CA2629370958 | HCN4 | c.2143+9G>T (n.2143+9G>T) c.925+9G>T (n.925+9G>T) | gnomAD v4 |
| 15 | g.73324080C>T | CA2575783849 | HCN4 | c.2143+9G>A (n.2143+9G>A) c.925+9G>A (n.925+9G>A) | ClinVar gnomAD v4 |
| 15 | g.73324084dup | CA715546982 | HCN4 | c.2143+9dup (n.2143+9dup) c.925+9dup (n.925+9dup) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324081C= | CA2187188989 | HCN4 | c.2143+8G= (n.2143+8G=) c.925+8G= (n.925+8G=) | |
| 15 | g.73324081C>G | CA2575783850 | HCN4 | c.2143+8G>C (n.2143+8G>C) c.925+8G>C (n.925+8G>C) | |
| 15 | g.73324081C>T | CA1139664082 | HCN4 | c.2143+8G>A (n.2143+8G>A) c.925+8G>A (n.925+8G>A) | ClinVar dbSNP |
| 15 | g.73324082C>A | CA2629370959 | HCN4 | c.2143+7G>T (n.2143+7G>T) c.925+7G>T (n.925+7G>T) | gnomAD v4 |
| 15 | g.73324083C= | CA2187188992 | HCN4 | c.2143+6G= (n.2143+6G=) c.925+6G= (n.925+6G=) | |
| 15 | g.73324083C>G | CA619410603 | HCN4 | c.2143+6G>C (n.2143+6G>C) c.925+6G>C (n.925+6G>C) | dbSNP gnomAD v2 |
| 15 | g.73324083C>T | CA2629370960 | HCN4 | c.2143+6G>A (n.2143+6G>A) c.925+6G>A (n.925+6G>A) | gnomAD v4 |
| 15 | g.73324084C>A | CA7649117 | HCN4 | c.2143+5G>T (n.2143+5G>T) c.925+5G>T (n.925+5G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324084C= | CA2187188995 | HCN4 | c.2143+5G= (n.2143+5G=) c.925+5G= (n.925+5G=) | |
| 15 | g.73324084C>G | CA7649118 | HCN4 | c.2143+5G>C (n.2143+5G>C) c.925+5G>C (n.925+5G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324084C>T | CA7649119 | HCN4 | c.2143+5G>A (n.2143+5G>A) c.925+5G>A (n.925+5G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324085T>A | CA2187189004 | HCN4 | c.2143+4A>T (n.2143+4A>T) c.925+4A>T (n.925+4A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324085T>C | CA715547080 | HCN4 | c.2143+4A>G (n.2143+4A>G) c.925+4A>G (n.925+4A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324085T= | CA2187189002 | HCN4 | c.2143+4A= (n.2143+4A=) c.925+4A= (n.925+4A=) | |
| 15 | g.73324087A>C | CA393089773 | HCN4 | c.2143+2T>G (n.2143+2T>G) c.925+2T>G (n.925+2T>G) | gnomAD v3 gnomAD v4 |
| 15 | g.73324087A>G | CA393089776 | HCN4 | c.2143+2T>C (n.2143+2T>C) c.925+2T>C (n.925+2T>C) | |
| 15 | g.73324087A>T | CA393089779 | HCN4 | c.2143+2T>A (n.2143+2T>A) c.925+2T>A (n.925+2T>A) | |
| 15 | g.73324088C>A | CA393089782 | HCN4 | c.2143+1G>T (n.2143+1G>T) c.925+1G>T (n.925+1G>T) | |
| 15 | g.73324088C= | CA2187189010 | HCN4 | c.2143+1G= (n.2143+1G=) c.925+1G= (n.925+1G=) | |
| 15 | g.73324088C>G | CA393089786 | HCN4 | c.2143+1G>C (n.2143+1G>C) c.925+1G>C (n.925+1G>C) | ClinVar |
| 15 | g.73324088C>T | CA393089784 | HCN4 | c.2143+1G>A (n.2143+1G>A) c.925+1G>A (n.925+1G>A) | ClinVar dbSNP |
| 15 | g.73324089C>A | CA393089788 | HCN4 | c.2143G>T (p.Gly715Cys) c.925G>T (p.Gly309Cys) | |
| 15 | g.73324089C>G | CA393089791 | HCN4 | c.2143G>C (p.Gly715Arg) c.925G>C (p.Gly309Arg) | |
| 15 | g.73324089C>T | CA393089794 | HCN4 | c.2143G>A (p.Gly715Ser) c.925G>A (p.Gly309Ser) | |
| 15 | g.73324090A>C | CA393089798 | HCN4 | c.2142T>G (p.Ile714Met) c.924T>G (p.Ile308Met) | gnomAD v3 gnomAD v4 |
| 15 | g.73324090A>G | CA491478747 | HCN4 | c.2142T>C (p.Ile714=) c.924T>C (p.Ile308=) | |
| 15 | g.73324090A>T | CA491478749 | HCN4 | c.2142T>A (p.Ile714=) c.924T>A (p.Ile308=) | |
| 15 | g.73324091A>C | CA393089800 | HCN4 | c.2141T>G (p.Ile714Ser) c.923T>G (p.Ile308Ser) | |
| 15 | g.73324091A>G | CA393089803 | HCN4 | c.2141T>C (p.Ile714Thr) c.923T>C (p.Ile308Thr) | gnomAD v4 |
| 15 | g.73324091A>T | CA393089805 | HCN4 | c.2141T>A (p.Ile714Asn) c.923T>A (p.Ile308Asn) | |
| 15 | g.73324092T>A | CA393089808 | HCN4 | c.2140A>T (p.Ile714Phe) c.922A>T (p.Ile308Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324092T>C | CA393089810 | HCN4 | c.2140A>G (p.Ile714Val) c.922A>G (p.Ile308Val) | |
| 15 | g.73324092T>G | CA393089812 | HCN4 | c.2140A>C (p.Ile714Leu) c.922A>C (p.Ile308Leu) | |
| 15 | g.73324092T= | CA2187189014 | HCN4 | c.2140A= (p.Ile714=) c.922A= (p.Ile308=) | |
| 15 | g.73324092dup | CA2695220987 | HCN4 | c.2140dup (p.Ile714AsnfsTer27) c.922dup (p.Ile308AsnfsTer27) | |
| 15 | g.73324093G>A | CA491478754 | HCN4 | c.2139C>T (p.Arg713=) c.921C>T (p.Arg307=) | gnomAD v4 |
| 15 | g.73324093G>C | CA491478752 | HCN4 | c.2139C>G (p.Arg713=) c.921C>G (p.Arg307=) | |
| 15 | g.73324093G= | CA2187189017 | HCN4 | c.2139C= (p.Arg713=) c.921C= (p.Arg307=) | |
| 15 | g.73324093G>T | CA491478753 | HCN4 | c.2139C>A (p.Arg713=) c.921C>A (p.Arg307=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324102_73324110del | CA2629370961 | HCN4 | c.2131_2139del (p.Leu711_Arg713del) c.913_921del (p.Leu305_Arg307del) | ClinVar gnomAD v4 |
| 15 | g.73324094C>A | CA393089819 | HCN4 | c.2138G>T (p.Arg713Leu) c.920G>T (p.Arg307Leu) | gnomAD v4 |
| 15 | g.73324094C= | CA2187189019 | HCN4 | c.2138G= (p.Arg713=) c.920G= (p.Arg307=) | |
| 15 | g.73324094C>G | CA393089816 | HCN4 | c.2138G>C (p.Arg713Pro) c.920G>C (p.Arg307Pro) | |
| 15 | g.73324094C>T | CA7649120 | HCN4 | c.2138G>A (p.Arg713His) c.920G>A (p.Arg307His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73324095G>A | CA7649121 | HCN4 | c.2137C>T (p.Arg713Cys) c.919C>T (p.Arg307Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324095G>C | CA393089822 | HCN4 | c.2137C>G (p.Arg713Gly) c.919C>G (p.Arg307Gly) | |
| 15 | g.73324095G= | CA2187189024 | HCN4 | c.2137C= (p.Arg713=) c.919C= (p.Arg307=) | |
| 15 | g.73324095G>T | CA393089824 | HCN4 | c.2137C>A (p.Arg713Ser) c.919C>A (p.Arg307Ser) | |
| 15 | g.73324096G>A | CA491478758 | HCN4 | c.2136C>T (p.Asp712=) c.918C>T (p.Asp306=) | |
| 15 | g.73324096G>C | CA393089826 | HCN4 | c.2136C>G (p.Asp712Glu) c.918C>G (p.Asp306Glu) | |
| 15 | g.73324096G>T | CA393089828 | HCN4 | c.2136C>A (p.Asp712Glu) c.918C>A (p.Asp306Glu) | COSMIC |
| 15 | g.73324097T>A | CA393089835 | HCN4 | c.2135A>T (p.Asp712Val) c.917A>T (p.Asp306Val) | |
| 15 | g.73324097T>C | CA393089833 | HCN4 | c.2135A>G (p.Asp712Gly) c.917A>G (p.Asp306Gly) | |
| 15 | g.73324097T>G | CA393089831 | HCN4 | c.2135A>C (p.Asp712Ala) c.917A>C (p.Asp306Ala) | |
| 15 | g.73324098C>A | CA393089837 | HCN4 | c.2134G>T (p.Asp712Tyr) c.916G>T (p.Asp306Tyr) | |
| 15 | g.73324098C>G | CA393089838 | HCN4 | c.2134G>C (p.Asp712His) c.916G>C (p.Asp306His) | |
| 15 | g.73324098C>T | CA393089840 | HCN4 | c.2134G>A (p.Asp712Asn) c.916G>A (p.Asp306Asn) | |
| 15 | g.73324099C>A | CA491478765 | HCN4 | c.2133G>T (p.Leu711=) c.915G>T (p.Leu305=) | |
| 15 | g.73324099C= | CA2187189028 | HCN4 | c.2133G= (p.Leu711=) c.915G= (p.Leu305=) | |
| 15 | g.73324099C>G | CA491478766 | HCN4 | c.2133G>C (p.Leu711=) c.915G>C (p.Leu305=) | |
| 15 | g.73324099C>T | CA491478767 | HCN4 | c.2133G>A (p.Leu711=) c.915G>A (p.Leu305=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324100A= | CA2187189030 | HCN4 | c.2132T= (p.Leu711=) c.914T= (p.Leu305=) | |
| 15 | g.73324100A>C | CA393089843 | HCN4 | c.2132T>G (p.Leu711Arg) c.914T>G (p.Leu305Arg) | |
| 15 | g.73324100A>G | CA393089845 | HCN4 | c.2132T>C (p.Leu711Pro) c.914T>C (p.Leu305Pro) | dbSNP |
| 15 | g.73324100A>T | CA393089847 | HCN4 | c.2132T>A (p.Leu711Gln) c.914T>A (p.Leu305Gln) | |
| 15 | g.73324101G>A | CA7649122 | HCN4 | c.2131C>T (p.Leu711=) c.913C>T (p.Leu305=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324101G>C | CA393089850 | HCN4 | c.2131C>G (p.Leu711Val) c.913C>G (p.Leu305Val) | |
| 15 | g.73324101G= | CA2187189032 | HCN4 | c.2131C= (p.Leu711=) c.913C= (p.Leu305=) | |
| 15 | g.73324101G>T | CA393089849 | HCN4 | c.2131C>A (p.Leu711Met) c.913C>A (p.Leu305Met) | |
| 15 | g.73324102G>A | CA491478774 | HCN4 | c.2130C>T (p.Arg710=) c.912C>T (p.Arg304=) | gnomAD v4 |
| 15 | g.73324102G>C | CA491478775 | HCN4 | c.2130C>G (p.Arg710=) c.912C>G (p.Arg304=) | |
| 15 | g.73324102G>T | CA491478776 | HCN4 | c.2130C>A (p.Arg710=) c.912C>A (p.Arg304=) | gnomAD v4 |
| 15 | g.73324103C>A | CA393089852 | HCN4 | c.2129G>T (p.Arg710Leu) c.911G>T (p.Arg304Leu) | ClinVar gnomAD v4 |
| 15 | g.73324103C= | CA2187189034 | HCN4 | c.2129G= (p.Arg710=) c.911G= (p.Arg304=) | |
| 15 | g.73324103C>G | CA393089853 | HCN4 | c.2129G>C (p.Arg710Pro) c.911G>C (p.Arg304Pro) | |
| 15 | g.73324103C>T | CA272665427 | HCN4 | c.2129G>A (p.Arg710His) c.911G>A (p.Arg304His) | dbSNP gnomAD v4 |
| 15 | g.73324104G>A | CA393089856 | HCN4 | c.2128C>T (p.Arg710Cys) c.910C>T (p.Arg304Cys) | ClinVar gnomAD v4 |
| 15 | g.73324104G>C | CA7649123 | HCN4 | c.2128C>G (p.Arg710Gly) c.910C>G (p.Arg304Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324104G= | CA2187189036 | HCN4 | c.2128C= (p.Arg710=) c.910C= (p.Arg304=) | |
| 15 | g.73324104G>T | CA393089859 | HCN4 | c.2128C>A (p.Arg710Ser) c.910C>A (p.Arg304Ser) | |
| 15 | g.73324105G>A | CA491478803 | HCN4 | c.2127C>T (p.Asp709=) c.909C>T (p.Asp303=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73324105G>C | CA393089862 | HCN4 | c.2127C>G (p.Asp709Glu) c.909C>G (p.Asp303Glu) | |
| 15 | g.73324105G= | CA2187189038 | HCN4 | c.2127C= (p.Asp709=) c.909C= (p.Asp303=) | |
| 15 | g.73324105G>T | CA393089863 | HCN4 | c.2127C>A (p.Asp709Glu) c.909C>A (p.Asp303Glu) | |
| 15 | g.73324106T>A | CA393089866 | HCN4 | c.2126A>T (p.Asp709Val) c.908A>T (p.Asp303Val) | |
| 15 | g.73324106T>C | CA393089868 | HCN4 | c.2126A>G (p.Asp709Gly) c.908A>G (p.Asp303Gly) | |
| 15 | g.73324106T>G | CA393089869 | HCN4 | c.2126A>C (p.Asp709Ala) c.908A>C (p.Asp303Ala) | |
| 15 | g.73324107C>A | CA393089875 | HCN4 | c.2125G>T (p.Asp709Tyr) c.907G>T (p.Asp303Tyr) | |
| 15 | g.73324107C>G | CA393089873 | HCN4 | c.2125G>C (p.Asp709His) c.907G>C (p.Asp303His) | |
| 15 | g.73324107C>T | CA393089871 | HCN4 | c.2125G>A (p.Asp709Asn) c.907G>A (p.Asp303Asn) | |
| 15 | g.73324108C>A | CA491478809 | HCN4 | c.2124G>T (p.Leu708=) c.906G>T (p.Leu302=) | |
| 15 | g.73324108C>G | CA491478810 | HCN4 | c.2124G>C (p.Leu708=) c.906G>C (p.Leu302=) | |
| 15 | g.73324108C>T | CA491478811 | HCN4 | c.2124G>A (p.Leu708=) c.906G>A (p.Leu302=) | gnomAD v4 |
| 15 | g.73324109A>C | CA393089877 | HCN4 | c.2123T>G (p.Leu708Arg) c.905T>G (p.Leu302Arg) | |
| 15 | g.73324109A>G | CA393089879 | HCN4 | c.2123T>C (p.Leu708Pro) c.905T>C (p.Leu302Pro) | |
| 15 | g.73324109A>T | CA393089881 | HCN4 | c.2123T>A (p.Leu708Gln) c.905T>A (p.Leu302Gln) | |
| 15 | g.73324110G>A | CA491478817 | HCN4 | c.2122C>T (p.Leu708=) c.904C>T (p.Leu302=) | |
| 15 | g.73324110G>C | CA393089882 | HCN4 | c.2122C>G (p.Leu708Val) c.904C>G (p.Leu302Val) | |
| 15 | g.73324110G>T | CA393089884 | HCN4 | c.2122C>A (p.Leu708Met) c.904C>A (p.Leu302Met) | |
| 15 | g.73324111C>A | CA491478819 | HCN4 | c.2121G>T (p.Ala707=) c.903G>T (p.Ala301=) | dbSNP |
| 15 | g.73324111C= | CA2187189043 | HCN4 | c.2121G= (p.Ala707=) c.903G= (p.Ala301=) | |
| 15 | g.73324111C>G | CA491478820 | HCN4 | c.2121G>C (p.Ala707=) c.903G>C (p.Ala301=) | dbSNP |
| 15 | g.73324111C>T | CA491478821 | HCN4 | c.2121G>A (p.Ala707=) c.903G>A (p.Ala301=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324112G>A | CA393089887 | HCN4 | c.2120C>T (p.Ala707Val) c.902C>T (p.Ala301Val) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73324112G>C | CA393089889 | HCN4 | c.2120C>G (p.Ala707Gly) c.902C>G (p.Ala301Gly) | |
| 15 | g.73324112G>T | CA393089890 | HCN4 | c.2120C>A (p.Ala707Glu) c.902C>A (p.Ala301Glu) | |
| 15 | g.73324113C>A | CA393089893 | HCN4 | c.2119G>T (p.Ala707Ser) c.901G>T (p.Ala301Ser) | |
| 15 | g.73324113C>G | CA393089896 | HCN4 | c.2119G>C (p.Ala707Pro) c.901G>C (p.Ala301Pro) | |
| 15 | g.73324113C>T | CA393089894 | HCN4 | c.2119G>A (p.Ala707Thr) c.901G>A (p.Ala301Thr) | |
| 15 | g.73324114C>A | CA491478824 | HCN4 | c.2118G>T (p.Val706=) c.900G>T (p.Val300=) | |
| 15 | g.73324114C= | CA2187189048 | HCN4 | c.2118G= (p.Val706=) c.900G= (p.Val300=) | |
| 15 | g.73324114C>G | CA491478822 | HCN4 | c.2118G>C (p.Val706=) c.900G>C (p.Val300=) | |
| 15 | g.73324114C>T | CA7649124 | HCN4 | c.2118G>A (p.Val706=) c.900G>A (p.Val300=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324115A>C | CA393089900 | HCN4 | c.2117T>G (p.Val706Gly) c.899T>G (p.Val300Gly) | |
| 15 | g.73324115A>G | CA393089901 | HCN4 | c.2117T>C (p.Val706Ala) c.899T>C (p.Val300Ala) | |
| 15 | g.73324115A>T | CA393089902 | HCN4 | c.2117T>A (p.Val706Glu) c.899T>A (p.Val300Glu) | |
| 15 | g.73324116C>A | CA393089908 | HCN4 | c.2116G>T (p.Val706Leu) c.898G>T (p.Val300Leu) | gnomAD v4 |
| 15 | g.73324116C= | CA2187189051 | HCN4 | c.2116G= (p.Val706=) c.898G= (p.Val300=) | |
| 15 | g.73324116C>G | CA393089904 | HCN4 | c.2116G>C (p.Val706Leu) c.898G>C (p.Val300Leu) | |
| 15 | g.73324116C>T | CA393089906 | HCN4 | c.2116G>A (p.Val706Met) c.898G>A (p.Val300Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324117G>A | CA7649125 | HCN4 | c.2115C>T (p.Thr705=) c.897C>T (p.Thr299=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324117G>C | CA491478828 | HCN4 | c.2115C>G (p.Thr705=) c.897C>G (p.Thr299=) | ClinVar dbSNP COSMIC |
| 15 | g.73324117G= | CA2187189057 | HCN4 | c.2115C= (p.Thr705=) c.897C= (p.Thr299=) | |
| 15 | g.73324117G>T | CA491478830 | HCN4 | c.2115C>A (p.Thr705=) c.897C>A (p.Thr299=) | |
| 15 | g.73324118G>A | CA393089911 | HCN4 | c.2114C>T (p.Thr705Ile) c.896C>T (p.Thr299Ile) | |
| 15 | g.73324118G>C | CA393089913 | HCN4 | c.2114C>G (p.Thr705Ser) c.896C>G (p.Thr299Ser) | |
| 15 | g.73324118G>T | CA393089915 | HCN4 | c.2114C>A (p.Thr705Asn) c.896C>A (p.Thr299Asn) | |
| 15 | g.73324119T>A | CA393089917 | HCN4 | c.2113A>T (p.Thr705Ser) c.895A>T (p.Thr299Ser) | |
| 15 | g.73324119T>C | CA393089918 | HCN4 | c.2113A>G (p.Thr705Ala) c.895A>G (p.Thr299Ala) | gnomAD v3 gnomAD v4 |
| 15 | g.73324119T>G | CA393089921 | HCN4 | c.2113A>C (p.Thr705Pro) c.895A>C (p.Thr299Pro) | dbSNP |
| 15 | g.73324119T= | CA2187189061 | HCN4 | c.2113A= (p.Thr705=) c.895A= (p.Thr299=) | |
| 15 | g.73324120C>A | CA393089924 | HCN4 | c.2112G>T (p.Glu704Asp) c.894G>T (p.Glu298Asp) | |
| 15 | g.73324120C= | CA2187189064 | HCN4 | c.2112G= (p.Glu704=) c.894G= (p.Glu298=) | |
| 15 | g.73324120C>G | CA393089926 | HCN4 | c.2112G>C (p.Glu704Asp) c.894G>C (p.Glu298Asp) | |
| 15 | g.73324120C>T | CA7649126 | HCN4 | c.2112G>A (p.Glu704=) c.894G>A (p.Glu298=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324121T>A | CA393089929 | HCN4 | c.2111A>T (p.Glu704Val) c.893A>T (p.Glu298Val) | |
| 15 | g.73324121T>C | CA393089931 | HCN4 | c.2111A>G (p.Glu704Gly) c.893A>G (p.Glu298Gly) | |
| 15 | g.73324121T>G | CA393089933 | HCN4 | c.2111A>C (p.Glu704Ala) c.893A>C (p.Glu298Ala) | |
| 15 | g.73324122C>A | CA393089935 | HCN4 | c.2110G>T (p.Glu704Ter) c.892G>T (p.Glu298Ter) | |
| 15 | g.73324122C>G | CA393089939 | HCN4 | c.2110G>C (p.Glu704Gln) c.892G>C (p.Glu298Gln) | |
| 15 | g.73324122C>T | CA393089937 | HCN4 | c.2110G>A (p.Glu704Lys) c.892G>A (p.Glu298Lys) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73324123G>A | CA7649127 | HCN4 | c.2109C>T (p.Phe703=) c.891C>T (p.Phe297=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324123G>C | CA393089943 | HCN4 | c.2109C>G (p.Phe703Leu) c.891C>G (p.Phe297Leu) | |
| 15 | g.73324123G= | CA2187189069 | HCN4 | c.2109C= (p.Phe703=) c.891C= (p.Phe297=) | |
| 15 | g.73324123G>T | CA393089945 | HCN4 | c.2109C>A (p.Phe703Leu) c.891C>A (p.Phe297Leu) | |
| 15 | g.73324124A>C | CA393089947 | HCN4 | c.2108T>G (p.Phe703Cys) c.890T>G (p.Phe297Cys) | |
| 15 | g.73324124A>G | CA393089949 | HCN4 | c.2108T>C (p.Phe703Ser) c.890T>C (p.Phe297Ser) | |
| 15 | g.73324124A>T | CA393089950 | HCN4 | c.2108T>A (p.Phe703Tyr) c.890T>A (p.Phe297Tyr) | |
| 15 | g.73324125A>C | CA393089953 | HCN4 | c.2107T>G (p.Phe703Val) c.889T>G (p.Phe297Val) | |
| 15 | g.73324125A>G | CA393089956 | HCN4 | c.2107T>C (p.Phe703Leu) c.889T>C (p.Phe297Leu) | ClinVar |
| 15 | g.73324125A>T | CA393089958 | HCN4 | c.2107T>A (p.Phe703Ile) c.889T>A (p.Phe297Ile) | |
| 15 | g.73324126G>A | CA272665439 | HCN4 | c.2106C>T (p.Ala702=) c.888C>T (p.Ala296=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324126G>C | CA491478840 | HCN4 | c.2106C>G (p.Ala702=) c.888C>G (p.Ala296=) | |
| 15 | g.73324126G= | CA2187189075 | HCN4 | c.2106C= (p.Ala702=) c.888C= (p.Ala296=) | |
| 15 | g.73324126G>T | CA491478838 | HCN4 | c.2106C>A (p.Ala702=) c.888C>A (p.Ala296=) | |
| 15 | g.73324127G>A | CA393089962 | HCN4 | c.2105C>T (p.Ala702Val) c.887C>T (p.Ala296Val) | |
| 15 | g.73324127G>C | CA393089963 | HCN4 | c.2105C>G (p.Ala702Gly) c.887C>G (p.Ala296Gly) | |
| 15 | g.73324127G>T | CA393089964 | HCN4 | c.2105C>A (p.Ala702Asp) c.887C>A (p.Ala296Asp) | |
| 15 | g.73324128C>A | CA393089970 | HCN4 | c.2104G>T (p.Ala702Ser) c.886G>T (p.Ala296Ser) | |
| 15 | g.73324128C= | CA2187189077 | HCN4 | c.2104G= (p.Ala702=) c.886G= (p.Ala296=) | |
| 15 | g.73324128C>G | CA393089965 | HCN4 | c.2104G>C (p.Ala702Pro) c.886G>C (p.Ala296Pro) | |
| 15 | g.73324128C>T | CA393089967 | HCN4 | c.2104G>A (p.Ala702Thr) c.886G>A (p.Ala296Thr) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324129C>A | CA393089971 | HCN4 | c.2103G>T (p.Arg701Ser) c.885G>T (p.Arg295Ser) | |
| 15 | g.73324129C>G | CA393089973 | HCN4 | c.2103G>C (p.Arg701Ser) c.885G>C (p.Arg295Ser) | |
| 15 | g.73324129C>T | CA491478847 | HCN4 | c.2103G>A (p.Arg701=) c.885G>A (p.Arg295=) | |
| 15 | g.73324130C>A | CA393089975 | HCN4 | c.2102G>T (p.Arg701Met) c.884G>T (p.Arg295Met) | |
| 15 | g.73324130C>G | CA393089976 | HCN4 | c.2102G>C (p.Arg701Thr) c.884G>C (p.Arg295Thr) | |
| 15 | g.73324130C>T | CA393089978 | HCN4 | c.2102G>A (p.Arg701Lys) c.884G>A (p.Arg295Lys) |