Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129530968C>A | CA354498318 | RHO | c.454C>A (p.His152Asn) | |
3 | g.129530968C= | CA1401209432 | RHO | c.454C= (p.His152=) | |
3 | g.129530968C>G | CA354498321 | RHO | c.454C>G (p.His152Asp) | |
3 | g.129530968C>T | CA354498322 | RHO | c.454C>T (p.His152Tyr) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530969A>C | CA354498324 | RHO | c.455A>C (p.His152Pro) | |
3 | g.129530969A>G | CA354498330 | RHO | c.455A>G (p.His152Arg) | gnomAD v4 |
3 | g.129530969A>T | CA354498336 | RHO | c.455A>T (p.His152Leu) | |
3 | g.129530970T>A | CA354498340 | RHO | c.456T>A (p.His152Gln) | |
3 | g.129530970T>C | CA435643976 | RHO | c.456T>C (p.His152=) | dbSNP gnomAD v4 |
3 | g.129530970T>G | CA354498344 | RHO | c.456T>G (p.His152Gln) | gnomAD v4 |
3 | g.129530971G>A | CA354498352 | RHO | c.457G>A (p.Ala153Thr) | dbSNP gnomAD v2 |
3 | g.129530971G>C | CA354498357 | RHO | c.457G>C (p.Ala153Pro) | |
3 | g.129530971G= | CA1401209436 | RHO | c.457G= (p.Ala153=) | |
3 | g.129530971G>T | CA354498359 | RHO | c.457G>T (p.Ala153Ser) | |
3 | g.129530972C>A | CA354498362 | RHO | c.458C>A (p.Ala153Asp) | ClinVar dbSNP |
3 | g.129530972C= | CA1401209444 | RHO | c.458C= (p.Ala153=) | |
3 | g.129530972C>G | CA354498365 | RHO | c.458C>G (p.Ala153Gly) | COSMIC |
3 | g.129530972C>T | CA354498363 | RHO | c.458C>T (p.Ala153Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530973C>A | CA435643986 | RHO | c.459C>A (p.Ala153=) | gnomAD v4 |
3 | g.129530973C= | CA1401209449 | RHO | c.459C= (p.Ala153=) | |
3 | g.129530973C>G | CA435643988 | RHO | c.459C>G (p.Ala153=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530973C>T | CA435643990 | RHO | c.459C>T (p.Ala153=) | dbSNP |
3 | g.129530974A>C | CA354498366 | RHO | c.460A>C (p.Ile154Leu) | |
3 | g.129530974A>G | CA354498368 | RHO | c.460A>G (p.Ile154Val) | gnomAD v4 |
3 | g.129530974A>T | CA354498370 | RHO | c.460A>T (p.Ile154Phe) | |
3 | g.129530975T>A | CA354498371 | RHO | c.461T>A (p.Ile154Asn) | |
3 | g.129530975T>C | CA354498373 | RHO | c.461T>C (p.Ile154Thr) | |
3 | g.129530975T>G | CA354498375 | RHO | c.461T>G (p.Ile154Ser) | |
3 | g.129530976C>A | CA435643999 | RHO | c.462C>A (p.Ile154=) | |
3 | g.129530976C>G | CA354498376 | RHO | c.462C>G (p.Ile154Met) | |
3 | g.129530976C>T | CA435644002 | RHO | c.462C>T (p.Ile154=) | gnomAD v4 |
3 | g.129530977A= | CA1401209452 | RHO | c.463A= (p.Met155=) | |
3 | g.129530977A>C | CA354498379 | RHO | c.463A>C (p.Met155Leu) | |
3 | g.129530977A>G | CA2607162 | RHO | c.463A>G (p.Met155Val) | dbSNP ExAC |
3 | g.129530977A>T | CA354498393 | RHO | c.463A>T (p.Met155Leu) | |
3 | g.129530978T>A | CA354498399 | RHO | c.464T>A (p.Met155Lys) | |
3 | g.129530978T>C | CA2607163 | RHO | c.464T>C (p.Met155Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530978T>G | CA354498395 | RHO | c.464T>G (p.Met155Arg) | |
3 | g.129530978T= | CA1401209457 | RHO | c.464T= (p.Met155=) | |
3 | g.129530979G>A | CA354498402 | RHO | c.465G>A (p.Met155Ile) | COSMIC |
3 | g.129530979G>C | CA354498404 | RHO | c.465G>C (p.Met155Ile) | |
3 | g.129530979G>T | CA354498406 | RHO | c.465G>T (p.Met155Ile) | |
3 | g.129530980G>A | CA354498408 | RHO | c.466G>A (p.Gly156Ser) | gnomAD v4 |
3 | g.129530980G>C | CA354498413 | RHO | c.466G>C (p.Gly156Arg) | gnomAD v4 |
3 | g.129530980G>T | CA354498415 | RHO | c.466G>T (p.Gly156Cys) | |
3 | g.129530981G>A | CA2607165 | RHO | c.467G>A (p.Gly156Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530981G>C | CA354498419 | RHO | c.467G>C (p.Gly156Ala) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530981G= | CA1401209461 | RHO | c.467G= (p.Gly156=) | |
3 | g.129530981G>T | CA2607164 | RHO | c.467G>T (p.Gly156Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530982C>A | CA435644023 | RHO | c.468C>A (p.Gly156=) |