Duplication | NM_000256.3(MYBPC3):c.2258dup (p.Lys754fs) | MYBPC3 | Pathogenic | 11 | 47360120 | 47360121 | C | CA | criteria provided, multiple submitters, no conflicts | ClinGen:CA5975367 |
single nucleotide variant | NM_000256.3(MYBPC3):c.1927G>T (p.Glu643Ter) | MYBPC3 | Pathogenic | 11 | 47362554 | 47362554 | C | A | criteria provided, single submitter | ClinGen:CA380323208 |
Indel | NM_000256.3(MYBPC3):c.1827_1846delinsTACAGC (p.Asp610fs) | MYBPC3 | Pathogenic | 11 | 47362740 | 47362759 | AGCTGTAGTCAGCCTCGTCG | GCTGTA | criteria provided, single submitter | ClinGen:CA658797629 |
Deletion | NM_000256.3(MYBPC3):c.1570_1594del (p.His524fs) | MYBPC3 | Pathogenic | 11 | 47364159 | 47364183 | CCCCCGCTAGTGCACAGTGCATAGTG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658797633 |
Deletion | NM_000256.3(MYBPC3):c.1483del (p.Arg495fs) | MYBPC3 | Pathogenic | 11 | 47364270 | 47364270 | CG | C | criteria provided, single submitter | ClinGen:CA658797635 |
Duplication | NM_000256.3(MYBPC3):c.1103_1107dup (p.Glu370fs) | MYBPC3 | Pathogenic | 11 | 47365158 | 47365159 | C | CCAGCT | criteria provided, multiple submitters, no conflicts | ClinGen:CA658797638 |
single nucleotide variant | NM_000256.3(MYBPC3):c.660T>G (p.Tyr220Ter) | MYBPC3 | Pathogenic | 11 | 47370087 | 47370087 | A | C | criteria provided, single submitter | ClinGen:CA380336488 |
Deletion | NM_000256.3(MYBPC3):c.505_505+7del | MYBPC3 | Pathogenic | 11 | 47371558 | 47371565 | ACACTCACC | A | criteria provided, single submitter | ClinGen:CA658797645 |
Deletion | NM_000256.3(MYBPC3):c.480del (p.Pro161fs) | MYBPC3 | Pathogenic | 11 | 47371590 | 47371590 | GC | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA658797646 |
Duplication | NM_000256.3(MYBPC3):c.405dup (p.Gly136fs) | MYBPC3 | Pathogenic | 11 | 47372053 | 47372054 | C | CT | criteria provided, single submitter | ClinGen:CA658797647 |