Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129528866T>A | CA354495882 | RHO | c.133T>A (p.Phe45Ile) | |
3 | g.129528866T>C | CA256666 | RHO | c.133T>C (p.Phe45Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129528866T>G | CA354495884 | RHO | c.133T>G (p.Phe45Val) | |
3 | g.129528866T= | CA1401205403 | RHO | c.133T= (p.Phe45=) | |
3 | g.129528867T>A | CA354495886 | RHO | c.134T>A (p.Phe45Tyr) | |
3 | g.129528867T>C | CA354495888 | RHO | c.134T>C (p.Phe45Ser) | |
3 | g.129528867T>G | CA354495889 | RHO | c.134T>G (p.Phe45Cys) | |
3 | g.129528868T>A | CA354495891 | RHO | c.135T>A (p.Phe45Leu) | |
3 | g.129528868T>C | CA435768908 | RHO | c.135T>C (p.Phe45=) | dbSNP |
3 | g.129528868T>G | CA354495894 | RHO | c.135T>G (p.Phe45Leu) | |
3 | g.129528869C>A | CA354495899 | RHO | c.136C>A (p.Leu46Met) | |
3 | g.129528869C>G | CA354495902 | RHO | c.136C>G (p.Leu46Val) | |
3 | g.129528869C>T | CA435768909 | RHO | c.136C>T (p.Leu46=) | |
3 | g.129528870T>A | CA354495903 | RHO | c.137T>A (p.Leu46Gln) | |
3 | g.129528870T>C | CA354495904 | RHO | c.137T>C (p.Leu46Pro) | |
3 | g.129528870T>G | CA354495905 | RHO | c.137T>G (p.Leu46Arg) | ClinVar dbSNP |
3 | g.129528870T= | CA1401205410 | RHO | c.137T= (p.Leu46=) | |
3 | g.129528871G>A | CA435768910 | RHO | c.138G>A (p.Leu46=) | gnomAD v4 |
3 | g.129528871G>C | CA435768911 | RHO | c.138G>C (p.Leu46=) | |
3 | g.129528871G>T | CA435768912 | RHO | c.138G>T (p.Leu46=) | |
3 | g.129528872C>A | CA354495906 | RHO | c.139C>A (p.Leu47Met) | |
3 | g.129528872C= | CA1401205415 | RHO | c.139C= (p.Leu47=) | |
3 | g.129528872C>G | CA354495907 | RHO | c.139C>G (p.Leu47Val) | |
3 | g.129528872C>T | CA435768914 | RHO | c.139C>T (p.Leu47=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129528873T>A | CA354495908 | RHO | c.140T>A (p.Leu47Gln) | |
3 | g.129528873T>C | CA354495909 | RHO | c.140T>C (p.Leu47Pro) | |
3 | g.129528873T>G | CA354495910 | RHO | c.140T>G (p.Leu47Arg) | |
3 | g.129528874G>A | CA435768915 | RHO | c.141G>A (p.Leu47=) | |
3 | g.129528874G>C | CA435768916 | RHO | c.141G>C (p.Leu47=) | dbSNP |
3 | g.129528874G>T | CA435768917 | RHO | c.141G>T (p.Leu47=) | |
3 | g.129528875A>C | CA354495911 | RHO | c.142A>C (p.Ile48Leu) | |
3 | g.129528875A>G | CA354495913 | RHO | c.142A>G (p.Ile48Val) | |
3 | g.129528875A>T | CA354495914 | RHO | c.142A>T (p.Ile48Phe) | |
3 | g.129528876T>A | CA354495915 | RHO | c.143T>A (p.Ile48Asn) | |
3 | g.129528876T>C | CA354495918 | RHO | c.143T>C (p.Ile48Thr) | COSMIC |
3 | g.129528876T>G | CA354495916 | RHO | c.143T>G (p.Ile48Ser) | |
3 | g.129528877C>A | CA435768919 | RHO | c.144C>A (p.Ile48=) | gnomAD v4 |
3 | g.129528877C= | CA1401205420 | RHO | c.144C= (p.Ile48=) | |
3 | g.129528877C>G | CA354495921 | RHO | c.144C>G (p.Ile48Met) | gnomAD v4 |
3 | g.129528877C>T | CA2607068 | RHO | c.144C>T (p.Ile48=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129528878G>A | CA2607069 | RHO | c.145G>A (p.Val49Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129528878G>C | CA354495924 | RHO | c.145G>C (p.Val49Leu) | |
3 | g.129528878G= | CA1401205426 | RHO | c.145G= (p.Val49=) | |
3 | g.129528878G>T | CA354495926 | RHO | c.145G>T (p.Val49Leu) | |
3 | g.129528879T>A | CA354495928 | RHO | c.146T>A (p.Val49Glu) | |
3 | g.129528879T>C | CA354495929 | RHO | c.146T>C (p.Val49Ala) | |
3 | g.129528879T>G | CA354495931 | RHO | c.146T>G (p.Val49Gly) | |
3 | g.129528880G>A | CA435768922 | RHO | c.147G>A (p.Val49=) | |
3 | g.129528880G>C | CA435768923 | RHO | c.147G>C (p.Val49=) | |
3 | g.129528880G>T | CA435768924 | RHO | c.147G>T (p.Val49=) |