Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129530962del | CA645514953 | RHO | c.448del (p.Glu150ArgfsTer?) | COSMIC |
3 | g.129530962G>A | CA122824 | RHO | c.448G>A (p.Glu150Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530962G>C | CA2607161 | RHO | c.448G>C (p.Glu150Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530962G= | CA1401209417 | RHO | c.448G= (p.Glu150=) | |
3 | g.129530962G>T | CA354498282 | RHO | c.448G>T (p.Glu150Ter) | |
3 | g.129530963A>C | CA354498284 | RHO | c.449A>C (p.Glu150Ala) | |
3 | g.129530963A>G | CA354498286 | RHO | c.449A>G (p.Glu150Gly) | |
3 | g.129530963A>T | CA354498290 | RHO | c.449A>T (p.Glu150Val) | |
3 | g.129530964G>A | CA435643952 | RHO | c.450G>A (p.Glu150=) | |
3 | g.129530964G>C | CA354498294 | RHO | c.450G>C (p.Glu150Asp) | dbSNP gnomAD v4 |
3 | g.129530964G= | CA1401209423 | RHO | c.450G= (p.Glu150=) | |
3 | g.129530964G>T | CA354498295 | RHO | c.450G>T (p.Glu150Asp) | |
3 | g.129530965A>C | CA354498296 | RHO | c.451A>C (p.Asn151His) | |
3 | g.129530965A>G | CA354498301 | RHO | c.451A>G (p.Asn151Asp) | |
3 | g.129530965A>T | CA354498298 | RHO | c.451A>T (p.Asn151Tyr) | |
3 | g.129530966A= | CA1401209428 | RHO | c.452A= (p.Asn151=) | |
3 | g.129530966A>C | CA354498304 | RHO | c.452A>C (p.Asn151Thr) | |
3 | g.129530966A>G | CA354498309 | RHO | c.452A>G (p.Asn151Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530966A>T | CA354498306 | RHO | c.452A>T (p.Asn151Ile) | |
3 | g.129530967C>A | CA354498312 | RHO | c.453C>A (p.Asn151Lys) | |
3 | g.129530967C>G | CA354498315 | RHO | c.453C>G (p.Asn151Lys) | |
3 | g.129530967C>T | CA435643964 | RHO | c.453C>T (p.Asn151=) | dbSNP gnomAD v4 |
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) |