Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.129532724G>A | CA435769222 | RHO | c.888G>A (p.Lys296=) | ClinVar gnomAD v4 |
3 | g.129532724G>C | CA354470800 | RHO | c.888G>C (p.Lys296Asn) | ClinVar dbSNP |
3 | g.129532724G= | CA1401211995 | RHO | c.888G= (p.Lys296=) | |
3 | g.129532724G>T | CA354470802 | RHO | c.888G>T (p.Lys296Asn) | ClinVar |
3 | g.129532725A>C | CA354470804 | RHO | c.889A>C (p.Ser297Arg) | ClinVar |
3 | g.129532725A>G | CA354470806 | RHO | c.889A>G (p.Ser297Gly) | |
3 | g.129532725A>T | CA354470808 | RHO | c.889A>T (p.Ser297Cys) | |
3 | g.129532726G>A | CA354470810 | RHO | c.890G>A (p.Ser297Asn) | |
3 | g.129532726G>C | CA354470812 | RHO | c.890G>C (p.Ser297Thr) | |
3 | g.129532726G>T | CA354470815 | RHO | c.890G>T (p.Ser297Ile) | |
3 | g.129532727C>A | CA354470817 | RHO | c.891C>A (p.Ser297Arg) | |
3 | g.129532727C= | CA1401212009 | RHO | c.891C= (p.Ser297=) | |
3 | g.129532727C>G | CA354470820 | RHO | c.891C>G (p.Ser297Arg) | ClinVar dbSNP |
3 | g.129532727C>T | CA232817 | RHO | c.891C>T (p.Ser297=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129532728G>A | CA2607302 | RHO | c.892G>A (p.Ala298Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129532728G>C | CA354470829 | RHO | c.892G>C (p.Ala298Pro) | |
3 | g.129532728G= | CA1401212016 | RHO | c.892G= (p.Ala298=) | |
3 | g.129532728G>T | CA354470827 | RHO | c.892G>T (p.Ala298Ser) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.129532729C>A | CA354470834 | RHO | c.893C>A (p.Ala298Asp) | dbSNP |
3 | g.129532729C= | CA1401212023 | RHO | c.893C= (p.Ala298=) | |
3 | g.129532729C>G | CA354470839 | RHO | c.893C>G (p.Ala298Gly) | COSMIC |
3 | g.129532729C>T | CA354470836 | RHO | c.893C>T (p.Ala298Val) | ClinVar |
3 | g.129532730C>A | CA435769223 | RHO | c.894C>A (p.Ala298=) | |
3 | g.129532730C= | CA1401212027 | RHO | c.894C= (p.Ala298=) | |
3 | g.129532730C>G | CA2607304 | RHO | c.894C>G (p.Ala298=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129532730C>T | CA2607303 | RHO | c.894C>T (p.Ala298=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129532731G>A | CA2607306 | RHO | c.895G>A (p.Ala299Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129532731G>C | CA354470847 | RHO | c.895G>C (p.Ala299Pro) | |
3 | g.129532731G= | CA1401212032 | RHO | c.895G= (p.Ala299=) | |
3 | g.129532731G>T | CA2607305 | RHO | c.895G>T (p.Ala299Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129532732C>A | CA354470851 | RHO | c.896C>A (p.Ala299Asp) | |
3 | g.129532732C>G | CA354470854 | RHO | c.896C>G (p.Ala299Gly) | |
3 | g.129532732C>T | CA354470856 | RHO | c.896C>T (p.Ala299Val) | |
3 | g.129532733C>A | CA435769224 | RHO | c.897C>A (p.Ala299=) | |
3 | g.129532733C= | CA1401212038 | RHO | c.897C= (p.Ala299=) | |
3 | g.129532733C>G | CA435769225 | RHO | c.897C>G (p.Ala299=) | |
3 | g.129532733C>T | CA435769226 | RHO | c.897C>T (p.Ala299=) | dbSNP gnomAD v3 gnomAD v4 |
3 | g.129532734A= | CA1401212046 | RHO | c.898A= (p.Ile300=) | |
3 | g.129532734A>C | CA354470859 | RHO | c.898A>C (p.Ile300Leu) | |
3 | g.129532734A>G | CA354470862 | RHO | c.898A>G (p.Ile300Val) | |
3 | g.129532734A>T | CA2607307 | RHO | c.898A>T (p.Ile300Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129532735T>A | CA354470867 | RHO | c.899T>A (p.Ile300Asn) | |
3 | g.129532735T>C | CA354470870 | RHO | c.899T>C (p.Ile300Thr) | |
3 | g.129532735T>G | CA354470872 | RHO | c.899T>G (p.Ile300Ser) | |
3 | g.129532736C>A | CA435769227 | RHO | c.900C>A (p.Ile300=) | gnomAD v4 |
3 | g.129532736C>G | CA354470875 | RHO | c.900C>G (p.Ile300Met) | |
3 | g.129532736C>T | CA435769228 | RHO | c.900C>T (p.Ile300=) | |
3 | g.129532737T>A | CA354470877 | RHO | c.901T>A (p.Tyr301Asn) | |
3 | g.129532737T>C | CA354470883 | RHO | c.901T>C (p.Tyr301His) | |
3 | g.129532737T>G | CA354470880 | RHO | c.901T>G (p.Tyr301Asp) |