Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49451517_49451518delinsTA | CA2580074725 | MMUT | c.1280_1281delinsTA (p.Gly427Val) | ClinVar |
6 | g.49451518C>A | CA364398737 | MMUT | c.1280G>T (p.Gly427Val) | |
6 | g.49451518C= | CA1627389301 | MMUT | c.1280G= (p.Gly427=) | |
6 | g.49451518C>G | CA364398738 | MMUT | c.1280G>C (p.Gly427Ala) | |
6 | g.49451518C>T | CA347873 | MMUT | c.1280G>A (p.Gly427Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451519C>A | CA364398739 | MMUT | c.1279G>T (p.Gly427Cys) | |
6 | g.49451519C= | CA1627389302 | MMUT | c.1279G= (p.Gly427=) | |
6 | g.49451519C>G | CA364398740 | MMUT | c.1279G>C (p.Gly427Arg) | |
6 | g.49451519C>T | CA364398741 | MMUT | c.1279G>A (p.Gly427Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451520T>A | CA3846927 | MMUT | c.1278A>T (p.Gly426=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451520T>C | CA450606216 | MMUT | c.1278A>G (p.Gly426=) | |
6 | g.49451520T>G | CA450606217 | MMUT | c.1278A>C (p.Gly426=) | |
6 | g.49451520T= | CA1627389303 | MMUT | c.1278A= (p.Gly426=) | |
6 | g.49451521C>A | CA364398742 | MMUT | c.1277G>T (p.Gly426Val) | gnomAD v4 |
6 | g.49451521C= | CA1627389304 | MMUT | c.1277G= (p.Gly426=) | |
6 | g.49451521C>G | CA138796331 | MMUT | c.1277G>C (p.Gly426Ala) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.49451521C>T | CA10575866 | MMUT | c.1277G>A (p.Gly426Glu) | ClinVar dbSNP |
6 | g.49451522C>A | CA364398743 | MMUT | c.1276G>T (p.Gly426Ter) | |
6 | g.49451522C= | CA1627389305 | MMUT | c.1276G= (p.Gly426=) | |
6 | g.49451522C>G | CA364398744 | MMUT | c.1276G>C (p.Gly426Arg) | |
6 | g.49451522C>T | CA138796335 | MMUT | c.1276G>A (p.Gly426Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49451523C>A | CA364398745 | MMUT | c.1275G>T (p.Trp425Cys) | |
6 | g.49451523C>G | CA364398746 | MMUT | c.1275G>C (p.Trp425Cys) | |
6 | g.49451523C>T | CA364398747 | MMUT | c.1275G>A (p.Trp425Ter) | |
6 | g.49451524C>A | CA364398748 | MMUT | c.1274G>T (p.Trp425Leu) | |
6 | g.49451524C>G | CA364398749 | MMUT | c.1274G>C (p.Trp425Ser) | |
6 | g.49451524C>T | CA364398750 | MMUT | c.1274G>A (p.Trp425Ter) | ClinVar dbSNP gnomAD v4 |
6 | g.49451525A>C | CA364398752 | MMUT | c.1273T>G (p.Trp425Gly) | |
6 | g.49451525A>G | CA364398753 | MMUT | c.1273T>C (p.Trp425Arg) | |
6 | g.49451525A>T | CA364398751 | MMUT | c.1273T>A (p.Trp425Arg) | |
6 | g.49451526A>C | CA450606242 | MMUT | c.1272T>G (p.Pro424=) | |
6 | g.49451526A>G | CA450606240 | MMUT | c.1272T>C (p.Pro424=) | ClinVar dbSNP gnomAD v4 |
6 | g.49451526A>T | CA450606239 | MMUT | c.1272T>A (p.Pro424=) | |
6 | g.49451527G>A | CA10575867 | MMUT | c.1271C>T (p.Pro424Leu) | ClinVar dbSNP |
6 | g.49451527G>C | CA364398754 | MMUT | c.1271C>G (p.Pro424Arg) | |
6 | g.49451527G= | CA1627389306 | MMUT | c.1271C= (p.Pro424=) | |
6 | g.49451527G>T | CA364398755 | MMUT | c.1271C>A (p.Pro424His) | |
6 | g.49451528del | CA2679046690 | MMUT | c.1271del (p.Pro424LeufsTer7) | gnomAD v4 |
6 | g.49451528G>A | CA3846928 | MMUT | c.1270C>T (p.Pro424Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451528G>C | CA364398756 | MMUT | c.1270C>G (p.Pro424Ala) | dbSNP gnomAD v4 |
6 | g.49451528G= | CA1627389307 | MMUT | c.1270C= (p.Pro424=) | |
6 | g.49451528G>T | CA364398757 | MMUT | c.1270C>A (p.Pro424Thr) | gnomAD v4 |
6 | g.49451529A>C | CA364398759 | MMUT | c.1269T>G (p.Asp423Glu) | |
6 | g.49451529A>G | CA450606251 | MMUT | c.1269T>C (p.Asp423=) | |
6 | g.49451529A>T | CA364398758 | MMUT | c.1269T>A (p.Asp423Glu) | |
6 | g.49451530T>A | CA364398760 | MMUT | c.1268A>T (p.Asp423Val) | |
6 | g.49451530T>C | CA364398761 | MMUT | c.1268A>G (p.Asp423Gly) | dbSNP |
6 | g.49451530T>G | CA364398762 | MMUT | c.1268A>C (p.Asp423Ala) | |
6 | g.49451530T= | CA1627389308 | MMUT | c.1268A= (p.Asp423=) | |
6 | g.49451531C>A | CA364398763 | MMUT | c.1267G>T (p.Asp423Tyr) |