Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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=) | |
3 | g.129528881C>A | CA354495932 | RHO | c.148C>A (p.Leu50Met) | |
3 | g.129528881C>G | CA354495933 | RHO | c.148C>G (p.Leu50Val) | |
3 | g.129528881C>T | CA435768925 | RHO | c.148C>T (p.Leu50=) | gnomAD v4 |
3 | g.129528882T>A | CA354495935 | RHO | c.149T>A (p.Leu50Gln) | |
3 | g.129528882T>C | CA354495937 | RHO | c.149T>C (p.Leu50Pro) | dbSNP |
3 | g.129528882T>G | CA354495941 | RHO | c.149T>G (p.Leu50Arg) | |
3 | g.129528882T= | CA1401205436 | RHO | c.149T= (p.Leu50=) | |
3 | g.129528883G>A | CA435768927 | RHO | c.150G>A (p.Leu50=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129528883G>C | CA435768928 | RHO | c.150G>C (p.Leu50=) | |
3 | g.129528883G= | CA1401205443 | RHO | c.150G= (p.Leu50=) | |
3 | g.129528883G>T | CA435768929 | RHO | c.150G>T (p.Leu50=) | |
3 | g.129528884G>A | CA354495942 | RHO | c.151G>A (p.Gly51Ser) | |
3 | g.129528884G>C | CA256687 | RHO | c.151G>C (p.Gly51Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.129528884G= | CA1401205449 | RHO | c.151G= (p.Gly51=) | |
3 | g.129528884G>T | CA354495943 | RHO | c.151G>T (p.Gly51Cys) | dbSNP |
3 | g.129528885G>A | CA354495946 | RHO | c.152G>A (p.Gly51Asp) | |
3 | g.129528885G>C | CA2607070 | RHO | c.152G>C (p.Gly51Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129528885G= | CA1401205458 | RHO | c.152G= (p.Gly51=) | |
3 | g.129528885G>T | CA354495947 | RHO | c.152G>T (p.Gly51Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.129528886C>A | CA435768930 | RHO | c.153C>A (p.Gly51=) | |
3 | g.129528886C>G | CA435768931 | RHO | c.153C>G (p.Gly51=) | |
3 | g.129528886C>T | CA435768932 | RHO | c.153C>T (p.Gly51=) | gnomAD v4 |
3 | g.129528887T>A | CA354495948 | RHO | c.154T>A (p.Phe52Ile) | |
3 | g.129528887T>C | CA82646800 | RHO | c.154T>C (p.Phe52Leu) | dbSNP |
3 | g.129528887T>G | CA354495950 | RHO | c.154T>G (p.Phe52Val) | |
3 | g.129528887T= | CA1401205473 | RHO | c.154T= (p.Phe52=) | |
3 | g.129528888T>A | CA354495952 | RHO | c.155T>A (p.Phe52Tyr) | gnomAD v4 |
3 | g.129528888T>C | CA354495954 | RHO | c.155T>C (p.Phe52Ser) | |
3 | g.129528888T>G | CA354495955 | RHO | c.155T>G (p.Phe52Cys) | |
3 | g.129528889C>A | CA354495958 | RHO | c.156C>A (p.Phe52Leu) |