Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.88437437C>A | CA397125333 | ZNF469 | c.9967C>A (p.Leu3323Met) c.9883C>A (p.Leu3295Met) | |
16 | g.88437437C= | CA2241073090 | ZNF469 | c.9967C= (p.Leu3323=) c.9883C= (p.Leu3295=) | |
16 | g.88437437C>G | CA397125330 | ZNF469 | c.9967C>G (p.Leu3323Val) c.9883C>G (p.Leu3295Val) | gnomAD v4 |
16 | g.88437437C>T | CA286386015 | ZNF469 | c.9967C>T (p.Leu3323=) c.9883C>T (p.Leu3295=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.88437438T>A | CA397125334 | ZNF469 | c.9968T>A (p.Leu3323Gln) c.9884T>A (p.Leu3295Gln) | |
16 | g.88437438T>C | CA397125337 | ZNF469 | c.9968T>C (p.Leu3323Pro) c.9884T>C (p.Leu3295Pro) | |
16 | g.88437438T>G | CA397125339 | ZNF469 | c.9968T>G (p.Leu3323Arg) c.9884T>G (p.Leu3295Arg) | |
16 | g.88437439G>A | CA497358574 | ZNF469 | c.9969G>A (p.Leu3323=) c.9885G>A (p.Leu3295=) | gnomAD v4 |
16 | g.88437439G>C | CA497358575 | ZNF469 | c.9969G>C (p.Leu3323=) c.9885G>C (p.Leu3295=) | |
16 | g.88437439G>T | CA497358576 | ZNF469 | c.9969G>T (p.Leu3323=) c.9885G>T (p.Leu3295=) | |
16 | g.88437440C>A | CA397125341 | ZNF469 | c.9970C>A (p.Gln3324Lys) c.9886C>A (p.Gln3296Lys) | gnomAD v4 |
16 | g.88437440C= | CA2241073091 | ZNF469 | c.9970C= (p.Gln3324=) c.9886C= (p.Gln3296=) | |
16 | g.88437440C>G | CA286386039 | ZNF469 | c.9970C>G (p.Gln3324Glu) c.9886C>G (p.Gln3296Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.88437440C>T | CA397125344 | ZNF469 | c.9970C>T (p.Gln3324Ter) c.9886C>T (p.Gln3296Ter) | |
16 | g.88437441A= | CA2241073093 | ZNF469 | c.9971A= (p.Gln3324=) c.9887A= (p.Gln3296=) | |
16 | g.88437441A>C | CA397125347 | ZNF469 | c.9971A>C (p.Gln3324Pro) c.9887A>C (p.Gln3296Pro) | |
16 | g.88437441A>G | CA397125345 | ZNF469 | c.9971A>G (p.Gln3324Arg) c.9887A>G (p.Gln3296Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.88437441A>T | CA397125346 | ZNF469 | c.9971A>T (p.Gln3324Leu) c.9887A>T (p.Gln3296Leu) | |
16 | g.88437442A>C | CA397125348 | ZNF469 | c.9972A>C (p.Gln3324His) c.9888A>C (p.Gln3296His) | |
16 | g.88437442A>G | CA497358577 | ZNF469 | c.9972A>G (p.Gln3324=) c.9888A>G (p.Gln3296=) | |
16 | g.88437442A>T | CA397125349 | ZNF469 | c.9972A>T (p.Gln3324His) c.9888A>T (p.Gln3296His) | |
16 | g.88437443G>A | CA397125350 | ZNF469 | c.9973G>A (p.Ala3325Thr) c.9889G>A (p.Ala3297Thr) | |
16 | g.88437443G>C | CA397125351 | ZNF469 | c.9973G>C (p.Ala3325Pro) c.9889G>C (p.Ala3297Pro) | |
16 | g.88437443G= | CA2241073094 | ZNF469 | c.9973G= (p.Ala3325=) c.9889G= (p.Ala3297=) | |
16 | g.88437443G>T | CA397125352 | ZNF469 | c.9973G>T (p.Ala3325Ser) c.9889G>T (p.Ala3297Ser) | dbSNP gnomAD v2 |
16 | g.88437445_88437466del | CA2634824447 | ZNF469 | c.9975_9996del (p.Thr3326ArgfsTer?) c.9891_9912del (p.Thr3298ArgfsTer?) | gnomAD v4 |
16 | g.88437444C>A | CA397125353 | ZNF469 | c.9974C>A (p.Ala3325Asp) c.9890C>A (p.Ala3297Asp) | |
16 | g.88437444C>G | CA397125355 | ZNF469 | c.9974C>G (p.Ala3325Gly) c.9890C>G (p.Ala3297Gly) | |
16 | g.88437444C>T | CA397125354 | ZNF469 | c.9974C>T (p.Ala3325Val) c.9890C>T (p.Ala3297Val) | gnomAD v4 |
16 | g.88437445C>A | CA497358578 | ZNF469 | c.9975C>A (p.Ala3325=) c.9891C>A (p.Ala3297=) | gnomAD v4 |
16 | g.88437445C>G | CA497358579 | ZNF469 | c.9975C>G (p.Ala3325=) c.9891C>G (p.Ala3297=) | |
16 | g.88437445C>T | CA497358580 | ZNF469 | c.9975C>T (p.Ala3325=) c.9891C>T (p.Ala3297=) | |
16 | g.88437446A= | CA2241073096 | ZNF469 | c.9976A= (p.Thr3326=) c.9892A= (p.Thr3298=) | |
16 | g.88437446A>C | CA397125356 | ZNF469 | c.9976A>C (p.Thr3326Pro) c.9892A>C (p.Thr3298Pro) | gnomAD v4 |
16 | g.88437446A>G | CA397125357 | ZNF469 | c.9976A>G (p.Thr3326Ala) c.9892A>G (p.Thr3298Ala) | dbSNP |
16 | g.88437446A>T | CA397125358 | ZNF469 | c.9976A>T (p.Thr3326Ser) c.9892A>T (p.Thr3298Ser) | |
16 | g.88437447C>A | CA397125359 | ZNF469 | c.9977C>A (p.Thr3326Asn) c.9893C>A (p.Thr3298Asn) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.88437447C= | CA2241073099 | ZNF469 | c.9977C= (p.Thr3326=) c.9893C= (p.Thr3298=) | |
16 | g.88437447C>G | CA397125360 | ZNF469 | c.9977C>G (p.Thr3326Ser) c.9893C>G (p.Thr3298Ser) | gnomAD v4 |
16 | g.88437447C>T | CA397125361 | ZNF469 | c.9977C>T (p.Thr3326Ile) c.9893C>T (p.Thr3298Ile) | dbSNP gnomAD v4 |
16 | g.88437450del | CA2634824448 | ZNF469 | c.9980del (p.Pro3327ArgfsTer?) c.9896del (p.Pro3299ArgfsTer?) | gnomAD v4 |
16 | g.88437448C>A | CA497358581 | ZNF469 | c.9978C>A (p.Thr3326=) c.9894C>A (p.Thr3298=) | |
16 | g.88437448C>G | CA497358583 | ZNF469 | c.9978C>G (p.Thr3326=) c.9894C>G (p.Thr3298=) | gnomAD v4 COSMIC |
16 | g.88437448C>T | CA497358582 | ZNF469 | c.9978C>T (p.Thr3326=) c.9894C>T (p.Thr3298=) | gnomAD v4 |
16 | g.88437449C>A | CA397125362 | ZNF469 | c.9979C>A (p.Pro3327Thr) c.9895C>A (p.Pro3299Thr) | gnomAD v4 |
16 | g.88437449C>G | CA397125363 | ZNF469 | c.9979C>G (p.Pro3327Ala) c.9895C>G (p.Pro3299Ala) | gnomAD v4 |
16 | g.88437449C>T | CA397125364 | ZNF469 | c.9979C>T (p.Pro3327Ser) c.9895C>T (p.Pro3299Ser) | gnomAD v4 |
16 | g.88437450C>A | CA397125365 | ZNF469 | c.9980C>A (p.Pro3327Gln) c.9896C>A (p.Pro3299Gln) | |
16 | g.88437450C= | CA2241073101 | ZNF469 | c.9980C= (p.Pro3327=) c.9896C= (p.Pro3299=) | |
16 | g.88437450C>G | CA397125366 | ZNF469 | c.9980C>G (p.Pro3327Arg) c.9896C>G (p.Pro3299Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |