Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23417586C>A | CA389040281 | MHRT,MYH7 | c.4270G>T (p.Glu1424Ter) n.867C>A | |
14 | g.23417586C= | CA2123469604 | MHRT,MYH7 | c.4270G= (p.Glu1424=) n.867C= | |
14 | g.23417586C>G | CA389040283 | MHRT,MYH7 | c.4270G>C (p.Glu1424Gln) n.867C>G | |
14 | g.23417586C>T | CA014734 | MHRT,MYH7 | c.4270G>A (p.Glu1424Lys) n.867C>T | ClinVar dbSNP COSMIC |
14 | g.23417587A= | CA2123469610 | MHRT,MYH7 | c.4269T= (p.Asn1423=) n.868A= | |
14 | g.23417587A>C | CA389040285 | MHRT,MYH7 | c.4269T>G (p.Asn1423Lys) n.868A>C | dbSNP gnomAD v4 |
14 | g.23417587A>G | CA485617819 | MHRT,MYH7 | c.4269T>C (p.Asn1423=) n.868A>G | dbSNP |
14 | g.23417587A>T | CA389040286 | MHRT,MYH7 | c.4269T>A (p.Asn1423Lys) n.868A>T | |
14 | g.23417588T>A | CA389040288 | MHRT,MYH7 | c.4268A>T (p.Asn1423Ile) n.869T>A | |
14 | g.23417588T>C | CA389040290 | MHRT,MYH7 | c.4268A>G (p.Asn1423Ser) n.869T>C | |
14 | g.23417588T>G | CA389040291 | MHRT,MYH7 | c.4268A>C (p.Asn1423Thr) n.869T>G | |
14 | g.23417589T>A | CA389040293 | MHRT,MYH7 | c.4267A>T (p.Asn1423Tyr) n.870T>A | |
14 | g.23417589T>C | CA389040294 | MHRT,MYH7 | c.4267A>G (p.Asn1423Asp) n.870T>C | |
14 | g.23417589T>G | CA389040296 | MHRT,MYH7 | c.4267A>C (p.Asn1423His) n.870T>G | |
14 | g.23417590C>A | CA389040297 | MHRT,MYH7 | c.4266G>T (p.Gln1422His) n.871C>A | |
14 | g.23417590C>G | CA389040299 | MHRT,MYH7 | c.4266G>C (p.Gln1422His) n.871C>G | |
14 | g.23417590C>T | CA485617820 | MHRT,MYH7 | c.4266G>A (p.Gln1422=) n.871C>T | |
14 | g.23417591T>A | CA389040300 | MHRT,MYH7 | c.4265A>T (p.Gln1422Leu) n.872T>A | |
14 | g.23417591T>C | CA389040302 | MHRT,MYH7 | c.4265A>G (p.Gln1422Arg) n.872T>C | |
14 | g.23417591T>G | CA389040304 | MHRT,MYH7 | c.4265A>C (p.Gln1422Pro) n.872T>G | |
14 | g.23417592G>A | CA389040306 | MHRT,MYH7 | c.4264C>T (p.Gln1422Ter) n.873G>A | |
14 | g.23417592G>C | CA389040308 | MHRT,MYH7 | c.4264C>G (p.Gln1422Glu) n.873G>C | |
14 | g.23417592G>T | CA389040307 | MHRT,MYH7 | c.4264C>A (p.Gln1422Lys) n.873G>T | ClinVar |
14 | g.23417593T>A | CA485617821 | MHRT,MYH7 | c.4263A>T (p.Leu1421=) n.874T>A | |
14 | g.23417593T>C | CA485617822 | MHRT,MYH7 | c.4263A>G (p.Leu1421=) n.874T>C | dbSNP |
14 | g.23417593T>G | CA485617823 | MHRT,MYH7 | c.4263A>C (p.Leu1421=) n.874T>G | |
14 | g.23417593T= | CA2123469616 | MHRT,MYH7 | c.4263A= (p.Leu1421=) n.874T= | |
14 | g.23417594A>C | CA389040310 | MHRT,MYH7 | c.4262T>G (p.Leu1421Arg) n.875A>C | |
14 | g.23417594A>G | CA389040314 | MHRT,MYH7 | c.4262T>C (p.Leu1421Pro) n.875A>G | |
14 | g.23417594A>T | CA389040312 | MHRT,MYH7 | c.4262T>A (p.Leu1421Gln) n.875A>T | |
14 | g.23417595G>A | CA485617824 | MHRT,MYH7 | c.4261C>T (p.Leu1421=) n.876G>A | |
14 | g.23417595G>C | CA389040315 | MHRT,MYH7 | c.4261C>G (p.Leu1421Val) n.876G>C | |
14 | g.23417595G= | CA2123469625 | MHRT,MYH7 | c.4261C= (p.Leu1421=) n.876G= | |
14 | g.23417595G>T | CA389040317 | MHRT,MYH7 | c.4261C>A (p.Leu1421Ile) n.876G>T | gnomAD v4 |
14 | g.23417596C>A | CA485617831 | MYH7 | c.4260G>T (p.Arg1420=) | |
14 | g.23417596C>G | CA485617829 | MYH7 | c.4260G>C (p.Arg1420=) | dbSNP |
14 | g.23417596C>T | CA485617830 | MYH7 | c.4260G>A (p.Arg1420=) | |
14 | g.23417597C>A | CA389040319 | MYH7 | c.4259G>T (p.Arg1420Leu) | COSMIC |
14 | g.23417597C= | CA2123441084 | MYH7 | c.4259G= (p.Arg1420=) | |
14 | g.23417597C>G | CA389040321 | MYH7 | c.4259G>C (p.Arg1420Pro) | ClinVar dbSNP |
14 | g.23417597C>T | CA014728 | MYH7 | c.4259G>A (p.Arg1420Gln) | ClinVar dbSNP gnomAD v4 COSMIC |
14 | g.23417598G>A | CA014718 | MYH7 | c.4258C>T (p.Arg1420Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23417598G>C | CA389040324 | MYH7 | c.4258C>G (p.Arg1420Gly) | |
14 | g.23417598G= | CA2123441092 | MYH7 | c.4258C= (p.Arg1420=) | |
14 | g.23417598G>T | CA485617833 | MYH7 | c.4258C>A (p.Arg1420=) | ClinVar dbSNP gnomAD v4 |
14 | g.23417599G>A | CA485617834 | MYH7 | c.4257C>T (p.His1419=) | ClinVar dbSNP |
14 | g.23417599G>C | CA389040326 | MYH7 | c.4257C>G (p.His1419Gln) | |
14 | g.23417599G= | CA2123441098 | MYH7 | c.4257C= (p.His1419=) | |
14 | g.23417599G>T | CA389040327 | MYH7 | c.4257C>A (p.His1419Gln) | gnomAD v4 |
14 | g.23417600T>A | CA389040328 | MYH7 | c.4256A>T (p.His1419Leu) | ClinVar |