| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.27198258C>A | CA367069656 | HOXA13 | c.1107G>T (p.Trp369Cys) | dbSNP |
| 7 | g.27198258C= | CA1696263322 | HOXA13 | c.1107G= (p.Trp369=) | |
| 7 | g.27198258C>G | CA367069657 | HOXA13 | c.1107G>C (p.Trp369Cys) | dbSNP |
| 7 | g.27198258C>T | CA257393 | HOXA13 | c.1107G>A (p.Trp369Ter) | ClinVar dbSNP |
| 7 | g.27198259C>A | CA367069658 | HOXA13 | c.1106G>T (p.Trp369Leu) | dbSNP |
| 7 | g.27198259C>G | CA367069659 | HOXA13 | c.1106G>C (p.Trp369Ser) | dbSNP |
| 7 | g.27198259C>T | CA367069660 | HOXA13 | c.1106G>A (p.Trp369Ter) | dbSNP |
| 7 | g.27198260A>C | CA367069661 | HOXA13 | c.1105T>G (p.Trp369Gly) | gnomAD v4 |
| 7 | g.27198260A>G | CA367069662 | HOXA13 | c.1105T>C (p.Trp369Arg) | |
| 7 | g.27198260A>T | CA367069663 | HOXA13 | c.1105T>A (p.Trp369Arg) | dbSNP |
| 7 | g.27198261G>A | CA454513091 | HOXA13 | c.1104C>T (p.Ile368=) | dbSNP |
| 7 | g.27198261G>C | CA367069664 | HOXA13 | c.1104C>G (p.Ile368Met) | dbSNP COSMIC |
| 7 | g.27198261G>T | CA454513093 | HOXA13 | c.1104C>A (p.Ile368=) | |
| 7 | g.27198262A= | CA1696263331 | HOXA13 | c.1103T= (p.Ile368=) | |
| 7 | g.27198262A>C | CA367069667 | HOXA13 | c.1103T>G (p.Ile368Ser) | |
| 7 | g.27198262A>G | CA367069666 | HOXA13 | c.1103T>C (p.Ile368Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.27198262A>T | CA367069665 | HOXA13 | c.1103T>A (p.Ile368Asn) | dbSNP |
| 7 | g.27198263T>A | CA367069668 | HOXA13 | c.1102A>T (p.Ile368Phe) | dbSNP |
| 7 | g.27198263T>C | CA367069670 | HOXA13 | c.1102A>G (p.Ile368Val) | dbSNP |
| 7 | g.27198263T>G | CA367069669 | HOXA13 | c.1102A>C (p.Ile368Leu) | |
| 7 | g.27198264T>A | CA454513096 | HOXA13 | c.1101A>T (p.Thr367=) | dbSNP |
| 7 | g.27198264T>C | CA4198545 | HOXA13 | c.1101A>G (p.Thr367=) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 7 | g.27198264T>G | CA454513097 | HOXA13 | c.1101A>C (p.Thr367=) | |
| 7 | g.27198264T= | CA1696263343 | HOXA13 | c.1101A= (p.Thr367=) | |
| 7 | g.27198265G>A | CA367069671 | HOXA13 | c.1100C>T (p.Thr367Ile) | dbSNP |
| 7 | g.27198265G>C | CA367069672 | HOXA13 | c.1100C>G (p.Thr367Arg) | dbSNP |
| 7 | g.27198265G>T | CA367069673 | HOXA13 | c.1100C>A (p.Thr367Lys) | dbSNP |
| 7 | g.27198266T>A | CA367069674 | HOXA13 | c.1099A>T (p.Thr367Ser) | dbSNP |
| 7 | g.27198266T>C | CA367069675 | HOXA13 | c.1099A>G (p.Thr367Ala) | |
| 7 | g.27198266T>G | CA367069676 | HOXA13 | c.1099A>C (p.Thr367Pro) | dbSNP |
| 7 | g.27198267G>A | CA454513102 | HOXA13 | c.1098C>T (p.Val366=) | dbSNP |
| 7 | g.27198267G>C | CA454513103 | HOXA13 | c.1098C>G (p.Val366=) | dbSNP |
| 7 | g.27198267G>T | CA454513104 | HOXA13 | c.1098C>A (p.Val366=) | dbSNP |
| 7 | g.27198268A= | CA1696263346 | HOXA13 | c.1097T= (p.Val366=) | |
| 7 | g.27198268A>C | CA4198546 | HOXA13 | c.1097T>G (p.Val366Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.27198268A>G | CA367069677 | HOXA13 | c.1097T>C (p.Val366Ala) | dbSNP |
| 7 | g.27198268A>T | CA367069678 | HOXA13 | c.1097T>A (p.Val366Asp) | dbSNP |
| 7 | g.27198269C>A | CA367069679 | HOXA13 | c.1096G>T (p.Val366Phe) | |
| 7 | g.27198269C>G | CA367069680 | HOXA13 | c.1096G>C (p.Val366Leu) | dbSNP gnomAD v4 |
| 7 | g.27198269C>T | CA367069681 | HOXA13 | c.1096G>A (p.Val366Ile) | dbSNP COSMIC |
| 7 | g.27198270C>A | CA367069683 | HOXA13 | c.1095G>T (p.Gln365His) | |
| 7 | g.27198270C= | CA1696263351 | HOXA13 | c.1095G= (p.Gln365=) | |
| 7 | g.27198270C>G | CA367069682 | HOXA13 | c.1095G>C (p.Gln365His) | |
| 7 | g.27198270C>T | CA4198547 | HOXA13 | c.1095G>A (p.Gln365=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.27198271T>A | CA367069684 | HOXA13 | c.1094A>T (p.Gln365Leu) | dbSNP |
| 7 | g.27198271T>C | CA367069685 | HOXA13 | c.1094A>G (p.Gln365Arg) | dbSNP |
| 7 | g.27198271T>G | CA367069686 | HOXA13 | c.1094A>C (p.Gln365Pro) | dbSNP |
| 7 | g.27198272G>A | CA367069687 | HOXA13 | c.1093C>T (p.Gln365Ter) | dbSNP |
| 7 | g.27198272G>C | CA367069688 | HOXA13 | c.1093C>G (p.Gln365Glu) | dbSNP |
| 7 | g.27198272G>T | CA367069689 | HOXA13 | c.1093C>A (p.Gln365Lys) |