Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7566377_7566383dup | CA658820637 | DSP | c.940_946dup (p.Met316AsnfsTer9) n.264_270dup | dbSNP |
6 | g.7566380C>A | CA362674755 | DSP | c.943C>A (p.Arg315Ser) n.267C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7566380C= | CA1608618826 | DSP | c.943C= (p.Arg315=) n.267C= | |
6 | g.7566380C>G | CA362674756 | DSP | c.943C>G (p.Arg315Gly) n.267C>G | |
6 | g.7566380C>T | CA007889 | DSP | c.943C>T (p.Arg315Cys) n.267C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7566381G>A | CA053316 | DSP | c.944G>A (p.Arg315His) n.268G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
6 | g.7566381G>C | CA362674757 | DSP | c.944G>C (p.Arg315Pro) n.268G>C | ClinVar |
6 | g.7566381G= | CA1608618836 | DSP | c.944G= (p.Arg315=) n.268G= | |
6 | g.7566381G>T | CA053329 | DSP | c.944G>T (p.Arg315Leu) n.268G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7566381_7566382delinsAA | CA2740094235 | DSP | c.944_945delinsAA (p.Arg315Gln) n.268_269delinsAA | ClinVar |
6 | g.7566382C>A | CA448519388 | DSP | c.945C>A (p.Arg315=) n.269C>A | |
6 | g.7566382C>G | CA448519390 | DSP | c.945C>G (p.Arg315=) n.269C>G | |
6 | g.7566382C>T | CA448519392 | DSP | c.945C>T (p.Arg315=) n.269C>T | ClinVar gnomAD v4 |
6 | g.7566383A= | CA1608618846 | DSP | c.946A= (p.Met316=) n.270A= | |
6 | g.7566383A>C | CA362674758 | DSP | c.946A>C (p.Met316Leu) n.270A>C | dbSNP gnomAD v4 |
6 | g.7566383A>G | CA053338 | DSP | c.946A>G (p.Met316Val) n.270A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7566383A>T | CA362674759 | DSP | c.946A>T (p.Met316Leu) n.270A>T | |
6 | g.7566384T>A | CA362674762 | DSP | c.947T>A (p.Met316Lys) n.271T>A | |
6 | g.7566384T>C | CA362674761 | DSP | c.947T>C (p.Met316Thr) n.271T>C | |
6 | g.7566384T>G | CA362674760 | DSP | c.947T>G (p.Met316Arg) n.271T>G | |
6 | g.7566385G>A | CA362674763 | DSP | c.948G>A (p.Met316Ile) n.272G>A | |
6 | g.7566385G>C | CA362674764 | DSP | c.948G>C (p.Met316Ile) n.272G>C | |
6 | g.7566385G>T | CA362674765 | DSP | c.948G>T (p.Met316Ile) n.272G>T | |
6 | g.7566386A>C | CA362674766 | DSP | c.949A>C (p.Ser317Arg) n.273A>C | |
6 | g.7566386A>G | CA362674767 | DSP | c.949A>G (p.Ser317Gly) n.273A>G | gnomAD v4 |
6 | g.7566386A>T | CA362674768 | DSP | c.949A>T (p.Ser317Cys) n.273A>T | |
6 | g.7566387G>A | CA362674769 | DSP | c.950G>A (p.Ser317Asn) n.274G>A | gnomAD v4 |
6 | g.7566387G>C | CA362674770 | DSP | c.950G>C (p.Ser317Thr) n.274G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.7566387G= | CA1608618863 | DSP | c.950G= (p.Ser317=) n.274G= | |
6 | g.7566387G>T | CA362674771 | DSP | c.950G>T (p.Ser317Ile) n.274G>T | |
6 | g.7566388T>A | CA362674772 | DSP | c.951T>A (p.Ser317Arg) n.275T>A | |
6 | g.7566388T>C | CA448519411 | DSP | c.951T>C (p.Ser317=) n.275T>C | |
6 | g.7566388T>G | CA362674773 | DSP | c.951T>G (p.Ser317Arg) n.275T>G | |
6 | g.7566389C>A | CA362674774 | DSP | c.952C>A (p.Gln318Lys) n.276C>A | |
6 | g.7566389C>G | CA362674775 | DSP | c.952C>G (p.Gln318Glu) n.276C>G | |
6 | g.7566389C>T | CA362674776 | DSP | c.952C>T (p.Gln318Ter) n.276C>T | |
6 | g.7566390A>C | CA362674778 | DSP | c.953A>C (p.Gln318Pro) n.277A>C | |
6 | g.7566390A>G | CA362674779 | DSP | c.953A>G (p.Gln318Arg) n.277A>G | |
6 | g.7566390A>T | CA362674777 | DSP | c.953A>T (p.Gln318Leu) n.277A>T | |
6 | g.7566391A= | CA1608618869 | DSP | c.954A= (p.Gln318=) n.278A= | |
6 | g.7566391A>C | CA362674780 | DSP | c.954A>C (p.Gln318His) n.278A>C | ClinVar dbSNP |
6 | g.7566391A>G | CA133955193 | DSP | c.954A>G (p.Gln318=) n.278A>G | dbSNP |
6 | g.7566391A>T | CA362674781 | DSP | c.954A>T (p.Gln318His) n.278A>T | |
6 | g.7566392C>A | CA362674782 | DSP | c.955C>A (p.Leu319Met) n.279C>A | |
6 | g.7566392C= | CA1608618874 | DSP | c.955C= (p.Leu319=) n.279C= | |
6 | g.7566392C>G | CA16611949 | DSP | c.955C>G (p.Leu319Val) n.279C>G | ClinVar dbSNP |
6 | g.7566392C>T | CA053356 | DSP | c.955C>T (p.Leu319=) n.279C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7566393T>A | CA362674783 | DSP | c.956T>A (p.Leu319Gln) n.280T>A | |
6 | g.7566393T>C | CA362674784 | DSP | c.956T>C (p.Leu319Pro) n.280T>C | ClinVar |
6 | g.7566393T>G | CA362674785 | DSP | c.956T>G (p.Leu319Arg) n.280T>G |