| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23431650C>A | CA389052295 | MYH7 | c.667G>T (p.Ala223Ser) n.773G>T | |
| 14 | g.23431650C= | CA2123452233 | MYH7 | c.667G= (p.Ala223=) n.773G= | |
| 14 | g.23431650C>G | CA389052296 | MYH7 | c.667G>C (p.Ala223Pro) n.773G>C | |
| 14 | g.23431650C>T | CA016610 | MYH7 | c.667G>A (p.Ala223Thr) n.773G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23431651C>A | CA389052297 | MYH7 | c.666G>T (p.Gln222His) n.772G>T | |
| 14 | g.23431651C= | CA2123452238 | MYH7 | c.666G= (p.Gln222=) n.772G= | |
| 14 | g.23431651C>G | CA389052298 | MYH7 | c.666G>C (p.Gln222His) n.772G>C | ClinVar dbSNP |
| 14 | g.23431651C>T | CA485767359 | MYH7 | c.666G>A (p.Gln222=) n.772G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23431652T>A | CA389052299 | MYH7 | c.665A>T (p.Gln222Leu) n.771A>T | |
| 14 | g.23431652T>C | CA389052300 | MYH7 | c.665A>G (p.Gln222Arg) n.771A>G | |
| 14 | g.23431652T>G | CA389052301 | MYH7 | c.665A>C (p.Gln222Pro) n.771A>C | |
| 14 | g.23431653G>A | CA389052303 | MYH7 | c.664C>T (p.Gln222Ter) n.770C>T | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23431653G>C | CA389052302 | MYH7 | c.664C>G (p.Gln222Glu) n.770C>G | |
| 14 | g.23431653G= | CA2123452243 | MYH7 | c.664C= (p.Gln222=) n.770C= | |
| 14 | g.23431653G>T | CA16614501 | MYH7 | c.664C>A (p.Gln222Lys) n.770C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23431654G>A | CA485767360 | MYH7 | c.663C>T (p.Ile221=) n.769C>T | |
| 14 | g.23431654G>C | CA389052304 | MYH7 | c.663C>G (p.Ile221Met) n.769C>G | |
| 14 | g.23431654G>T | CA485767361 | MYH7 | c.663C>A (p.Ile221=) n.769C>A | |
| 14 | g.23431655A= | CA2123452249 | MYH7 | c.662T= (p.Ile221=) n.768T= | |
| 14 | g.23431655A>C | CA389052305 | MYH7 | c.662T>G (p.Ile221Ser) n.768T>G | |
| 14 | g.23431655A>G | CA10583173 | MYH7 | c.662T>C (p.Ile221Thr) n.768T>C | ClinVar dbSNP |
| 14 | g.23431655A>T | CA389052306 | MYH7 | c.662T>A (p.Ile221Asn) n.768T>A | |
| 14 | g.23431656T>A | CA389052307 | MYH7 | c.661A>T (p.Ile221Phe) n.767A>T | |
| 14 | g.23431656T>C | CA389052308 | MYH7 | c.661A>G (p.Ile221Val) n.767A>G | |
| 14 | g.23431656T>G | CA389052309 | MYH7 | c.661A>C (p.Ile221Leu) n.767A>C | |
| 14 | g.23431657G>A | CA485767362 | MYH7 | c.660C>T (p.Ile220=) n.766C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23431657G>C | CA389052310 | MYH7 | c.660C>G (p.Ile220Met) n.766C>G | |
| 14 | g.23431657G= | CA2123452254 | MYH7 | c.660C= (p.Ile220=) n.766C= | |
| 14 | g.23431657G>T | CA485767363 | MYH7 | c.660C>A (p.Ile220=) n.766C>A | dbSNP |
| 14 | g.23431658A>C | CA389052311 | MYH7 | c.659T>G (p.Ile220Ser) n.765T>G | |
| 14 | g.23431658A>G | CA389052312 | MYH7 | c.659T>C (p.Ile220Thr) n.765T>C | |
| 14 | g.23431658A>T | CA389052313 | MYH7 | c.659T>A (p.Ile220Asn) n.765T>A | |
| 14 | g.23431659T>A | CA389052314 | MYH7 | c.658A>T (p.Ile220Phe) n.764A>T | |
| 14 | g.23431659T>C | CA048726 | MYH7 | c.658A>G (p.Ile220Val) n.764A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23431659T>G | CA10644000 | MYH7 | c.658A>C (p.Ile220Leu) n.764A>C | ClinVar dbSNP |
| 14 | g.23431659T= | CA2123452261 | MYH7 | c.658A= (p.Ile220=) n.764A= | |
| 14 | g.23431660C>A | CA389052316 | MYH7 | c.657G>T (p.Gln219His) n.763G>T | |
| 14 | g.23431660C>G | CA389052315 | MYH7 | c.657G>C (p.Gln219His) n.763G>C | |
| 14 | g.23431660C>T | CA485767364 | MYH7 | c.657G>A (p.Gln219=) n.763G>A | gnomAD v4 |
| 14 | g.23431661T>A | CA389052317 | MYH7 | c.656A>T (p.Gln219Leu) n.762A>T | |
| 14 | g.23431661T>C | CA389052318 | MYH7 | c.656A>G (p.Gln219Arg) n.762A>G | |
| 14 | g.23431661T>G | CA389052319 | MYH7 | c.656A>C (p.Gln219Pro) n.762A>C | |
| 14 | g.23431662G>A | CA389052320 | MYH7 | c.655C>T (p.Gln219Ter) n.761C>T | |
| 14 | g.23431662G>C | CA389052321 | MYH7 | c.655C>G (p.Gln219Glu) n.761C>G | ClinVar dbSNP |
| 14 | g.23431662G= | CA2123452273 | MYH7 | c.655C= (p.Gln219=) n.761C= | |
| 14 | g.23431662G>T | CA389052322 | MYH7 | c.655C>A (p.Gln219Lys) n.761C>A | COSMIC |
| 14 | g.23431663G>A | CA485767365 | MYH7 | c.654C>T (p.Asp218=) n.760C>T | |
| 14 | g.23431663G>C | CA389052324 | MYH7 | c.654C>G (p.Asp218Glu) n.760C>G | |
| 14 | g.23431663G>T | CA389052323 | MYH7 | c.654C>A (p.Asp218Glu) n.760C>A | |
| 14 | g.23431664T>A | CA389052325 | MYH7 | c.653A>T (p.Asp218Val) n.759A>T |