| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73367625G>A | CA272700035 | HCN4 | c.646C>T (p.Arg216Cys) | dbSNP |
| 15 | g.73367625G>C | CA393097365 | HCN4 | c.646C>G (p.Arg216Gly) | ClinVar dbSNP |
| 15 | g.73367625G= | CA2187194472 | HCN4 | c.646C= (p.Arg216=) | |
| 15 | g.73367625G>T | CA393097366 | HCN4 | c.646C>A (p.Arg216Ser) | |
| 15 | g.73367626C>A | CA393097367 | HCN4 | c.645G>T (p.Gln215His) | |
| 15 | g.73367626C>G | CA393097368 | HCN4 | c.645G>C (p.Gln215His) | |
| 15 | g.73367626C>T | CA491479497 | HCN4 | c.645G>A (p.Gln215=) | |
| 15 | g.73367627T>A | CA393097371 | HCN4 | c.644A>T (p.Gln215Leu) | |
| 15 | g.73367627T>C | CA393097373 | HCN4 | c.644A>G (p.Gln215Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73367627T>G | CA393097374 | HCN4 | c.644A>C (p.Gln215Pro) | |
| 15 | g.73367628G>A | CA272700039 | HCN4 | c.643C>T (p.Gln215Ter) | dbSNP |
| 15 | g.73367628G>C | CA393097375 | HCN4 | c.643C>G (p.Gln215Glu) | |
| 15 | g.73367628G= | CA2187194473 | HCN4 | c.643C= (p.Gln215=) | |
| 15 | g.73367628G>T | CA393097377 | HCN4 | c.643C>A (p.Gln215Lys) | |
| 15 | g.73367629C>A | CA7649444 | HCN4 | c.642G>T (p.Met214Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367629C= | CA2187194474 | HCN4 | c.642G= (p.Met214=) | |
| 15 | g.73367629C>G | CA393097382 | HCN4 | c.642G>C (p.Met214Ile) | |
| 15 | g.73367629C>T | CA393097383 | HCN4 | c.642G>A (p.Met214Ile) | |
| 15 | g.73367630A>C | CA393097385 | HCN4 | c.641T>G (p.Met214Arg) | |
| 15 | g.73367630A>G | CA393097386 | HCN4 | c.641T>C (p.Met214Thr) | |
| 15 | g.73367630A>T | CA393097388 | HCN4 | c.641T>A (p.Met214Lys) | |
| 15 | g.73367631T>A | CA7649445 | HCN4 | c.640A>T (p.Met214Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367631T>C | CA393097390 | HCN4 | c.640A>G (p.Met214Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367631T>G | CA393097391 | HCN4 | c.640A>C (p.Met214Leu) | |
| 15 | g.73367631T= | CA2187194475 | HCN4 | c.640A= (p.Met214=) | |
| 15 | g.73367632G>A | CA491479498 | HCN4 | c.639C>T (p.Phe213=) | ClinVar dbSNP COSMIC |
| 15 | g.73367632G>C | CA393097392 | HCN4 | c.639C>G (p.Phe213Leu) | |
| 15 | g.73367632G= | CA2187194476 | HCN4 | c.639C= (p.Phe213=) | |
| 15 | g.73367632G>T | CA393097393 | HCN4 | c.639C>A (p.Phe213Leu) | |
| 15 | g.73367633A>C | CA393097396 | HCN4 | c.638T>G (p.Phe213Cys) | |
| 15 | g.73367633A>G | CA393097398 | HCN4 | c.638T>C (p.Phe213Ser) | |
| 15 | g.73367633A>T | CA393097395 | HCN4 | c.638T>A (p.Phe213Tyr) | |
| 15 | g.73367634A>C | CA393097399 | HCN4 | c.637T>G (p.Phe213Val) | |
| 15 | g.73367634A>G | CA393097401 | HCN4 | c.637T>C (p.Phe213Leu) | gnomAD v4 |
| 15 | g.73367634A>T | CA393097402 | HCN4 | c.637T>A (p.Phe213Ile) | |
| 15 | g.73367634_73367635insTTTTTTAAT | CA2629389807 | HCN4 | c.636_637insATTAAAAAA (p.Gly212_Phe213insIleLysLys) | gnomAD v4 |
| 15 | g.73367635G>A | CA491479499 | HCN4 | c.636C>T (p.Gly212=) | ClinVar gnomAD v4 |
| 15 | g.73367635G>C | CA491479500 | HCN4 | c.636C>G (p.Gly212=) | ClinVar gnomAD v4 |
| 15 | g.73367635G>T | CA491479501 | HCN4 | c.636C>A (p.Gly212=) | |
| 15 | g.73367636C>A | CA393097403 | HCN4 | c.635G>T (p.Gly212Val) | |
| 15 | g.73367636C= | CA2187194477 | HCN4 | c.635G= (p.Gly212=) | |
| 15 | g.73367636C>G | CA393097405 | HCN4 | c.635G>C (p.Gly212Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367636C>T | CA393097407 | HCN4 | c.635G>A (p.Gly212Asp) | |
| 15 | g.73367637C>A | CA393097409 | HCN4 | c.634G>T (p.Gly212Cys) | |
| 15 | g.73367637C>G | CA393097410 | HCN4 | c.634G>C (p.Gly212Arg) | |
| 15 | g.73367637C>T | CA393097412 | HCN4 | c.634G>A (p.Gly212Ser) | |
| 15 | g.73367638G>A | CA7649446 | HCN4 | c.633C>T (p.Ala211=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367638G>C | CA491479502 | HCN4 | c.633C>G (p.Ala211=) | ClinVar dbSNP |
| 15 | g.73367638G= | CA2187194478 | HCN4 | c.633C= (p.Ala211=) | |
| 15 | g.73367638G>T | CA7649447 | HCN4 | c.633C>A (p.Ala211=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |