Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7579953A= | CA1608615307 | DSP | c.3763A= (p.Arg1255=) c.3582+181A= (n.3582+181A=) | |
6 | g.7579953A>C | CA448714771 | DSP | c.3763A>C (p.Arg1255=) c.3582+181A>C (n.3582+181A>C) | |
6 | g.7579953A>G | CA362684802 | DSP | c.3763A>G (p.Arg1255Gly) c.3582+181A>G (n.3582+181A>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.7579953A>T | CA362684803 | DSP | c.3763A>T (p.Arg1255Trp) c.3582+181A>T (n.3582+181A>T) | |
6 | g.7579954G>A | CA038944 | DSP | c.3764G>A (p.Arg1255Lys) c.3582+182G>A (n.3582+182G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7579954G>C | CA038954 | DSP | c.3764G>C (p.Arg1255Thr) c.3582+182G>C (n.3582+182G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7579954G= | CA1608615315 | DSP | c.3764G= (p.Arg1255=) c.3582+182G= (n.3582+182G=) | |
6 | g.7579954G>T | CA362684804 | DSP | c.3764G>T (p.Arg1255Met) c.3582+182G>T (n.3582+182G>T) | gnomAD v4 |
6 | g.7579955G>A | CA448714779 | DSP | c.3765G>A (p.Arg1255=) c.3582+183G>A (n.3582+183G>A) | |
6 | g.7579955G>C | CA362684805 | DSP | c.3765G>C (p.Arg1255Ser) c.3582+183G>C (n.3582+183G>C) | gnomAD v4 |
6 | g.7579955G>T | CA362684806 | DSP | c.3765G>T (p.Arg1255Ser) c.3582+183G>T (n.3582+183G>T) | |
6 | g.7579956C>A | CA362684807 | DSP | c.3766C>A (p.Leu1256Ile) c.3582+184C>A (n.3582+184C>A) | COSMIC |
6 | g.7579956C= | CA1608615327 | DSP | c.3766C= (p.Leu1256=) c.3582+184C= (n.3582+184C=) | |
6 | g.7579956C>G | CA362684808 | DSP | c.3766C>G (p.Leu1256Val) c.3582+184C>G (n.3582+184C>G) | |
6 | g.7579956C>T | CA038972 | DSP | c.3766C>T (p.Leu1256Phe) c.3582+184C>T (n.3582+184C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7579957T>A | CA362684809 | DSP | c.3767T>A (p.Leu1256His) c.3582+185T>A (n.3582+185T>A) | gnomAD v4 |
6 | g.7579957T>C | CA362684810 | DSP | c.3767T>C (p.Leu1256Pro) c.3582+185T>C (n.3582+185T>C) | |
6 | g.7579957T>G | CA362684811 | DSP | c.3767T>G (p.Leu1256Arg) c.3582+185T>G (n.3582+185T>G) | |
6 | g.7579958C>A | CA448714787 | DSP | c.3768C>A (p.Leu1256=) c.3582+186C>A (n.3582+186C>A) | |
6 | g.7579958C= | CA1608615333 | DSP | c.3768C= (p.Leu1256=) c.3582+186C= (n.3582+186C=) | |
6 | g.7579958C>G | CA448714788 | DSP | c.3768C>G (p.Leu1256=) c.3582+186C>G (n.3582+186C>G) | |
6 | g.7579958C>T | CA133968739 | DSP | c.3768C>T (p.Leu1256=) c.3582+186C>T (n.3582+186C>T) | dbSNP |
6 | g.7579959A>C | CA362684812 | DSP | c.3769A>C (p.Asn1257His) c.3582+187A>C (n.3582+187A>C) | |
6 | g.7579959A>G | CA362684813 | DSP | c.3769A>G (p.Asn1257Asp) c.3582+187A>G (n.3582+187A>G) | |
6 | g.7579959A>T | CA362684814 | DSP | c.3769A>T (p.Asn1257Tyr) c.3582+187A>T (n.3582+187A>T) | |
6 | g.7579960A= | CA1608615336 | DSP | c.3770A= (p.Asn1257=) c.3582+188A= (n.3582+188A=) | |
6 | g.7579960A>C | CA362684815 | DSP | c.3770A>C (p.Asn1257Thr) c.3582+188A>C (n.3582+188A>C) | |
6 | g.7579960A>G | CA362684816 | DSP | c.3770A>G (p.Asn1257Ser) c.3582+188A>G (n.3582+188A>G) | ClinVar dbSNP gnomAD v4 |
6 | g.7579960A>T | CA362684817 | DSP | c.3770A>T (p.Asn1257Ile) c.3582+188A>T (n.3582+188A>T) | |
6 | g.7579961T>A | CA362684818 | DSP | c.3771T>A (p.Asn1257Lys) c.3582+189T>A (n.3582+189T>A) | gnomAD v4 |
6 | g.7579961T>C | CA448714791 | DSP | c.3771T>C (p.Asn1257=) c.3582+189T>C (n.3582+189T>C) | gnomAD v4 |
6 | g.7579961T>G | CA362684819 | DSP | c.3771T>G (p.Asn1257Lys) c.3582+189T>G (n.3582+189T>G) | |
6 | g.7579962G>A | CA362684822 | DSP | c.3772G>A (p.Asp1258Asn) c.3582+190G>A (n.3582+190G>A) | |
6 | g.7579962G>C | CA362684820 | DSP | c.3772G>C (p.Asp1258His) c.3582+190G>C (n.3582+190G>C) | |
6 | g.7579962G>T | CA362684821 | DSP | c.3772G>T (p.Asp1258Tyr) c.3582+190G>T (n.3582+190G>T) | COSMIC |
6 | g.7579963A>C | CA362684823 | DSP | c.3773A>C (p.Asp1258Ala) c.3582+191A>C (n.3582+191A>C) | |
6 | g.7579963A>G | CA362684824 | DSP | c.3773A>G (p.Asp1258Gly) c.3582+191A>G (n.3582+191A>G) | |
6 | g.7579963A>T | CA362684825 | DSP | c.3773A>T (p.Asp1258Val) c.3582+191A>T (n.3582+191A>T) | |
6 | g.7579964C>A | CA038986 | DSP | c.3774C>A (p.Asp1258Glu) c.3582+192C>A (n.3582+192C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7579964C= | CA1608615345 | DSP | c.3774C= (p.Asp1258=) c.3582+192C= (n.3582+192C=) | |
6 | g.7579964C>G | CA362684826 | DSP | c.3774C>G (p.Asp1258Glu) c.3582+192C>G (n.3582+192C>G) | |
6 | g.7579964C>T | CA448714800 | DSP | c.3774C>T (p.Asp1258=) c.3582+192C>T (n.3582+192C>T) | |
6 | g.7579965A= | CA1608615361 | DSP | c.3775A= (p.Ser1259=) c.3582+193A= (n.3582+193A=) | |
6 | g.7579965A>C | CA362684827 | DSP | c.3775A>C (p.Ser1259Arg) c.3582+193A>C (n.3582+193A>C) | |
6 | g.7579965A>G | CA039000 | DSP | c.3775A>G (p.Ser1259Gly) c.3582+193A>G (n.3582+193A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7579965A>T | CA362684828 | DSP | c.3775A>T (p.Ser1259Cys) c.3582+193A>T (n.3582+193A>T) | |
6 | g.7579966G>A | CA362684829 | DSP | c.3776G>A (p.Ser1259Asn) c.3582+194G>A (n.3582+194G>A) | gnomAD v4 |
6 | g.7579966G>C | CA362684831 | DSP | c.3776G>C (p.Ser1259Thr) c.3582+194G>C (n.3582+194G>C) | |
6 | g.7579966G>T | CA362684830 | DSP | c.3776G>T (p.Ser1259Ile) c.3582+194G>T (n.3582+194G>T) | |
6 | g.7579967C>A | CA362684832 | DSP | c.3777C>A (p.Ser1259Arg) c.3582+195C>A (n.3582+195C>A) |