Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23425781_23425783dup | CA011944 | MYH7 | c.2198_2200dup (p.Gly733_Gln734insArg) n.2304_2306dup | ClinVar dbSNP |
14 | g.23425783C>A | CA011936 | MYH7 | c.2198G>T (p.Gly733Val) n.2304G>T | ClinVar dbSNP |
14 | g.23425783C= | CA2123458503 | MYH7 | c.2198G= (p.Gly733=) n.2304G= | |
14 | g.23425783C>G | CA389048927 | MYH7 | c.2198G>C (p.Gly733Ala) n.2304G>C | |
14 | g.23425783C>T | CA011928 | MYH7 | c.2198G>A (p.Gly733Glu) n.2304G>A | ClinVar dbSNP |
14 | g.23425784C>A | CA389048930 | MYH7 | c.2197G>T (p.Gly733Ter) n.2303G>T | |
14 | g.23425784C>G | CA389048928 | MYH7 | c.2197G>C (p.Gly733Arg) n.2303G>C | gnomAD v4 |
14 | g.23425784C>T | CA389048929 | MYH7 | c.2197G>A (p.Gly733Arg) n.2303G>A | ClinVar gnomAD v4 |
14 | g.23425785C>A | CA389048931 | MYH7 | c.2196G>T (p.Glu732Asp) n.2302G>T | |
14 | g.23425785C= | CA2123458510 | MYH7 | c.2196G= (p.Glu732=) n.2302G= | |
14 | g.23425785C>G | CA389048932 | MYH7 | c.2196G>C (p.Glu732Asp) n.2302G>C | ClinVar dbSNP |
14 | g.23425785C>T | CA485766999 | MYH7 | c.2196G>A (p.Glu732=) n.2302G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.23425786T>A | CA389048933 | MYH7 | c.2195A>T (p.Glu732Val) n.2301A>T | |
14 | g.23425786T>C | CA389048934 | MYH7 | c.2195A>G (p.Glu732Gly) n.2301A>G | |
14 | g.23425786T>G | CA389048935 | MYH7 | c.2195A>C (p.Glu732Ala) n.2301A>C | |
14 | g.23425787C>A | CA389048936 | MYH7 | c.2194G>T (p.Glu732Ter) n.2300G>T | |
14 | g.23425787C= | CA2123458516 | MYH7 | c.2194G= (p.Glu732=) n.2300G= | |
14 | g.23425787C>G | CA389048937 | MYH7 | c.2194G>C (p.Glu732Gln) n.2300G>C | |
14 | g.23425787C>T | CA389048938 | MYH7 | c.2194G>A (p.Glu732Lys) n.2300G>A | dbSNP gnomAD v2 |
14 | g.23425788A= | CA2123458520 | MYH7 | c.2193T= (p.Pro731=) n.2299T= | |
14 | g.23425788A>C | CA485767000 | MYH7 | c.2193T>G (p.Pro731=) n.2299T>G | |
14 | g.23425788A>G | CA485767002 | MYH7 | c.2193T>C (p.Pro731=) n.2299T>C | dbSNP |
14 | g.23425788A>T | CA485767003 | MYH7 | c.2193T>A (p.Pro731=) n.2299T>A | gnomAD v4 |
14 | g.23425789G>A | CA389048939 | MYH7 | c.2192C>T (p.Pro731Leu) n.2298C>T | ClinVar dbSNP COSMIC |
14 | g.23425789G>C | CA389048940 | MYH7 | c.2192C>G (p.Pro731Arg) n.2298C>G | ClinVar dbSNP |
14 | g.23425789G= | CA2123458529 | MYH7 | c.2192C= (p.Pro731=) n.2298C= | |
14 | g.23425789G>T | CA389048941 | MYH7 | c.2192C>A (p.Pro731His) n.2298C>A | |
14 | g.23425790G>A | CA011922 | MYH7 | c.2191C>T (p.Pro731Ser) n.2297C>T | ClinVar dbSNP COSMIC |
14 | g.23425790G>C | CA011914 | MYH7 | c.2191C>G (p.Pro731Ala) n.2297C>G | ClinVar dbSNP |
14 | g.23425790G= | CA2123458539 | MYH7 | c.2191C= (p.Pro731=) n.2297C= | |
14 | g.23425790G>T | CA16603250 | MYH7 | c.2191C>A (p.Pro731Thr) n.2297C>A | ClinVar dbSNP |
14 | g.23425791G>A | CA485767005 | MYH7 | c.2190C>T (p.Ile730=) n.2296C>T | |
14 | g.23425791G>C | CA389048942 | MYH7 | c.2190C>G (p.Ile730Met) n.2296C>G | |
14 | g.23425791G>T | CA485767007 | MYH7 | c.2190C>A (p.Ile730=) n.2296C>A | |
14 | g.23425792A= | CA2123458550 | MYH7 | c.2189T= (p.Ile730=) n.2295T= | |
14 | g.23425792A>C | CA389048943 | MYH7 | c.2189T>G (p.Ile730Ser) n.2295T>G | |
14 | g.23425792A>G | CA16614089 | MYH7 | c.2189T>C (p.Ile730Thr) n.2295T>C | ClinVar dbSNP |
14 | g.23425792A>T | CA389048944 | MYH7 | c.2189T>A (p.Ile730Asn) n.2295T>A | ClinVar dbSNP |
14 | g.23425793T>A | CA389048945 | MYH7 | c.2188A>T (p.Ile730Phe) n.2294A>T | |
14 | g.23425793T>C | CA389048946 | MYH7 | c.2188A>G (p.Ile730Val) n.2294A>G | |
14 | g.23425793T>G | CA389048947 | MYH7 | c.2188A>C (p.Ile730Leu) n.2294A>C | |
14 | g.23425794G>A | CA485767012 | MYH7 | c.2187C>T (p.Ala729=) n.2293C>T | |
14 | g.23425794G>C | CA485767010 | MYH7 | c.2187C>G (p.Ala729=) n.2293C>G | |
14 | g.23425794G= | CA2123458585 | MYH7 | c.2187C= (p.Ala729=) n.2293C= | |
14 | g.23425794G>T | CA011910 | MYH7 | c.2187C>A (p.Ala729=) n.2293C>A | ClinVar dbSNP |
14 | g.23425795G>A | CA389048948 | MYH7 | c.2186C>T (p.Ala729Val) n.2292C>T | gnomAD v4 |
14 | g.23425795G>C | CA389048949 | MYH7 | c.2186C>G (p.Ala729Gly) n.2292C>G | |
14 | g.23425795G>T | CA389048950 | MYH7 | c.2186C>A (p.Ala729Asp) n.2292C>A | |
14 | g.23425796C>A | CA389048951 | MYH7 | c.2185G>T (p.Ala729Ser) n.2291G>T | |
14 | g.23425796C>G | CA389048952 | MYH7 | c.2185G>C (p.Ala729Pro) n.2291G>C |