Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.46859509C>A | CA013830 | MYL3 | c.447G>T (p.Met149Ile) n.669G>T n.405G>T | ClinVar dbSNP COSMIC |
3 | g.46859509C= | CA1362297093 | MYL3 | c.447G= (p.Met149=) n.669G= n.405G= | |
3 | g.46859509C>G | CA352495936 | MYL3 | c.447G>C (p.Met149Ile) n.669G>C n.405G>C | |
3 | g.46859509C>T | CA013812 | MYL3 | c.447G>A (p.Met149Ile) n.669G>A n.405G>A | ClinVar dbSNP |
3 | g.46859510A= | CA1362297094 | MYL3 | c.446T= (p.Met149=) n.668T= n.404T= | |
3 | g.46859510A>C | CA352495939 | MYL3 | c.446T>G (p.Met149Arg) n.668T>G n.404T>G | |
3 | g.46859510A>G | CA013800 | MYL3 | c.446T>C (p.Met149Thr) n.668T>C n.404T>C | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
3 | g.46859510A>T | CA352495937 | MYL3 | c.446T>A (p.Met149Lys) n.668T>A n.404T>A | |
3 | g.46859511T>A | CA352495941 | MYL3 | c.445A>T (p.Met149Leu) n.667A>T n.403A>T | |
3 | g.46859511T>C | CA013784 | MYL3 | c.445A>G (p.Met149Val) n.667A>G n.403A>G | ClinVar dbSNP |
3 | g.46859511T>G | CA352495942 | MYL3 | c.445A>C (p.Met149Leu) n.667A>C n.403A>C | |
3 | g.46859511T= | CA1362297095 | MYL3 | c.445A= (p.Met149=) n.667A= n.403A= | |
3 | g.46859512G>A | CA433474375 | MYL3 | c.444C>T (p.Val148=) n.666C>T n.402C>T | dbSNP |
3 | g.46859512G>C | CA433474376 | MYL3 | c.444C>G (p.Val148=) n.666C>G n.402C>G | dbSNP gnomAD v3 gnomAD v4 |
3 | g.46859512G= | CA1362297096 | MYL3 | c.444C= (p.Val148=) n.666C= n.402C= | |
3 | g.46859512G>T | CA433474377 | MYL3 | c.444C>A (p.Val148=) n.666C>A n.402C>A | |
3 | g.46859513A>C | CA352495943 | MYL3 | c.443T>G (p.Val148Gly) n.665T>G n.401T>G | |
3 | g.46859513A>G | CA352495944 | MYL3 | c.443T>C (p.Val148Ala) n.665T>C n.401T>C | |
3 | g.46859513A>T | CA352495947 | MYL3 | c.443T>A (p.Val148Asp) n.665T>A n.401T>A | |
3 | g.46859514C>A | CA352495950 | MYL3 | c.442G>T (p.Val148Phe) n.664G>T n.400G>T | |
3 | g.46859514C>G | CA352495953 | MYL3 | c.442G>C (p.Val148Leu) n.664G>C n.400G>C | |
3 | g.46859514C>T | CA352495956 | MYL3 | c.442G>A (p.Val148Ile) n.664G>A n.400G>A | |
3 | g.46859515A>C | CA433474378 | MYL3 | c.441T>G (p.Thr147=) n.663T>G n.399T>G | |
3 | g.46859515A>G | CA433474379 | MYL3 | c.441T>C (p.Thr147=) n.663T>C n.399T>C | ClinVar gnomAD v4 |
3 | g.46859515A>T | CA433474380 | MYL3 | c.441T>A (p.Thr147=) n.663T>A n.399T>A | dbSNP |
3 | g.46859516G>A | CA352495959 | MYL3 | c.440C>T (p.Thr147Ile) n.662C>T n.398C>T | |
3 | g.46859516G>C | CA352495962 | MYL3 | c.440C>G (p.Thr147Ser) n.662C>G n.398C>G | |
3 | g.46859516G>T | CA352495965 | MYL3 | c.440C>A (p.Thr147Asn) n.662C>A n.398C>A | |
3 | g.46859517T>A | CA352495971 | MYL3 | c.439A>T (p.Thr147Ser) n.661A>T n.397A>T | |
3 | g.46859517T>C | CA044165 | MYL3 | c.439A>G (p.Thr147Ala) n.661A>G n.397A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.46859517T>G | CA352495967 | MYL3 | c.439A>C (p.Thr147Pro) n.661A>C n.397A>C | |
3 | g.46859517T= | CA1362297097 | MYL3 | c.439A= (p.Thr147=) n.661A= n.397A= | |
3 | g.46859518G>A | CA433474381 | MYL3 | c.438C>T (p.Gly146=) n.660C>T n.396C>T | |
3 | g.46859518G>C | CA433474382 | MYL3 | c.438C>G (p.Gly146=) n.660C>G n.396C>G | |
3 | g.46859518G= | CA1362297098 | MYL3 | c.438C= (p.Gly146=) n.660C= n.396C= | |
3 | g.46859518G>T | CA433474383 | MYL3 | c.438C>A (p.Gly146=) n.660C>A n.396C>A | dbSNP |
3 | g.46859519C>A | CA352495974 | MYL3 | c.437G>T (p.Gly146Val) n.659G>T n.395G>T | |
3 | g.46859519C= | CA1362297099 | MYL3 | c.437G= (p.Gly146=) n.659G= n.395G= | |
3 | g.46859519C>G | CA352495977 | MYL3 | c.437G>C (p.Gly146Ala) n.659G>C n.395G>C | |
3 | g.46859519C>T | CA352495979 | MYL3 | c.437G>A (p.Gly146Asp) n.659G>A n.395G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
3 | g.46859520C>A | CA352495981 | MYL3 | c.436G>T (p.Gly146Cys) n.658G>T n.394G>T | |
3 | g.46859520C>G | CA352495984 | MYL3 | c.436G>C (p.Gly146Arg) n.658G>C n.394G>C | |
3 | g.46859520C>T | CA352495986 | MYL3 | c.436G>A (p.Gly146Ser) n.658G>A n.394G>A | |
3 | g.46859521A= | CA1362297100 | MYL3 | c.435T= (p.Asn145=) n.657T= n.393T= | |
3 | g.46859521A>C | CA352495987 | MYL3 | c.435T>G (p.Asn145Lys) n.657T>G n.393T>G | |
3 | g.46859521A>G | CA044149 | MYL3 | c.435T>C (p.Asn145=) n.657T>C n.393T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.46859521A>T | CA16042471 | MYL3 | c.435T>A (p.Asn145Lys) n.657T>A n.393T>A | ClinVar dbSNP |
3 | g.46859522T>A | CA352495993 | MYL3 | c.434A>T (p.Asn145Ile) n.656A>T n.392A>T | |
3 | g.46859522T>C | CA352495995 | MYL3 | c.434A>G (p.Asn145Ser) n.656A>G n.392A>G | |
3 | g.46859522T>G | CA352495998 | MYL3 | c.434A>C (p.Asn145Thr) n.656A>C n.392A>C | ClinVar |