Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.15540434C>A | CA2576657818 | CYP4F22 | c.672-16C>A (n.672-16C>A) | |
19 | g.15540434C= | CA2324927878 | CYP4F22 | c.672-16C= (n.672-16C=) | |
19 | g.15540434C>T | CA9269668 | CYP4F22 | c.672-16C>T (n.672-16C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.15540436C= | CA2324927879 | CYP4F22 | c.672-14C= (n.672-14C=) | |
19 | g.15540436C>T | CA631955853 | CYP4F22 | c.672-14C>T (n.672-14C>T) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.15540437T>C | CA2813739713 | CYP4F22 | c.672-13T>C (n.672-13T>C) | |
19 | g.15540438T>C | CA9269669 | CYP4F22 | c.672-12T>C (n.672-12T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.15540438T= | CA2324927880 | CYP4F22 | c.672-12T= (n.672-12T=) | |
19 | g.15540439C>G | CA2583107995 | CYP4F22 | c.672-11C>G (n.672-11C>G) | gnomAD v4 |
19 | g.15540439C>T | CA2576657819 | CYP4F22 | c.672-11C>T (n.672-11C>T) | gnomAD v4 |
19 | g.15540441C= | CA2324927881 | CYP4F22 | c.672-9C= (n.672-9C=) | |
19 | g.15540441C>G | CA2583107996 | CYP4F22 | c.672-9C>G (n.672-9C>G) | gnomAD v4 |
19 | g.15540441C>T | CA9269670 | CYP4F22 | c.672-9C>T (n.672-9C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.15540442C>A | CA2583107997 | CYP4F22 | c.672-8C>A (n.672-8C>A) | gnomAD v4 |
19 | g.15540442C= | CA2324927882 | CYP4F22 | c.672-8C= (n.672-8C=) | |
19 | g.15540442C>G | CA305826100 | CYP4F22 | c.672-8C>G (n.672-8C>G) | dbSNP |
19 | g.15540442C>T | CA2583107998 | CYP4F22 | c.672-8C>T (n.672-8C>T) | gnomAD v4 |
19 | g.15540444T>C | CA9269671 | CYP4F22 | c.672-6T>C (n.672-6T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.15540444T= | CA2324927883 | CYP4F22 | c.672-6T= (n.672-6T=) | |
19 | g.15540446G>A | CA2324927885 | CYP4F22 | c.672-4G>A (n.672-4G>A) | dbSNP |
19 | g.15540446G= | CA2324927884 | CYP4F22 | c.672-4G= (n.672-4G=) | |
19 | g.15540448A>C | CA404535295 | CYP4F22 | c.672-2A>C (n.672-2A>C) | |
19 | g.15540448A>G | CA404535297 | CYP4F22 | c.672-2A>G (n.672-2A>G) | |
19 | g.15540448A>T | CA404535299 | CYP4F22 | c.672-2A>T (n.672-2A>T) | |
19 | g.15540449G>A | CA404535300 | CYP4F22 | c.672-1G>A (n.672-1G>A) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.15540449G>C | CA404535301 | CYP4F22 | c.672-1G>C (n.672-1G>C) | |
19 | g.15540449G= | CA2324927886 | CYP4F22 | c.672-1G= (n.672-1G=) | |
19 | g.15540449G>T | CA404535302 | CYP4F22 | c.672-1G>T (n.672-1G>T) | |
19 | g.15540450G>A | CA9269672 | CYP4F22 | c.672G>A (p.Glu224=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.15540450G>C | CA404535305 | CYP4F22 | c.672G>C (p.Glu224Asp) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.15540450G= | CA2324927887 | CYP4F22 | c.672G= (p.Glu224=) | |
19 | g.15540450G>T | CA404535307 | CYP4F22 | c.672G>T (p.Glu224Asp) | |
19 | g.15540451A= | CA2324927888 | CYP4F22 | c.673A= (p.Lys225=) | |
19 | g.15540451A>C | CA404535314 | CYP4F22 | c.673A>C (p.Lys225Gln) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.15540451A>G | CA404535312 | CYP4F22 | c.673A>G (p.Lys225Glu) | |
19 | g.15540451A>T | CA404535309 | CYP4F22 | c.673A>T (p.Lys225Ter) | |
19 | g.15540452A= | CA2324927889 | CYP4F22 | c.674A= (p.Lys225=) | |
19 | g.15540452A>C | CA404535316 | CYP4F22 | c.674A>C (p.Lys225Thr) | |
19 | g.15540452A>G | CA9269673 | CYP4F22 | c.674A>G (p.Lys225Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.15540452A>T | CA404535318 | CYP4F22 | c.674A>T (p.Lys225Met) | |
19 | g.15540453G>A | CA505828129 | CYP4F22 | c.675G>A (p.Lys225=) | |
19 | g.15540453G>C | CA404535320 | CYP4F22 | c.675G>C (p.Lys225Asn) | |
19 | g.15540453G>T | CA404535321 | CYP4F22 | c.675G>T (p.Lys225Asn) | COSMIC |
19 | g.15540454A= | CA2324927890 | CYP4F22 | c.676A= (p.Met226=) | |
19 | g.15540454A>C | CA404535328 | CYP4F22 | c.676A>C (p.Met226Leu) | |
19 | g.15540454A>G | CA404535325 | CYP4F22 | c.676A>G (p.Met226Val) | |
19 | g.15540454A>T | CA404535323 | CYP4F22 | c.676A>T (p.Met226Leu) | dbSNP gnomAD v4 |
19 | g.15540455T>A | CA404535330 | CYP4F22 | c.677T>A (p.Met226Lys) | |
19 | g.15540455T>C | CA404535332 | CYP4F22 | c.677T>C (p.Met226Thr) | |
19 | g.15540455T>G | CA404535334 | CYP4F22 | c.677T>G (p.Met226Arg) |