Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.41741252C>ACA512663066RIPK4c.1941G>T (p.Thr647=)
c.2085G>T (p.Thr695=)
21g.41741252C=CA2390468028RIPK4c.1941G= (p.Thr647=)
c.2085G= (p.Thr695=)
21g.41741252C>GCA512663067RIPK4c.1941G>C (p.Thr647=)
c.2085G>C (p.Thr695=)
21g.41741252C>TCA10035172RIPK4c.1941G>A (p.Thr647=)
c.2085G>A (p.Thr695=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741253G>ACA10035173RIPK4c.1940C>T (p.Thr647Met)
c.2084C>T (p.Thr695Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741253G>CCA410326140RIPK4c.1940C>G (p.Thr647Arg)
c.2084C>G (p.Thr695Arg)
21g.41741253G=CA2390468029RIPK4c.1940C= (p.Thr647=)
c.2084C= (p.Thr695=)
21g.41741253G>TCA410326141RIPK4c.1940C>A (p.Thr647Lys)
c.2084C>A (p.Thr695Lys)
gnomAD v4
21g.41741254T>ACA410326142RIPK4c.1939A>T (p.Thr647Ser)
c.2083A>T (p.Thr695Ser)
21g.41741254T>CCA410326143RIPK4c.1939A>G (p.Thr647Ala)
c.2083A>G (p.Thr695Ala)
gnomAD v4
21g.41741254T>GCA410326144RIPK4c.1939A>C (p.Thr647Pro)
c.2083A>C (p.Thr695Pro)
21g.41741255C>ACA410326145RIPK4c.1938G>T (p.Glu646Asp)
c.2082G>T (p.Glu694Asp)
21g.41741255C>GCA410326146RIPK4c.1938G>C (p.Glu646Asp)
c.2082G>C (p.Glu694Asp)
21g.41741255C>TCA512663073RIPK4c.1938G>A (p.Glu646=)
c.2082G>A (p.Glu694=)
21g.41741256T>ACA410326147RIPK4c.1937A>T (p.Glu646Val)
c.2081A>T (p.Glu694Val)
21g.41741256T>CCA410326148RIPK4c.1937A>G (p.Glu646Gly)
c.2081A>G (p.Glu694Gly)
21g.41741256T>GCA410326149RIPK4c.1937A>C (p.Glu646Ala)
c.2081A>C (p.Glu694Ala)
21g.41741257C>ACA410326150RIPK4c.1936G>T (p.Glu646Ter)
c.2080G>T (p.Glu694Ter)
21g.41741257C>GCA410326152RIPK4c.1936G>C (p.Glu646Gln)
c.2080G>C (p.Glu694Gln)
21g.41741257C>TCA410326151RIPK4c.1936G>A (p.Glu646Lys)
c.2080G>A (p.Glu694Lys)
COSMIC COSMIC
21g.41741258C>ACA512663076RIPK4c.1935G>T (p.Ala645=)
c.2079G>T (p.Ala693=)
21g.41741258C=CA2390468030RIPK4c.1935G= (p.Ala645=)
c.2079G= (p.Ala693=)
21g.41741258C>GCA512663077RIPK4c.1935G>C (p.Ala645=)
c.2079G>C (p.Ala693=)
21g.41741258C>TCA10035174RIPK4c.1935G>A (p.Ala645=)
c.2079G>A (p.Ala693=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741259G>ACA10035175RIPK4c.1934C>T (p.Ala645Val)
c.2078C>T (p.Ala693Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741259G>CCA410326153RIPK4c.1934C>G (p.Ala645Gly)
c.2078C>G (p.Ala693Gly)
21g.41741259G=CA2390468031RIPK4c.1934C= (p.Ala645=)
c.2078C= (p.Ala693=)
21g.41741259G>TCA410326154RIPK4c.1934C>A (p.Ala645Glu)
c.2078C>A (p.Ala693Glu)
gnomAD v4
21g.41741260C>ACA410326155RIPK4c.1933G>T (p.Ala645Ser)
c.2077G>T (p.Ala693Ser)
21g.41741260C=CA2390468032RIPK4c.1933G= (p.Ala645=)
c.2077G= (p.Ala693=)
21g.41741260C>GCA410326156RIPK4c.1933G>C (p.Ala645Pro)
c.2077G>C (p.Ala693Pro)
21g.41741260C>TCA10035176RIPK4c.1933G>A (p.Ala645Thr)
c.2077G>A (p.Ala693Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741261G>ACA10035177RIPK4c.1932C>T (p.Ala644=)
c.2076C>T (p.Ala692=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.41741261G>CCA512663083RIPK4c.1932C>G (p.Ala644=)
c.2076C>G (p.Ala692=)
21g.41741261G=CA2390468033RIPK4c.1932C= (p.Ala644=)
c.2076C= (p.Ala692=)
21g.41741261G>TCA512663085RIPK4c.1932C>A (p.Ala644=)
c.2076C>A (p.Ala692=)
gnomAD v4
21g.41741262G>ACA321453711RIPK4c.1931C>T (p.Ala644Val)
c.2075C>T (p.Ala692Val)
dbSNP gnomAD v4
21g.41741262G>CCA410326157RIPK4c.1931C>G (p.Ala644Gly)
c.2075C>G (p.Ala692Gly)
21g.41741262G=CA2390468034RIPK4c.1931C= (p.Ala644=)
c.2075C= (p.Ala692=)
21g.41741262G>TCA410326158RIPK4c.1931C>A (p.Ala644Asp)
c.2075C>A (p.Ala692Asp)
21g.41741263C>ACA410326160RIPK4c.1930G>T (p.Ala644Ser)
c.2074G>T (p.Ala692Ser)
21g.41741263C=CA2390468035RIPK4c.1930G= (p.Ala644=)
c.2074G= (p.Ala692=)
21g.41741263C>GCA410326159RIPK4c.1930G>C (p.Ala644Pro)
c.2074G>C (p.Ala692Pro)
21g.41741263C>TCA321453716RIPK4c.1930G>A (p.Ala644Thr)
c.2074G>A (p.Ala692Thr)
dbSNP gnomAD v4
21g.41741264C>ACA512663086RIPK4c.1929G>T (p.Val643=)
c.2073G>T (p.Val691=)
21g.41741264C>GCA512663087RIPK4c.1929G>C (p.Val643=)
c.2073G>C (p.Val691=)
gnomAD v4
21g.41741264C>TCA512663088RIPK4c.1929G>A (p.Val643=)
c.2073G>A (p.Val691=)
21g.41741265A>CCA410326161RIPK4c.1928T>G (p.Val643Gly)
c.2072T>G (p.Val691Gly)
21g.41741265A>GCA410326162RIPK4c.1928T>C (p.Val643Ala)
c.2072T>C (p.Val691Ala)
21g.41741265A>TCA410326163RIPK4c.1928T>A (p.Val643Glu)
c.2072T>A (p.Val691Glu)

Number of alleles fetched