Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.41741152C>ACA410325790RIPK4c.2041G>T (p.Gly681Ter)
c.2185G>T (p.Gly729Ter)
21g.41741152C=CA2390467970RIPK4c.2041G= (p.Gly681=)
c.2185G= (p.Gly729=)
21g.41741152C>GCA410325791RIPK4c.2041G>C (p.Gly681Arg)
c.2185G>C (p.Gly729Arg)
gnomAD v4
21g.41741152C>TCA10035149RIPK4c.2041G>A (p.Gly681Arg)
c.2185G>A (p.Gly729Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741153G>ACA10035150RIPK4c.2040C>T (p.Asn680=)
c.2184C>T (p.Asn728=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
21g.41741153G>CCA410325795RIPK4c.2040C>G (p.Asn680Lys)
c.2184C>G (p.Asn728Lys)
21g.41741153G=CA2390467971RIPK4c.2040C= (p.Asn680=)
c.2184C= (p.Asn728=)
21g.41741153G>TCA410325797RIPK4c.2040C>A (p.Asn680Lys)
c.2184C>A (p.Asn728Lys)
21g.41741154T>ACA410325799RIPK4c.2039A>T (p.Asn680Ile)
c.2183A>T (p.Asn728Ile)
21g.41741154T>CCA410325801RIPK4c.2039A>G (p.Asn680Ser)
c.2183A>G (p.Asn728Ser)
dbSNP gnomAD v3 gnomAD v4
21g.41741154T>GCA410325803RIPK4c.2039A>C (p.Asn680Thr)
c.2183A>C (p.Asn728Thr)
21g.41741154T=CA2390467972RIPK4c.2039A= (p.Asn680=)
c.2183A= (p.Asn728=)
21g.41741155dupCA2654631196RIPK4c.2039dup (p.Asn680LysfsTer?)
c.2183dup (p.Asn728LysfsTer?)
gnomAD v4
21g.41741155T>ACA410325804RIPK4c.2038A>T (p.Asn680Tyr)
c.2182A>T (p.Asn728Tyr)
21g.41741155T>CCA410325806RIPK4c.2038A>G (p.Asn680Asp)
c.2182A>G (p.Asn728Asp)
21g.41741155T>GCA410325808RIPK4c.2038A>C (p.Asn680His)
c.2182A>C (p.Asn728His)
21g.41741156G>ACA512662897RIPK4c.2037C>T (p.Arg679=)
c.2181C>T (p.Arg727=)
21g.41741156G>CCA512662895RIPK4c.2037C>G (p.Arg679=)
c.2181C>G (p.Arg727=)
21g.41741156G>TCA512662896RIPK4c.2037C>A (p.Arg679=)
c.2181C>A (p.Arg727=)
21g.41741157C>ACA410325810RIPK4c.2036G>T (p.Arg679Leu)
c.2180G>T (p.Arg727Leu)
dbSNP
21g.41741157C=CA2390467973RIPK4c.2036G= (p.Arg679=)
c.2180G= (p.Arg727=)
21g.41741157C>GCA410325812RIPK4c.2036G>C (p.Arg679Pro)
c.2180G>C (p.Arg727Pro)
21g.41741157C>TCA10035151RIPK4c.2036G>A (p.Arg679His)
c.2180G>A (p.Arg727His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
21g.41741158G>ACA10035152RIPK4c.2035C>T (p.Arg679Cys)
c.2179C>T (p.Arg727Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
21g.41741158G>CCA321453591RIPK4c.2035C>G (p.Arg679Gly)
c.2179C>G (p.Arg727Gly)
dbSNP
21g.41741158G=CA2390467974RIPK4c.2035C= (p.Arg679=)
c.2179C= (p.Arg727=)
21g.41741158G>TCA410325816RIPK4c.2035C>A (p.Arg679Ser)
c.2179C>A (p.Arg727Ser)
21g.41741159G>ACA512662902RIPK4c.2034C>T (p.Ala678=)
c.2178C>T (p.Ala726=)
dbSNP gnomAD v2 gnomAD v4
21g.41741159G>CCA512662900RIPK4c.2034C>G (p.Ala678=)
c.2178C>G (p.Ala726=)
21g.41741159G=CA2390467975RIPK4c.2034C= (p.Ala678=)
c.2178C= (p.Ala726=)
21g.41741159G>TCA512662898RIPK4c.2034C>A (p.Ala678=)
c.2178C>A (p.Ala726=)
gnomAD v4
21g.41741159_41741161delinsGGCCA2390467976RIPK4c.2032_2034delinsGCC (p.Ala678=)
c.2176_2178delinsGCC (p.Ala726=)
21g.41741160G>ACA410325818RIPK4c.2033C>T (p.Ala678Val)
c.2177C>T (p.Ala726Val)
gnomAD v4
21g.41741160G>CCA410325819RIPK4c.2033C>G (p.Ala678Gly)
c.2177C>G (p.Ala726Gly)
21g.41741160G>TCA410325821RIPK4c.2033C>A (p.Ala678Asp)
c.2177C>A (p.Ala726Asp)
gnomAD v4
21g.41741160_41741161delCA920311208RIPK4c.2032_2033del (p.Ala678ProfsTer?)
c.2176_2177del (p.Ala726ProfsTer?)
dbSNP gnomAD v4
21g.41741161C>ACA410325823RIPK4c.2032G>T (p.Ala678Ser)
c.2176G>T (p.Ala726Ser)
gnomAD v4
21g.41741161C=CA2390467977RIPK4c.2032G= (p.Ala678=)
c.2176G= (p.Ala726=)
21g.41741161C>GCA410325825RIPK4c.2032G>C (p.Ala678Pro)
c.2176G>C (p.Ala726Pro)
21g.41741161C>TCA10035153RIPK4c.2032G>A (p.Ala678Thr)
c.2176G>A (p.Ala726Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
21g.41741162A=CA2390467978RIPK4c.2031T= (p.Ala677=)
c.2175T= (p.Ala725=)
21g.41741162A>CCA512662904RIPK4c.2031T>G (p.Ala677=)
c.2175T>G (p.Ala725=)
gnomAD v4
21g.41741162A>GCA512662906RIPK4c.2031T>C (p.Ala677=)
c.2175T>C (p.Ala725=)
21g.41741162A>TCA512662907RIPK4c.2031T>A (p.Ala677=)
c.2175T>A (p.Ala725=)
dbSNP gnomAD v2 gnomAD v4
21g.41741163G>ACA410325828RIPK4c.2030C>T (p.Ala677Val)
c.2174C>T (p.Ala725Val)
dbSNP gnomAD v2
21g.41741163G>CCA410325830RIPK4c.2030C>G (p.Ala677Gly)
c.2174C>G (p.Ala725Gly)
21g.41741163G=CA2390467979RIPK4c.2030C= (p.Ala677=)
c.2174C= (p.Ala725=)
21g.41741163G>TCA410325831RIPK4c.2030C>A (p.Ala677Asp)
c.2174C>A (p.Ala725Asp)
gnomAD v4
21g.41741164C>ACA410325833RIPK4c.2029G>T (p.Ala677Ser)
c.2173G>T (p.Ala725Ser)
gnomAD v4
21g.41741164C>GCA410325834RIPK4c.2029G>C (p.Ala677Pro)
c.2173G>C (p.Ala725Pro)
gnomAD v4

Number of alleles fetched