| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28028203G>A | CA483043296 | FLT3 | c.2028C>T (p.Asn676=) n.2110C>T c.1971C>T (p.Asn657=) c.1503C>T (p.Asn501=) c.1812C>T (p.Asn604=) c.1149C>T (p.Asn383=) c.1131C>T (p.Asn377=) n.2094C>T | dbSNP gnomAD v4 |
| 13 | g.28028203G>C | CA16602567 | FLT3 | c.2028C>G (p.Asn676Lys) n.2110C>G c.1971C>G (p.Asn657Lys) c.1503C>G (p.Asn501Lys) c.1812C>G (p.Asn604Lys) c.1149C>G (p.Asn383Lys) c.1131C>G (p.Asn377Lys) n.2094C>G | ClinVar dbSNP COSMIC |
| 13 | g.28028203G>T | CA16602568 | FLT3 | c.2028C>A (p.Asn676Lys) n.2110C>A c.1971C>A (p.Asn657Lys) c.1503C>A (p.Asn501Lys) c.1812C>A (p.Asn604Lys) c.1149C>A (p.Asn383Lys) c.1131C>A (p.Asn377Lys) n.2094C>A | ClinVar dbSNP gnomAD v4 COSMIC |